The Royal Society of Chemistry
Cambridge, Cambridgeshire
Professional Standards Specialist Location : Cambridge - Hybrid Contract Type: Temporary Hours: Full time Salary: £39,925 - £44,359 per annum plus benefits Closing Date: 12/05/2024 The Royal Society of Chemistry (RSC) is seeking a Professional Standards Specialist to join our Qualifications team on a temporary basis covering maternity leave (9-12 months). This is a key role responsible for the project management of professional practice in relation to our members' continuing professional development (CPD) and Chartered status.In this position, you will: • Oversee the promotion of best practices in professional development and training for our members, particularly in supporting the achievement of Chartered designations.• Manage the RSC's portfolio of accredited company schemes, which will involve substantial UK travel and the ability to influence existing and potential customers. This requires interacting with high level contacts at leading multinational companies.• Contribute to the development and advancement of our professional registers, working closely with our Registration Officer.• Play a significant role in delivering our membership and industry strategies through the enhancement of CPD offerings.• In this role it is expected that you will attend the office once a month. The role will require travel across the UK and potentially internationally. If you need flexible working arrangements, please outline this in your application. What we are looking for: • A degree in the chemical sciences• Either membership of the Royal Society (MRSC) of Chemistry and the award of Charted Chemist, or eligibility to apply for these.• A consolidated knowledge of science with developed professional key skills obtained through postgraduate employment.• Some project management experience• The ability to demonstrate an understanding of continuing professional development.• Excellent communication and team building skill. If you are interested in this role, please apply before the end of the closing date. When applying, you will need to provide an up-to-date CV and a supporting statement (no more than 500 words) indicating how your skills/ expertise match the competencies outlined in the Job Description. About the RSC Visit our Work For Us website to learn more about us, our benefits, equal opportunities statement and inclusive culture pledge.At the RSC we embrace flexibility and offer hybrid working, which means our teams come together when they need to collaborate. Although this role is contractually based at our Cambridge office, you will be able to work from home within the UK, with the expectation that you will attend the office as needed for your role. At the RSC, we recognise the benefits of a diverse workforce and welcome applicants from a range of backgrounds to apply. We particularly encourage applications from disabled and ethnic minority candidates. As a part of the Disability Confident Scheme, we endeavour, where possible, to offer an interview to candidates meeting the essential criteria of the role, who has a substantial physical/mental impairment which impacts their ability to carry out day-to-day tasks. We are committed to making our recruitment processes accessible to all and as part of this, we are flexible in the ways we give and receive information. If you would like to apply using a different format, please contact us and we will do our best to put any reasonable adjustments in place. If you have any questions, please contact us. You may also have experience in the following: Professional Standards Coordinator, Professional standards Manager, Scientific Ethics, Regulatory Affairs, SOPs, Process improvement, Risk Management, MRSC, Project Management, Best practice etc REF-
May 01, 2024
Full time
Professional Standards Specialist Location : Cambridge - Hybrid Contract Type: Temporary Hours: Full time Salary: £39,925 - £44,359 per annum plus benefits Closing Date: 12/05/2024 The Royal Society of Chemistry (RSC) is seeking a Professional Standards Specialist to join our Qualifications team on a temporary basis covering maternity leave (9-12 months). This is a key role responsible for the project management of professional practice in relation to our members' continuing professional development (CPD) and Chartered status.In this position, you will: • Oversee the promotion of best practices in professional development and training for our members, particularly in supporting the achievement of Chartered designations.• Manage the RSC's portfolio of accredited company schemes, which will involve substantial UK travel and the ability to influence existing and potential customers. This requires interacting with high level contacts at leading multinational companies.• Contribute to the development and advancement of our professional registers, working closely with our Registration Officer.• Play a significant role in delivering our membership and industry strategies through the enhancement of CPD offerings.• In this role it is expected that you will attend the office once a month. The role will require travel across the UK and potentially internationally. If you need flexible working arrangements, please outline this in your application. What we are looking for: • A degree in the chemical sciences• Either membership of the Royal Society (MRSC) of Chemistry and the award of Charted Chemist, or eligibility to apply for these.• A consolidated knowledge of science with developed professional key skills obtained through postgraduate employment.• Some project management experience• The ability to demonstrate an understanding of continuing professional development.• Excellent communication and team building skill. If you are interested in this role, please apply before the end of the closing date. When applying, you will need to provide an up-to-date CV and a supporting statement (no more than 500 words) indicating how your skills/ expertise match the competencies outlined in the Job Description. About the RSC Visit our Work For Us website to learn more about us, our benefits, equal opportunities statement and inclusive culture pledge.At the RSC we embrace flexibility and offer hybrid working, which means our teams come together when they need to collaborate. Although this role is contractually based at our Cambridge office, you will be able to work from home within the UK, with the expectation that you will attend the office as needed for your role. At the RSC, we recognise the benefits of a diverse workforce and welcome applicants from a range of backgrounds to apply. We particularly encourage applications from disabled and ethnic minority candidates. As a part of the Disability Confident Scheme, we endeavour, where possible, to offer an interview to candidates meeting the essential criteria of the role, who has a substantial physical/mental impairment which impacts their ability to carry out day-to-day tasks. We are committed to making our recruitment processes accessible to all and as part of this, we are flexible in the ways we give and receive information. If you would like to apply using a different format, please contact us and we will do our best to put any reasonable adjustments in place. If you have any questions, please contact us. You may also have experience in the following: Professional Standards Coordinator, Professional standards Manager, Scientific Ethics, Regulatory Affairs, SOPs, Process improvement, Risk Management, MRSC, Project Management, Best practice etc REF-
Reporting to the Head of Quality you will lead and manage the workload and performance of the QC Department ensuring the successful and compliant delivery of team goals, positive KPI improvement and sustainment, whilst maintaining robust Laboratory Management Systems and adhering to regulatory compliance and expected batch release timelines in support of customer expectations. Overseeing and supporting the day-to-day running of the department and allocation of work. Ensure activities within the department are in line with company policy, best practice, and cGMP/GLP compliant. Produce results in line with company policy, best practice and cGMP in the desired timeframes as directed by the business and by their line manager. Facilitate review and approval of change control, OOS/OOT, and deviation records under their control. Overseeing Quality Control activities including. o Batch Testing Management o Incoming material QC and Release o Inspection Readiness for all associated QC aspects o Quality & SHE Risk Management within areas of accountability. o GMP/SHE Training Compliance o Input into Quality Management Review o Regulations Compliance management for QC o Quality Documentation Lifecycle management for QC o Validation and Qualification activities for QC Labs and Equipment. o Retain and Reserve sample management. o Stability or Technical studies under QC control o QC support for NPI and Technology transfer of any new/improved assays Hiring and day-to-day management of people for the QC department The ability to consistently perform and understand the tasks that are the responsibility of the QC Department. With support from the Head of Quality to instigate and manage projects to ensure the business continues to operate to cGMP/GLP. Successfully liaise with members of other departments at all levels to resolve any Quality related issues creating a partnership working environment under the 'Quality at Source' initiative. Create and Perform Lab related training. Liaise with internal and external customers / project managers on QC/Quality matters. Support resource planning and CAPEX for QC Scientific degree (ideally pharmacy, pharmaceutical sciences, biology, chemistry or related). Previous experience in a pharmaceutical or similar industry. Excellent first line management skills. Excellent attention to detail, with the ability to work accurately in a busy and demanding environment. Excellent verbal and technical writing skills with the ability to communicate at all levels. Computer literate in Microsoft Office (i.e. word, excel, outlook, PowerPoint). An excellent awareness of cGMP/GLP best practice and processes. The ability to take a leading role within the team and support a high performing quality/safety minded culture. Have excellent time management/organisational skills to perform their job efficiently; requires minimal input from line management to achieve planning/deadlines. Ability to suggest innovative and practical ideas/solutions to problems while using associated continuous improvement tools and techniques.
May 01, 2024
Full time
Reporting to the Head of Quality you will lead and manage the workload and performance of the QC Department ensuring the successful and compliant delivery of team goals, positive KPI improvement and sustainment, whilst maintaining robust Laboratory Management Systems and adhering to regulatory compliance and expected batch release timelines in support of customer expectations. Overseeing and supporting the day-to-day running of the department and allocation of work. Ensure activities within the department are in line with company policy, best practice, and cGMP/GLP compliant. Produce results in line with company policy, best practice and cGMP in the desired timeframes as directed by the business and by their line manager. Facilitate review and approval of change control, OOS/OOT, and deviation records under their control. Overseeing Quality Control activities including. o Batch Testing Management o Incoming material QC and Release o Inspection Readiness for all associated QC aspects o Quality & SHE Risk Management within areas of accountability. o GMP/SHE Training Compliance o Input into Quality Management Review o Regulations Compliance management for QC o Quality Documentation Lifecycle management for QC o Validation and Qualification activities for QC Labs and Equipment. o Retain and Reserve sample management. o Stability or Technical studies under QC control o QC support for NPI and Technology transfer of any new/improved assays Hiring and day-to-day management of people for the QC department The ability to consistently perform and understand the tasks that are the responsibility of the QC Department. With support from the Head of Quality to instigate and manage projects to ensure the business continues to operate to cGMP/GLP. Successfully liaise with members of other departments at all levels to resolve any Quality related issues creating a partnership working environment under the 'Quality at Source' initiative. Create and Perform Lab related training. Liaise with internal and external customers / project managers on QC/Quality matters. Support resource planning and CAPEX for QC Scientific degree (ideally pharmacy, pharmaceutical sciences, biology, chemistry or related). Previous experience in a pharmaceutical or similar industry. Excellent first line management skills. Excellent attention to detail, with the ability to work accurately in a busy and demanding environment. Excellent verbal and technical writing skills with the ability to communicate at all levels. Computer literate in Microsoft Office (i.e. word, excel, outlook, PowerPoint). An excellent awareness of cGMP/GLP best practice and processes. The ability to take a leading role within the team and support a high performing quality/safety minded culture. Have excellent time management/organisational skills to perform their job efficiently; requires minimal input from line management to achieve planning/deadlines. Ability to suggest innovative and practical ideas/solutions to problems while using associated continuous improvement tools and techniques.
We are currently working exclusively with an international FMCG Group that are seeking to hire a Senior FP&A Manager responsible for commercial project withing the business. This is an exciting opportunity for a technical adept and commercial minded chartered Accountant to make their first move out of practice and into industry. As the business continues to this role will be at the forefront of addressing these challenges/opportunities from a commercial perspective where you will be responsible for delivering mixture of ad-hoc projects and recurring deliverables. STRATEGIC OBJECTIVES AND KEY DELIVERABLES You will be responsible for preparing board level presentations to communicate results, forecasts and annual budgets. Accuracy is non-negotiable. Clarity of messaging to explain performance drivers is where you will add value A key focus will be on delivering ad-hoc projects focused on identifying opportunities to optimize our business and drive performance. You will need to be comfortable working cross-functionally, obtaining insights from stakeholders outside of finance. Financial modelling, communication and insightful analytical skills will all be essential Many of your projects will involve working with and presenting to C-Suite Executives and broader Leadership Team In the medium term opportunities would likely arise to broaden experience in other areas of finance, for example Commercial Finance, Operational Finance or Financial Reporting, as interest/opportunity dictates People development is one of our company's core cultural pillars. This is an ideal role for an ambitious and motivated indivdiual looking to develop the next stage of their career Employees at this level have previously been sponsored to complete certifications in Lean Six Sigma, Anaplan (Business Planning software) and for top performers, MBAs REQUIRED CAPABILITIES To be intellectually curious and to have a continuous improvement mindset to own and fix issues identified A willingness to learn about our business, leaving your desk and spending time in a manufacturing environment To be highly analytical and have an ability to draw insight from large data sets To be an excellent communicator, able to engage and influence stakeholders To be organized and capable of managing multiple activities simultaneously Strong Excel / Power BI skills EDUCATION AND EXPERIENCE REQUIREMENTS Bachelor's degree (minimum 2:1). Technical background preferred (e.g. Engineering, Chemistry, Physics, Maths etc.) Chartered Accountancy, CFA or similar qualification Five years PQE, including time either in an Advisory role such as Transaction Services, Restructuring,Corporate Finance or experience in industry in FP&A or Commercial/Operational Finance WHAT WE OFFER YOU You will be joining a business with an entrepreneurial culture and a flat management structure You will be joining a team that is open, supportive and collegiate We are committed to staff development and career progression (which is on a meritocratic basis) We offer a competitive salary, 26 days holiday, flexible working policies and an industry leading benefits package
May 01, 2024
Full time
We are currently working exclusively with an international FMCG Group that are seeking to hire a Senior FP&A Manager responsible for commercial project withing the business. This is an exciting opportunity for a technical adept and commercial minded chartered Accountant to make their first move out of practice and into industry. As the business continues to this role will be at the forefront of addressing these challenges/opportunities from a commercial perspective where you will be responsible for delivering mixture of ad-hoc projects and recurring deliverables. STRATEGIC OBJECTIVES AND KEY DELIVERABLES You will be responsible for preparing board level presentations to communicate results, forecasts and annual budgets. Accuracy is non-negotiable. Clarity of messaging to explain performance drivers is where you will add value A key focus will be on delivering ad-hoc projects focused on identifying opportunities to optimize our business and drive performance. You will need to be comfortable working cross-functionally, obtaining insights from stakeholders outside of finance. Financial modelling, communication and insightful analytical skills will all be essential Many of your projects will involve working with and presenting to C-Suite Executives and broader Leadership Team In the medium term opportunities would likely arise to broaden experience in other areas of finance, for example Commercial Finance, Operational Finance or Financial Reporting, as interest/opportunity dictates People development is one of our company's core cultural pillars. This is an ideal role for an ambitious and motivated indivdiual looking to develop the next stage of their career Employees at this level have previously been sponsored to complete certifications in Lean Six Sigma, Anaplan (Business Planning software) and for top performers, MBAs REQUIRED CAPABILITIES To be intellectually curious and to have a continuous improvement mindset to own and fix issues identified A willingness to learn about our business, leaving your desk and spending time in a manufacturing environment To be highly analytical and have an ability to draw insight from large data sets To be an excellent communicator, able to engage and influence stakeholders To be organized and capable of managing multiple activities simultaneously Strong Excel / Power BI skills EDUCATION AND EXPERIENCE REQUIREMENTS Bachelor's degree (minimum 2:1). Technical background preferred (e.g. Engineering, Chemistry, Physics, Maths etc.) Chartered Accountancy, CFA or similar qualification Five years PQE, including time either in an Advisory role such as Transaction Services, Restructuring,Corporate Finance or experience in industry in FP&A or Commercial/Operational Finance WHAT WE OFFER YOU You will be joining a business with an entrepreneurial culture and a flat management structure You will be joining a team that is open, supportive and collegiate We are committed to staff development and career progression (which is on a meritocratic basis) We offer a competitive salary, 26 days holiday, flexible working policies and an industry leading benefits package
As an Amazon Worldwide (WW) Workplace Health & Safety (WHS) Methane and Vapor Intrusion Mitigation Specialist and Risk Manager, you will be responsible for all aspects of supporting one of the safest real estate programs in the world! You will partner with various stakeholders and teams around the world to support methane and vapor intrusion mitigation program development and ongoing facility management including standards and policy development, implementation, and execution. To be successful in this role, you will possess exceptional organizational and communication skills and be able to send clear, concise and consistent messages, both verbally and in writing. You will have extensive methane and vapor intrusion experience, mitigation system experience including design, construction, operations, maintenance, and monitoring (OMM), understand the regulatory environment, and demonstrate this expertise when working with internal and external teams. This role will be based in London and requires UK and EU travel 25% of the time. Key job responsibilities Provide a single point of contact to internal and external teams to support them on developing, understanding, and executing Amazon's methane and vapor intrusion programs. Complete due diligence reviews of properties to assess ground gas risk. Complete WHS reviews of mitigation system designs, construction plans, and construction verification, startup testing, and OMM data. Perform system inspections during construction, startup, and operation to evaluate conditions and confirm design and operating assumptions Oversee and direct field personnel providing OMM including developing scopes of work, coordinating and scheduling OMM events, evaluating field reports, and acting-on and implementing follow-up actions. Provide support to a wide range of interested legal, property owner, construction management, preconstruction management, consulting, transaction management, business leadership, and facility operations teams and partners on ground gas risks, methane and vapor intrusion mitigation systems, and OMM. Provide support, training, and feedback to a wide range of consulting, contractors, developers, facility operations teams and partners on methane and vapor intrusion mitigation systems, monitoring equipment, and operations, maintenance, and monitoring plans, programs and performed. We are open to hiring candidates to work out of one of the following locations: London, GBR BASIC QUALIFICATIONS - Bachelor's degree - Experience owning program strategy, end to end delivery, and communicating results to senior leadership - A University Degree in Geology, Environmental Science, Chemistry, Chemical or Environmental Engineering, Civil Engineering, Process Engineering, or related field of study. - Proven experience serving as an environmental technical resource, program specialist, or project manager with a demonstrable focus on methane and vapor intrusion. - Experience in development and implementation of standards, policies, and programs with a demonstrable focus on methane and vapor intrusion. - Possess knowledge and experience regarding the operation, maintenance, and/or monitoring of a variety of methane / vapor intrusion systems (ideally including remote monitoring equipment). - Possess demonstrable knowledge and experience of a variety of UK (and ideally EU) Guidance documents relating to methane and vapor intrusion including (but not limited to) British Standards BS 8576 and BS 8485, CIRIA Reports C682, C735, C748 and C801 etc. - Experience in the development and implementation of standards, policies, and programs. PREFERRED QUALIFICATIONS - The ability to work in a dynamic, changing/growing organization. - The ability to design, oversee construction, and manage methane and vapor intrusion systems internationally. - High levels of interpersonal skills to work effectively with others. - Exceptional organizational skills. - Excellent written and verbal communication skills. - The ability to collaborate with multiple interested parties with a variety of goals and objectives. - The ability to adapt and contribute to evolving approaches for the team. - The ability to manage a high-volume workload with concurrent priorities. - The ability to synthesize large amounts of information into focused conclusions. - Strong analytical and problem-solving skills. - Additional language fluency is a bonus. Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions based on your experience and skills. We value your passion to discover, invent, simplify and build. Protecting your privacy and the security of your data is a longstanding top priority for Amazon. Please consult our Privacy Notice () to know more about how we collect, use and transfer the personal data of our candidates. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need an adjustment during the application and hiring process, including support for the interview or onboarding process, please contact the Applicant-Candidate Accommodation Team (ACAT), Monday through Friday from 7:00 am GMT - 4:00 pm GMT. If calling directly from the United Kingdom, please dial (tel:). If calling from Ireland, please dial (tel:).
May 01, 2024
Full time
As an Amazon Worldwide (WW) Workplace Health & Safety (WHS) Methane and Vapor Intrusion Mitigation Specialist and Risk Manager, you will be responsible for all aspects of supporting one of the safest real estate programs in the world! You will partner with various stakeholders and teams around the world to support methane and vapor intrusion mitigation program development and ongoing facility management including standards and policy development, implementation, and execution. To be successful in this role, you will possess exceptional organizational and communication skills and be able to send clear, concise and consistent messages, both verbally and in writing. You will have extensive methane and vapor intrusion experience, mitigation system experience including design, construction, operations, maintenance, and monitoring (OMM), understand the regulatory environment, and demonstrate this expertise when working with internal and external teams. This role will be based in London and requires UK and EU travel 25% of the time. Key job responsibilities Provide a single point of contact to internal and external teams to support them on developing, understanding, and executing Amazon's methane and vapor intrusion programs. Complete due diligence reviews of properties to assess ground gas risk. Complete WHS reviews of mitigation system designs, construction plans, and construction verification, startup testing, and OMM data. Perform system inspections during construction, startup, and operation to evaluate conditions and confirm design and operating assumptions Oversee and direct field personnel providing OMM including developing scopes of work, coordinating and scheduling OMM events, evaluating field reports, and acting-on and implementing follow-up actions. Provide support to a wide range of interested legal, property owner, construction management, preconstruction management, consulting, transaction management, business leadership, and facility operations teams and partners on ground gas risks, methane and vapor intrusion mitigation systems, and OMM. Provide support, training, and feedback to a wide range of consulting, contractors, developers, facility operations teams and partners on methane and vapor intrusion mitigation systems, monitoring equipment, and operations, maintenance, and monitoring plans, programs and performed. We are open to hiring candidates to work out of one of the following locations: London, GBR BASIC QUALIFICATIONS - Bachelor's degree - Experience owning program strategy, end to end delivery, and communicating results to senior leadership - A University Degree in Geology, Environmental Science, Chemistry, Chemical or Environmental Engineering, Civil Engineering, Process Engineering, or related field of study. - Proven experience serving as an environmental technical resource, program specialist, or project manager with a demonstrable focus on methane and vapor intrusion. - Experience in development and implementation of standards, policies, and programs with a demonstrable focus on methane and vapor intrusion. - Possess knowledge and experience regarding the operation, maintenance, and/or monitoring of a variety of methane / vapor intrusion systems (ideally including remote monitoring equipment). - Possess demonstrable knowledge and experience of a variety of UK (and ideally EU) Guidance documents relating to methane and vapor intrusion including (but not limited to) British Standards BS 8576 and BS 8485, CIRIA Reports C682, C735, C748 and C801 etc. - Experience in the development and implementation of standards, policies, and programs. PREFERRED QUALIFICATIONS - The ability to work in a dynamic, changing/growing organization. - The ability to design, oversee construction, and manage methane and vapor intrusion systems internationally. - High levels of interpersonal skills to work effectively with others. - Exceptional organizational skills. - Excellent written and verbal communication skills. - The ability to collaborate with multiple interested parties with a variety of goals and objectives. - The ability to adapt and contribute to evolving approaches for the team. - The ability to manage a high-volume workload with concurrent priorities. - The ability to synthesize large amounts of information into focused conclusions. - Strong analytical and problem-solving skills. - Additional language fluency is a bonus. Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions based on your experience and skills. We value your passion to discover, invent, simplify and build. Protecting your privacy and the security of your data is a longstanding top priority for Amazon. Please consult our Privacy Notice () to know more about how we collect, use and transfer the personal data of our candidates. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need an adjustment during the application and hiring process, including support for the interview or onboarding process, please contact the Applicant-Candidate Accommodation Team (ACAT), Monday through Friday from 7:00 am GMT - 4:00 pm GMT. If calling directly from the United Kingdom, please dial (tel:). If calling from Ireland, please dial (tel:).
If you are a Jazz employee please apply via the Internal Career site Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage development, in neuroscience and oncology. We actively explore new options for patients including novel compounds, small molecules and biologics, and through cannabinoid science and innovative delivery technologies. Jazz is headquartered in Dublin, Ireland and has employees around the globe, serving patients in nearly 75 countries. For more information, please visit and on Twitter. Brief Description: The Discovery and Medicinal Chemistry Department at Jazz Pharma is seeking an enthusiastic scientist to join the Preformulation & Biopharmaceutics at the Kent Science Park site in Sittingbourne. You will work together with other CMC scientists to advance drug candidates from lead optimization to proof of concept. This role designs and executes elaborate experiments for pharmaceutical sciences projects and demonstrates resourcefulness in running multiple activities concurrently, all related to achievement of goals/objectives. Essential Functions/Responsibilities Collaborate within CMC and cross-functional teams as the pre-Formulation lead and actively contribute to deliverables and engage in cross-functional technical review and troubleshooting. Deliver and oversee the optimization of pre-clinical and clinical formulations through rational experimental design, thoughtful execution, and clear data interpretation. Carry out solubility and dissolution experiment to assess the stability and predict the bio-performance of our internal formulations. Identify gaps in internal formulation/biopharmaceutics capabilities and where appropriate lead an effort to implement suitable technologies. Independently set up solid-form and/or drug product related specifications for CoA Manage, coach and mentor more junior members of staff. Provide clear scientific and technological leadership to direct reports. Comply with all relevant safety and GxP procedures. Plan and prioritise own, and team's work with input from senior manager when required. Involve in CRO's selection process. Provide an oversight of the partnership Required Knowledge, Skills, and Abilities Keep updated of current literature and recent advancements in Biopharmaceutics and Formulation technologies and instrumentation. Knowledge of the interlink between drug substance crystallisation process, material characteristics and impact on drug product development. Good knowledge of pharmacology/DMPK/Tox principles and able to support these areas from drug product perspective. Able to interpret complex technical data. Good knowledge of statistical design of experiments. Team player, able to communicate clearly (excellent writing and presentational skills) Strong knowledge and hands-on experience in drug substance/ drug product characterization is a plus. Knowledge in in silico physiologically-based pharmaceutical models to predict in vivo performance of intravenous and oral formulations is a plus Knowledge of relevant FDA and EMA regulations is a plus. Required/Preferred Education and Licenses PhD/ Master's/ Bachelor's degree in Pharmaceutical Sciences, Chemistry, Material Sciences or Chemical Engineering, with 4- 6 years relevant industrial experience. Jazz Pharmaceuticals is an Equal Opportunity Employer.
May 01, 2024
Full time
If you are a Jazz employee please apply via the Internal Career site Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage development, in neuroscience and oncology. We actively explore new options for patients including novel compounds, small molecules and biologics, and through cannabinoid science and innovative delivery technologies. Jazz is headquartered in Dublin, Ireland and has employees around the globe, serving patients in nearly 75 countries. For more information, please visit and on Twitter. Brief Description: The Discovery and Medicinal Chemistry Department at Jazz Pharma is seeking an enthusiastic scientist to join the Preformulation & Biopharmaceutics at the Kent Science Park site in Sittingbourne. You will work together with other CMC scientists to advance drug candidates from lead optimization to proof of concept. This role designs and executes elaborate experiments for pharmaceutical sciences projects and demonstrates resourcefulness in running multiple activities concurrently, all related to achievement of goals/objectives. Essential Functions/Responsibilities Collaborate within CMC and cross-functional teams as the pre-Formulation lead and actively contribute to deliverables and engage in cross-functional technical review and troubleshooting. Deliver and oversee the optimization of pre-clinical and clinical formulations through rational experimental design, thoughtful execution, and clear data interpretation. Carry out solubility and dissolution experiment to assess the stability and predict the bio-performance of our internal formulations. Identify gaps in internal formulation/biopharmaceutics capabilities and where appropriate lead an effort to implement suitable technologies. Independently set up solid-form and/or drug product related specifications for CoA Manage, coach and mentor more junior members of staff. Provide clear scientific and technological leadership to direct reports. Comply with all relevant safety and GxP procedures. Plan and prioritise own, and team's work with input from senior manager when required. Involve in CRO's selection process. Provide an oversight of the partnership Required Knowledge, Skills, and Abilities Keep updated of current literature and recent advancements in Biopharmaceutics and Formulation technologies and instrumentation. Knowledge of the interlink between drug substance crystallisation process, material characteristics and impact on drug product development. Good knowledge of pharmacology/DMPK/Tox principles and able to support these areas from drug product perspective. Able to interpret complex technical data. Good knowledge of statistical design of experiments. Team player, able to communicate clearly (excellent writing and presentational skills) Strong knowledge and hands-on experience in drug substance/ drug product characterization is a plus. Knowledge in in silico physiologically-based pharmaceutical models to predict in vivo performance of intravenous and oral formulations is a plus Knowledge of relevant FDA and EMA regulations is a plus. Required/Preferred Education and Licenses PhD/ Master's/ Bachelor's degree in Pharmaceutical Sciences, Chemistry, Material Sciences or Chemical Engineering, with 4- 6 years relevant industrial experience. Jazz Pharmaceuticals is an Equal Opportunity Employer.
Project Manager £40,000 - £50,000 + Technical Training + Progression + Benefits Ilkeston, East Midlands (Commutable from: Nottingham, Derby, Heanor, Beeston, West Bridgford, Ripley, Loughborough, Kegworth, Bingham) Are you a Project Manager from an Engineering or Construction background looking to work for a nationally-renowned business who are offering the opportunity to autonomously lead, improve and develop exciting projects within their sole purpose built facility? This is a great opportunity to develop your technical abilities and project management experience where you will be giving further training and mentorship alongside the support of external qualifications. This company are the national leaders within their industry trading as experts. They support a range of Manufacturing and Engineering business through innovative processing techniques. Within this role, you will play a pivotal role in company success through ensuring project tasks are scheduled, prioritised, and planned to ensure safe and efficient outcomes. This will be based out of a huge industrial plant containing high-end machinery. This role would suit a Project Engineer looking to take the next step in their career whilst receiving various development opportunities and an array of company benefits. The Role - Management, lead and development of projects. Focused around HSE policy and improvements. Monday - Friday - occassional travel required. The Person - Project Manager. SMSTS, IOSH, NEBOS or similar qualifications. Engineering or Construction background. To apply for this role or to be considered for further roles, please click "Apply Now" or contact Jamie Davies at Rise Technical Recruitment.Rise Technical Recruitment Ltd acts an employment agency for permanent roles and an employment business for temporary roles.The salary advertised is the bracket available for this position. The actual salary paid will be dependent on your level of experience, qualifications and skill set. We are an equal opportunities employer and welcome applications from all suitable candidates. HSE, Health and Safety, Environmental, Policies, Project Engineer, Project Management, Manager, Engineering, Plant, Machinery, Tanks, Chemical, Chemistry, Projects, Manufacturing, Manufacture.
May 01, 2024
Full time
Project Manager £40,000 - £50,000 + Technical Training + Progression + Benefits Ilkeston, East Midlands (Commutable from: Nottingham, Derby, Heanor, Beeston, West Bridgford, Ripley, Loughborough, Kegworth, Bingham) Are you a Project Manager from an Engineering or Construction background looking to work for a nationally-renowned business who are offering the opportunity to autonomously lead, improve and develop exciting projects within their sole purpose built facility? This is a great opportunity to develop your technical abilities and project management experience where you will be giving further training and mentorship alongside the support of external qualifications. This company are the national leaders within their industry trading as experts. They support a range of Manufacturing and Engineering business through innovative processing techniques. Within this role, you will play a pivotal role in company success through ensuring project tasks are scheduled, prioritised, and planned to ensure safe and efficient outcomes. This will be based out of a huge industrial plant containing high-end machinery. This role would suit a Project Engineer looking to take the next step in their career whilst receiving various development opportunities and an array of company benefits. The Role - Management, lead and development of projects. Focused around HSE policy and improvements. Monday - Friday - occassional travel required. The Person - Project Manager. SMSTS, IOSH, NEBOS or similar qualifications. Engineering or Construction background. To apply for this role or to be considered for further roles, please click "Apply Now" or contact Jamie Davies at Rise Technical Recruitment.Rise Technical Recruitment Ltd acts an employment agency for permanent roles and an employment business for temporary roles.The salary advertised is the bracket available for this position. The actual salary paid will be dependent on your level of experience, qualifications and skill set. We are an equal opportunities employer and welcome applications from all suitable candidates. HSE, Health and Safety, Environmental, Policies, Project Engineer, Project Management, Manager, Engineering, Plant, Machinery, Tanks, Chemical, Chemistry, Projects, Manufacturing, Manufacture.
Hello. We're Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we're improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands - including Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum - through a unique combination of deep human understanding and trusted science. What's more, we're achieving it in a company that we're in control of. In an environment that we're co-creating. And a culture that's uniquely ours. Care to join us. It isn't a question. With category leading brands such as Panadol, Voltaren and Centrum, built on trusted science and human understanding, and combined with our passion, knowledge and expertise, we're uniquely placed to do this and to grow a strong, successful business. This is an exciting time to join us and help shape the future. It's an opportunity to be part of something special. About the role As Quality Assurance Specialist, you will implement and maintain effective Quality Assurance systems to ensure that local operations are in full compliance with Haleon standards and policies, GMP, GDP and regulatory requirements by performing the following: Batch Certification, Release to the Market and repacking activities - Support the batch assessment/release process within the regulatory and corporate framework to ensure timely release of products (medicines, and Mass market products) and timely review of PPR (PQR). Quality Agreements - support review and approval of Technical Terms of Supply or Quality Agreement when required. Management of 3rd Party Contractors - Provide support in third parties overview. Risk Management - Support Risk Management oversight for Quality and supply chain risks. Training - Assign trainings to relevant personnel, KPI monitoring and drive action plans when needed, ensure training matrix and curricula are maintained. QMS implementation - Support QMS implementation strategy, assist in documentation assessment, review and update in timely manner, and relevant personnel are assigned training. Complaint Management - Support the complaint process by ensuring the complaints raised are dealt with in timely manner and assist with trending. NPI - Support the New Product Introduction projects as per as Haleon procedure Customer Qualification - Perform customers qualified and Bonafides when required. Distribution - Assist in distribution issues and returns management from warehouses. Review and confirm Returns and RP/RPI checks delegated to 3rd LSP. Others - Support the team in projects and day to day activities as required such as incident management, PIRC, Internal Audits, Quality Council and Quality team meetings. This is hybrid role out of our offices in London and/or Weybridge (UK) Qualifications and skills Essential Quality experience within the industry, and application of Quality Systems & Quality Operations Minimum of 2-3 years' experience within the Pharmaceutical / Consumer Healthcare Industries, preferably in quality department, experience in a pharmaceutical manufacturing site is required. Knowledge of GMP and GDP regulations and MHRA/HPRA regulation Preferred Experience in importation/distribution of medicines in UK Degree of Pharmacy/Biology/Chemistry of similar Ability to work under pressure, prioritize and manage workload, manage simultaneous tasks, and meet deadlines in a changing, fast-paced environment Care to join us. Find out what life at Haleon is really like At Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone. We're striving to create a climate where we celebrate our diversity in all forms by treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. As you apply, we will ask you to share some personal information, which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially. Haleon is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, Haleon may be required to capture and report expenses Haleon incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure Haleon's compliance to all federal and state US Transparency requirements.
May 01, 2024
Full time
Hello. We're Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we're improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands - including Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum - through a unique combination of deep human understanding and trusted science. What's more, we're achieving it in a company that we're in control of. In an environment that we're co-creating. And a culture that's uniquely ours. Care to join us. It isn't a question. With category leading brands such as Panadol, Voltaren and Centrum, built on trusted science and human understanding, and combined with our passion, knowledge and expertise, we're uniquely placed to do this and to grow a strong, successful business. This is an exciting time to join us and help shape the future. It's an opportunity to be part of something special. About the role As Quality Assurance Specialist, you will implement and maintain effective Quality Assurance systems to ensure that local operations are in full compliance with Haleon standards and policies, GMP, GDP and regulatory requirements by performing the following: Batch Certification, Release to the Market and repacking activities - Support the batch assessment/release process within the regulatory and corporate framework to ensure timely release of products (medicines, and Mass market products) and timely review of PPR (PQR). Quality Agreements - support review and approval of Technical Terms of Supply or Quality Agreement when required. Management of 3rd Party Contractors - Provide support in third parties overview. Risk Management - Support Risk Management oversight for Quality and supply chain risks. Training - Assign trainings to relevant personnel, KPI monitoring and drive action plans when needed, ensure training matrix and curricula are maintained. QMS implementation - Support QMS implementation strategy, assist in documentation assessment, review and update in timely manner, and relevant personnel are assigned training. Complaint Management - Support the complaint process by ensuring the complaints raised are dealt with in timely manner and assist with trending. NPI - Support the New Product Introduction projects as per as Haleon procedure Customer Qualification - Perform customers qualified and Bonafides when required. Distribution - Assist in distribution issues and returns management from warehouses. Review and confirm Returns and RP/RPI checks delegated to 3rd LSP. Others - Support the team in projects and day to day activities as required such as incident management, PIRC, Internal Audits, Quality Council and Quality team meetings. This is hybrid role out of our offices in London and/or Weybridge (UK) Qualifications and skills Essential Quality experience within the industry, and application of Quality Systems & Quality Operations Minimum of 2-3 years' experience within the Pharmaceutical / Consumer Healthcare Industries, preferably in quality department, experience in a pharmaceutical manufacturing site is required. Knowledge of GMP and GDP regulations and MHRA/HPRA regulation Preferred Experience in importation/distribution of medicines in UK Degree of Pharmacy/Biology/Chemistry of similar Ability to work under pressure, prioritize and manage workload, manage simultaneous tasks, and meet deadlines in a changing, fast-paced environment Care to join us. Find out what life at Haleon is really like At Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone. We're striving to create a climate where we celebrate our diversity in all forms by treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. As you apply, we will ask you to share some personal information, which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially. Haleon is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, Haleon may be required to capture and report expenses Haleon incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure Haleon's compliance to all federal and state US Transparency requirements.
Hello. We're Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we're improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands - including Sensodyne, Panadol, Advil, Voltaren , Theraflu, Otrivin , and Centrum - through a unique combination of deep human understanding and trusted science. What's more, we're achieving it in a company that we're in control of. In an environment that we're co-creating. And a culture that's uniquely ours. Care to join us. It isn't a question. With category leading brands such as Sensodyne, Voltaren and Centrum, built on trusted science and human understanding, and combined with our passion, knowledge and expertise , we're uniquely placed to do this and to grow a strong, successful business. This is an exciting time to join us and help shape the future. It's an opportunity to be part of something special. About the role The Future Horizons Product + Senior Scientist is a key member of the Product+ Platform and exists to drive the key prioritized activities across the Product+vertical in digital therapeutics and diagnostics to support driving forward the science & technology partnerships, support and enable the product+ vertical to deliver key solutions and opportunities for proof of interest and proof of science key milestones leading to engagement with Categories/BUs and potential Gate 1 integration. The Project Senior scientist curates the Product+ learnings/portfolio for transfer as required/decided to BUs/Categories. Role Responsibilities PRODUCT+ PROJECT PORTFOLIO: b uilds, drives, and delivers key milestones in moving chosen product+ activities forward and translates portfolio into stakeholder engagement for Categories/BUs PRODUCT+ TRANSFER PACKS: Promotes sharing and reapplying of best practices. Supports communication internally and externally to build program e deliverables and credibility / thought leadership PRODUCT+ EXTERNAL RADAR: Builds, engages, and nurtures with internal and external networks to create early signal radar on new science & technology relevant for rapid milestone progressing within the Product+ vertical. Why you? Basic Qualifications: Bachelor of Science - Chemistry, Pharmacy, Pharmacology, Biochemistry or Biological science 5+ years in FMCG or Healthcare Experience in science & Technology management/partnerships Excellent analytical skills, including strategic thinking Communication and influencing skills, ability to lead change Commercially savvy Care to join us. Find out what life at Haleon is really like At Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone. We're striving to create a climate where we celebrate our diversity in all forms by treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. As you apply, we will ask you to share some personal information, which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially. Haleon is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, Haleon may be required to capture and report expenses Haleon incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure Haleon's compliance to all federal and state US Transparency requirements.
May 01, 2024
Full time
Hello. We're Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we're improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands - including Sensodyne, Panadol, Advil, Voltaren , Theraflu, Otrivin , and Centrum - through a unique combination of deep human understanding and trusted science. What's more, we're achieving it in a company that we're in control of. In an environment that we're co-creating. And a culture that's uniquely ours. Care to join us. It isn't a question. With category leading brands such as Sensodyne, Voltaren and Centrum, built on trusted science and human understanding, and combined with our passion, knowledge and expertise , we're uniquely placed to do this and to grow a strong, successful business. This is an exciting time to join us and help shape the future. It's an opportunity to be part of something special. About the role The Future Horizons Product + Senior Scientist is a key member of the Product+ Platform and exists to drive the key prioritized activities across the Product+vertical in digital therapeutics and diagnostics to support driving forward the science & technology partnerships, support and enable the product+ vertical to deliver key solutions and opportunities for proof of interest and proof of science key milestones leading to engagement with Categories/BUs and potential Gate 1 integration. The Project Senior scientist curates the Product+ learnings/portfolio for transfer as required/decided to BUs/Categories. Role Responsibilities PRODUCT+ PROJECT PORTFOLIO: b uilds, drives, and delivers key milestones in moving chosen product+ activities forward and translates portfolio into stakeholder engagement for Categories/BUs PRODUCT+ TRANSFER PACKS: Promotes sharing and reapplying of best practices. Supports communication internally and externally to build program e deliverables and credibility / thought leadership PRODUCT+ EXTERNAL RADAR: Builds, engages, and nurtures with internal and external networks to create early signal radar on new science & technology relevant for rapid milestone progressing within the Product+ vertical. Why you? Basic Qualifications: Bachelor of Science - Chemistry, Pharmacy, Pharmacology, Biochemistry or Biological science 5+ years in FMCG or Healthcare Experience in science & Technology management/partnerships Excellent analytical skills, including strategic thinking Communication and influencing skills, ability to lead change Commercially savvy Care to join us. Find out what life at Haleon is really like At Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone. We're striving to create a climate where we celebrate our diversity in all forms by treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. As you apply, we will ask you to share some personal information, which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially. Haleon is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, Haleon may be required to capture and report expenses Haleon incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure Haleon's compliance to all federal and state US Transparency requirements.
Job title: Engineering Manager - Nuclear Location: Barrow-in-Furness. We offer a range of hybrid and flexible working arrangements - please speak to your recruiter about the options for this particular role Salary: Competitive What you'll be doing: To develop and maintain safety commissioning management arrangements to deliver the Naval Reactor Plant To deliver a Safety Commissioning Schedule to enable safe delivery of the Naval Reactor Plant Assessing plant safety commissioning maturity for entry into subsequent build phases Facilitating the Reactor Plant build and commissioning delivery programme through innovative engineering solutions and problem solving To lead or support the resolution of safety commissioning challenges Advise and conduct Intelligent Customer duties regarding documentation, advice and services provided to the business relating to safety commissioning of the plant Produce the Safety Commissioning compliance and assurance reports to support the safety case Support the development of the team through mentorship and guidance Writing and presenting reports to communicate nuclear safety matters to a variety of internal and external stakeholders Your skills and experiences: Essential: Degree Qualified Engineering/Physical Science discipline; Electrical, Mechanical, Nuclear, Materials, Chemistry, Physics Knowledge of the nuclear industry and Nuclear Regulations Previous exposure to Engineering Lifecycle Proven experience of demonstrating safety commissioning compliance a Nuclear plant Desirable: Proven technical report writing skills Presentation skills Benefits: You'll receive benefits including a competitive pension scheme, enhanced annual leave allowance and a Company contributed Share Incentive Plan. You'll also have access to additional benefits such as flexible working, an employee assistance programme, Cycle2work and employee discounts - you may also be eligible for an annual incentive. The Platform Nuclear Engineering team: The Platform Nuclear Engineering Department is a growing capability to accommodate the growing Nuclear Engineering demand on the business as the shipyard takes on an unprecedented challenge of delivering multiple classes of Naval Reactor Plant. The team covers activities ranging from design safety assurance, engineering/technical problem solving to practical innovation and improvement projects across the Engineering Lifecycle with a strong focus on the Build and Commission of the reactor plant. There is ample opportunity for professional development and career progression. Why BAE Systems? This is a place where you'll be able to make a real difference. You'll be part of an inclusive culture that values diversity, rewards integrity, and merit, and where you'll be empowered to fulfil your potential. We welcome candidates from all backgrounds and particularly from sections of the community who are currently underrepresented within our industry, including women, ethnic minorities, people with disabilities and LGBTQ+ individuals. We also want to make sure that our recruitment processes are as inclusive as possible. If you have a disability or health condition (for example dyslexia, autism, an anxiety disorder etc.) that may affect your performance in certain assessment types, please speak to your recruiter about potential reasonable adjustments. Please be aware that many roles working for BAE Systems will be subject to both security and export control restrictions. These restrictions mean that factors including your nationality, any previous nationalities you have held, and your place of birth may limit those roles you can perform for the organisation.
May 01, 2024
Full time
Job title: Engineering Manager - Nuclear Location: Barrow-in-Furness. We offer a range of hybrid and flexible working arrangements - please speak to your recruiter about the options for this particular role Salary: Competitive What you'll be doing: To develop and maintain safety commissioning management arrangements to deliver the Naval Reactor Plant To deliver a Safety Commissioning Schedule to enable safe delivery of the Naval Reactor Plant Assessing plant safety commissioning maturity for entry into subsequent build phases Facilitating the Reactor Plant build and commissioning delivery programme through innovative engineering solutions and problem solving To lead or support the resolution of safety commissioning challenges Advise and conduct Intelligent Customer duties regarding documentation, advice and services provided to the business relating to safety commissioning of the plant Produce the Safety Commissioning compliance and assurance reports to support the safety case Support the development of the team through mentorship and guidance Writing and presenting reports to communicate nuclear safety matters to a variety of internal and external stakeholders Your skills and experiences: Essential: Degree Qualified Engineering/Physical Science discipline; Electrical, Mechanical, Nuclear, Materials, Chemistry, Physics Knowledge of the nuclear industry and Nuclear Regulations Previous exposure to Engineering Lifecycle Proven experience of demonstrating safety commissioning compliance a Nuclear plant Desirable: Proven technical report writing skills Presentation skills Benefits: You'll receive benefits including a competitive pension scheme, enhanced annual leave allowance and a Company contributed Share Incentive Plan. You'll also have access to additional benefits such as flexible working, an employee assistance programme, Cycle2work and employee discounts - you may also be eligible for an annual incentive. The Platform Nuclear Engineering team: The Platform Nuclear Engineering Department is a growing capability to accommodate the growing Nuclear Engineering demand on the business as the shipyard takes on an unprecedented challenge of delivering multiple classes of Naval Reactor Plant. The team covers activities ranging from design safety assurance, engineering/technical problem solving to practical innovation and improvement projects across the Engineering Lifecycle with a strong focus on the Build and Commission of the reactor plant. There is ample opportunity for professional development and career progression. Why BAE Systems? This is a place where you'll be able to make a real difference. You'll be part of an inclusive culture that values diversity, rewards integrity, and merit, and where you'll be empowered to fulfil your potential. We welcome candidates from all backgrounds and particularly from sections of the community who are currently underrepresented within our industry, including women, ethnic minorities, people with disabilities and LGBTQ+ individuals. We also want to make sure that our recruitment processes are as inclusive as possible. If you have a disability or health condition (for example dyslexia, autism, an anxiety disorder etc.) that may affect your performance in certain assessment types, please speak to your recruiter about potential reasonable adjustments. Please be aware that many roles working for BAE Systems will be subject to both security and export control restrictions. These restrictions mean that factors including your nationality, any previous nationalities you have held, and your place of birth may limit those roles you can perform for the organisation.
Who we are Tradebe is a group of industrial businesses with the commitment of creating a more sustainable planet and making significant contributions to human wellbeing. Our main business line Tradebe Environmental Services is an international leader focused on recycling, energy recovery and circular economy, managing all different environmental liabilities in a sustainable way. We provide services to the entire industrial complex with high safety and quality standards. Tradebe Inutec has supported the UK's decommissioning mission for 35 years and we continue to develop new treatment and processing solutions to help our customers tackle challenging wastes in a way that benefits our customers and the environment. At our Winfrith nuclear licensed site, we have the most extensive UK & overseas authorisations and safety case of any UK commercial company. Our suitably qualified & experienced personnel provide unrivalled insight and practical experience for radioactive waste treatment services ranging from radiochemistry, treatment, encapsulation, size reduction, incineration, through to disposal. This gives us unparalleled scope and ability to provide innovative and integrated solutions to complex waste projects. We are looking for a hands on Project Scientist working on decontamination and radiological inventory management for our site in Winfrith, Dorset. The role To support the bidding process for and to deliver the technical aspects of radioactive waste management projects for nuclear and industrial clients using professional scientific, engineering and project management principles. Work alongside project manager and engineering teams to help guide tactical and strategic product decisions Support the basic aspects of testing project including equipment preparation, deployment, staging/breakdown, and sampling tasks assigned to them Follow current standards, codes, and procedures regarding safe and effective use of equipment, maintenance programs and other policies Submit reports, technical data, time sheets and project expense reports Work with line managers to secure & develop resources required to deliver tasks Utilise appropriate tools and software to provide required technical information for projects Ensure the relevant project risks are identified and managed / mitigated as appropriate The person Qualified to degree level in a relevant Nuclear Science or Nuclear Engineering Discipline is essential. Attention to detail and ability to question Good interpersonal skills Good written, presentation and verbal communication skills Be able to work under specified and agreed time constraints Professional and positive approach Self-motivated Strong in building relationships and able to communicate at all levels Team player and able to work under own initiative Dynamic and creative and ability to offer solutions Strong customer service priorities Ability to influence cross-functional teams We offer Salary of up to £50,000 per annum Annual bonus Potential for overtime for out of core hours working/TOIL Pension Flexible benefits (access to our benefits platform for discounts and cash back on shopping purchases, gyms and leisure activities, cycle to work scheme and dedicated wellbeing centre)?
May 01, 2024
Full time
Who we are Tradebe is a group of industrial businesses with the commitment of creating a more sustainable planet and making significant contributions to human wellbeing. Our main business line Tradebe Environmental Services is an international leader focused on recycling, energy recovery and circular economy, managing all different environmental liabilities in a sustainable way. We provide services to the entire industrial complex with high safety and quality standards. Tradebe Inutec has supported the UK's decommissioning mission for 35 years and we continue to develop new treatment and processing solutions to help our customers tackle challenging wastes in a way that benefits our customers and the environment. At our Winfrith nuclear licensed site, we have the most extensive UK & overseas authorisations and safety case of any UK commercial company. Our suitably qualified & experienced personnel provide unrivalled insight and practical experience for radioactive waste treatment services ranging from radiochemistry, treatment, encapsulation, size reduction, incineration, through to disposal. This gives us unparalleled scope and ability to provide innovative and integrated solutions to complex waste projects. We are looking for a hands on Project Scientist working on decontamination and radiological inventory management for our site in Winfrith, Dorset. The role To support the bidding process for and to deliver the technical aspects of radioactive waste management projects for nuclear and industrial clients using professional scientific, engineering and project management principles. Work alongside project manager and engineering teams to help guide tactical and strategic product decisions Support the basic aspects of testing project including equipment preparation, deployment, staging/breakdown, and sampling tasks assigned to them Follow current standards, codes, and procedures regarding safe and effective use of equipment, maintenance programs and other policies Submit reports, technical data, time sheets and project expense reports Work with line managers to secure & develop resources required to deliver tasks Utilise appropriate tools and software to provide required technical information for projects Ensure the relevant project risks are identified and managed / mitigated as appropriate The person Qualified to degree level in a relevant Nuclear Science or Nuclear Engineering Discipline is essential. Attention to detail and ability to question Good interpersonal skills Good written, presentation and verbal communication skills Be able to work under specified and agreed time constraints Professional and positive approach Self-motivated Strong in building relationships and able to communicate at all levels Team player and able to work under own initiative Dynamic and creative and ability to offer solutions Strong customer service priorities Ability to influence cross-functional teams We offer Salary of up to £50,000 per annum Annual bonus Potential for overtime for out of core hours working/TOIL Pension Flexible benefits (access to our benefits platform for discounts and cash back on shopping purchases, gyms and leisure activities, cycle to work scheme and dedicated wellbeing centre)?
About Us: Invinity Energy Systems (LON: IES) Invinity Energy Systems is the leading global manufacturer of modular vanadium flow batteries for utility-scale energy storage deployments that unlock low-cost, low-carbon renewable energy on demand for businesses, industry, and electricity networks around the world. Safe, reliable, durable, and economical, Invinity's flow batteries are the most commercially proven alternative to lithium-ion and help to accelerate global progress towards Net Zero. We havecommercial projects in Europe, North America, Asia, and Australia, with office locations in Vancouver, BC, and Bathgate, Scotland, London, UK, and San Francisco, California. Job Description Reporting to the Manager, Materials R&D, the Principal Research Scientist is an experienced Electrochemist first and foremost with broad and deep experience in vanadium flow battery electro-active materials R&D. You will work as a "hands-on" researcher within Invinity's experienced R&D team while also providing expert science and analytical skills, training, mentorship and domain knowledge to the broader R&D team that is rapidly advance Invinity's next generation commercial products. Throughout your career, you will have demonstrated an excellent track record of delivering flow battery materials R&D that met or exceeded targets, including all lifecycle aspects from idea conception, and R&D program execution in multi-discipline teams, to a verified technology demonstrated at lab scale (Technology Readiness Level 1 through 5 inclusive). The successful candidate will be working independently in the lab, collaboratively with external R&D partners, and have a broad knowledge of state-of-the-art flow battery science and adjacent scientific fields required for battery R&D. Qualifications Responsibilities: Plan and conduct electrochemical R&D of next-generation materials and flow battery devices. Identify, investigate, and assess pre-production R&D material and analytical techniques for the advancement of flow battery science. Refine and develop new electrochemical test methods. Train and teach electrochemical first-principals theory, including the development of 1st principal's mathematical models for the prediction of electrochemical performance and degradation mechanisms. Collaborate with cross-functional R&D, Engineering, and Manufacturing teams to provide expert electro-chemical theory and practical skills in the development of Invinity next-generation technologies. Domain knowledge creation and awareness skills; understand state-of-the-art flow battery science in literature and patents for the creation of new patent applications. Knowledge, Experience, and Skills Required: A PhD degree in Electrochemistry or PhD in related fields with demonstrated equivalent electrochemistry experience. 10+ years of demonstrated expertise and growth in flow battery electrochemical R&D for commercial products. 15+ years' experience with electrochemical materials R&D. Proven ability to set and achieve clear research targets at the forefront of flow battery science. Demonstrated ability and desire to excel in a project-based, deliverables-driven R&D environment. Proven ability to effectively communicate in writing: research reports, published technical papers, patent applications, etc. Demonstrated interpersonal and verbal communication skills; must be able to communicate complex science to a wide range of stakeholders. Team player with the independence of thought and opinion to provide candor and honesty when making critical business decisions. Expert data analytical, task prioritization, and organizational skills. All other flow battery skills and experience are considered assets, please highlight in your application. (e.g. batter accelerated life testing R&D, electrolyte formulation and processing, cell materials formulation and synthesis, etc.) Travel Requirements: Up to 10% travel may be required for this position Additional Information If you believe that successful companies have at their foundation great science that is aligned with company strategy, if you want to be part of a committed and capable team, and if you are an expert at what you do, Invinity may be the place for you. Let's talk!
Apr 30, 2024
Full time
About Us: Invinity Energy Systems (LON: IES) Invinity Energy Systems is the leading global manufacturer of modular vanadium flow batteries for utility-scale energy storage deployments that unlock low-cost, low-carbon renewable energy on demand for businesses, industry, and electricity networks around the world. Safe, reliable, durable, and economical, Invinity's flow batteries are the most commercially proven alternative to lithium-ion and help to accelerate global progress towards Net Zero. We havecommercial projects in Europe, North America, Asia, and Australia, with office locations in Vancouver, BC, and Bathgate, Scotland, London, UK, and San Francisco, California. Job Description Reporting to the Manager, Materials R&D, the Principal Research Scientist is an experienced Electrochemist first and foremost with broad and deep experience in vanadium flow battery electro-active materials R&D. You will work as a "hands-on" researcher within Invinity's experienced R&D team while also providing expert science and analytical skills, training, mentorship and domain knowledge to the broader R&D team that is rapidly advance Invinity's next generation commercial products. Throughout your career, you will have demonstrated an excellent track record of delivering flow battery materials R&D that met or exceeded targets, including all lifecycle aspects from idea conception, and R&D program execution in multi-discipline teams, to a verified technology demonstrated at lab scale (Technology Readiness Level 1 through 5 inclusive). The successful candidate will be working independently in the lab, collaboratively with external R&D partners, and have a broad knowledge of state-of-the-art flow battery science and adjacent scientific fields required for battery R&D. Qualifications Responsibilities: Plan and conduct electrochemical R&D of next-generation materials and flow battery devices. Identify, investigate, and assess pre-production R&D material and analytical techniques for the advancement of flow battery science. Refine and develop new electrochemical test methods. Train and teach electrochemical first-principals theory, including the development of 1st principal's mathematical models for the prediction of electrochemical performance and degradation mechanisms. Collaborate with cross-functional R&D, Engineering, and Manufacturing teams to provide expert electro-chemical theory and practical skills in the development of Invinity next-generation technologies. Domain knowledge creation and awareness skills; understand state-of-the-art flow battery science in literature and patents for the creation of new patent applications. Knowledge, Experience, and Skills Required: A PhD degree in Electrochemistry or PhD in related fields with demonstrated equivalent electrochemistry experience. 10+ years of demonstrated expertise and growth in flow battery electrochemical R&D for commercial products. 15+ years' experience with electrochemical materials R&D. Proven ability to set and achieve clear research targets at the forefront of flow battery science. Demonstrated ability and desire to excel in a project-based, deliverables-driven R&D environment. Proven ability to effectively communicate in writing: research reports, published technical papers, patent applications, etc. Demonstrated interpersonal and verbal communication skills; must be able to communicate complex science to a wide range of stakeholders. Team player with the independence of thought and opinion to provide candor and honesty when making critical business decisions. Expert data analytical, task prioritization, and organizational skills. All other flow battery skills and experience are considered assets, please highlight in your application. (e.g. batter accelerated life testing R&D, electrolyte formulation and processing, cell materials formulation and synthesis, etc.) Travel Requirements: Up to 10% travel may be required for this position Additional Information If you believe that successful companies have at their foundation great science that is aligned with company strategy, if you want to be part of a committed and capable team, and if you are an expert at what you do, Invinity may be the place for you. Let's talk!
Regulatory Affairs Biocides Associate Manager Location: Frimley Surrey Function: GSARA (global safety assessment and regulatory affairs) Here at SC Johnson Ltd , we have an opportunity for a Regulatory Affairs Biocides Associate Manager to join our teambased in Frimley . You will join us on a full-time, permanent basisin return for a competitive salary, profit share and many more benefits SC Johnson is a fifth-generation family company built on a spirit of adventure and winning the right way. We have been leading with purpose for over 130 years, building top brands such as Raid , Glade , Kiwi , OFF! , Windex , Ziploc and more, in virtually every country. Through these household names, we are making a positive difference to the world around us. But we only succeed with the combined vitality and strength of our 13,000 people who we truly value and support in their pursuit of individual and shared goals. About the Regulatory Affairs Biocides Associate Manager role: The Global Registration and Regulatory Compliance (GRRC) team provide regulatory leadership, expertise and execution for the information/dossier development, product registration and lifecycle management of all SC Johnson products. In this role you will assist in the co-ordination and execution of regional compliance activities for SCJ Pest Control (PC) products in the European region associated with key pieces of EU legislation including, but not limited to BPR , CLP and REACH. In particular, coordinate GSARA's input into various EU Pest Control projects, determining dossier requirements and helping secure National Scheme and BPR (Biocidal Products Regulation) product registrations. Involvement in projects in other business groups may also be required on occasion. Key responsibilities of our Regulatory Affairs Biocides Associate Manager: You will interact with the GRRC team as appropriate to ensure the timely translation and adoption of relevant regulatory policy into company processes with alignment to regional regulatory strategy. For example key responsibilities within the PC category include: Regulatory : Support the GRRC team to provide product-specific requirements based on detailed knowledge of relevant EU regulations to ensure all new products (NPD) are fully compliant with regulations. Ensure any new regulations / interpretations are understood and communicated to stakeholders Maintenance of existing products in light of growing Safety, Regulatory & Environmental issues and constraints: Changes / additions to legislation are taken account for the EU PC product portfolios Project / Pre-launch: Project team participation: Input into project timelines and success criteria and attend relevant project meetings Input to project resource needs: Help determine the level of GSARA resource required for projects and feed information back to the functional leaders Post Launch : Ensure alignment and appropriate escalation to GSARA Management Committee of any critical issues Work with the Global Registration and Regulatory Compliance (GRRC) team to provide regulatory support for products in Market Previous experience / knowledge required of our Regulatory Affairs Biocides Associate Manager: BSc or MSc degree (or equivalent) preferably in a related Science field (Chemistry, Biology etc) is strongly preferred Good working experience with either BPR or PPR Regulations Demonstrated ability to work with different cultures Strong knowledge of compliance requirements across EU region Competencies, behaviors and aptitudes required of our Regulatory Affairs Biocides Associate Manager: Demonstrated communication skills, must be able to summarise and articulate technical information to diverse audiences both verbally and in writing Problem solving skills with the ability to bring projects to a conclusion Self-directed with a "can do" attitude and willingness to drive change What we can offer our Regulatory Affairs Biocides Associate Manager: Flexible starting and finishing times + 4.5 day working week Profit Share, Pension, Life cover & Health Insurance Shuttle bus service from local train stations, EV Charging points, Cycle to Work Scheme Free onsite Gym with free classes If you feel you have what it takes to become our Regulatory Affairs Biocides Associate Manager , then please click 'apply' now!
Apr 29, 2024
Full time
Regulatory Affairs Biocides Associate Manager Location: Frimley Surrey Function: GSARA (global safety assessment and regulatory affairs) Here at SC Johnson Ltd , we have an opportunity for a Regulatory Affairs Biocides Associate Manager to join our teambased in Frimley . You will join us on a full-time, permanent basisin return for a competitive salary, profit share and many more benefits SC Johnson is a fifth-generation family company built on a spirit of adventure and winning the right way. We have been leading with purpose for over 130 years, building top brands such as Raid , Glade , Kiwi , OFF! , Windex , Ziploc and more, in virtually every country. Through these household names, we are making a positive difference to the world around us. But we only succeed with the combined vitality and strength of our 13,000 people who we truly value and support in their pursuit of individual and shared goals. About the Regulatory Affairs Biocides Associate Manager role: The Global Registration and Regulatory Compliance (GRRC) team provide regulatory leadership, expertise and execution for the information/dossier development, product registration and lifecycle management of all SC Johnson products. In this role you will assist in the co-ordination and execution of regional compliance activities for SCJ Pest Control (PC) products in the European region associated with key pieces of EU legislation including, but not limited to BPR , CLP and REACH. In particular, coordinate GSARA's input into various EU Pest Control projects, determining dossier requirements and helping secure National Scheme and BPR (Biocidal Products Regulation) product registrations. Involvement in projects in other business groups may also be required on occasion. Key responsibilities of our Regulatory Affairs Biocides Associate Manager: You will interact with the GRRC team as appropriate to ensure the timely translation and adoption of relevant regulatory policy into company processes with alignment to regional regulatory strategy. For example key responsibilities within the PC category include: Regulatory : Support the GRRC team to provide product-specific requirements based on detailed knowledge of relevant EU regulations to ensure all new products (NPD) are fully compliant with regulations. Ensure any new regulations / interpretations are understood and communicated to stakeholders Maintenance of existing products in light of growing Safety, Regulatory & Environmental issues and constraints: Changes / additions to legislation are taken account for the EU PC product portfolios Project / Pre-launch: Project team participation: Input into project timelines and success criteria and attend relevant project meetings Input to project resource needs: Help determine the level of GSARA resource required for projects and feed information back to the functional leaders Post Launch : Ensure alignment and appropriate escalation to GSARA Management Committee of any critical issues Work with the Global Registration and Regulatory Compliance (GRRC) team to provide regulatory support for products in Market Previous experience / knowledge required of our Regulatory Affairs Biocides Associate Manager: BSc or MSc degree (or equivalent) preferably in a related Science field (Chemistry, Biology etc) is strongly preferred Good working experience with either BPR or PPR Regulations Demonstrated ability to work with different cultures Strong knowledge of compliance requirements across EU region Competencies, behaviors and aptitudes required of our Regulatory Affairs Biocides Associate Manager: Demonstrated communication skills, must be able to summarise and articulate technical information to diverse audiences both verbally and in writing Problem solving skills with the ability to bring projects to a conclusion Self-directed with a "can do" attitude and willingness to drive change What we can offer our Regulatory Affairs Biocides Associate Manager: Flexible starting and finishing times + 4.5 day working week Profit Share, Pension, Life cover & Health Insurance Shuttle bus service from local train stations, EV Charging points, Cycle to Work Scheme Free onsite Gym with free classes If you feel you have what it takes to become our Regulatory Affairs Biocides Associate Manager , then please click 'apply' now!
Are you an experienced Medicinal Chemist looking for a new opportunity? Maybe you are looking for an office-based role, where you can transfer your knowledge and skills from the laboratory? A Drug Discovery company are looking for a Chemistry Project Manager to join their team! They combine subject matter experts with drug development chemists to provide transformative programs based on breakthorugh discoveries. The role as Chemistry Project Manager will see you co-ordinate and screen activities across the company portfolio working closely with medicinal chemists, program directors and extenal partners. It will allow for someone with a great understanding of DMPK, Toxicology and preclinical drug discovery processes to facilitate assessment of synthetic routes design and target delivery at CROs. What does the role as Chemistry Project Manager involve? Liaising with program directors, medicinal chemists and external partners Facilitating assessments of synthetic route design and target delivery at CROs Ownership of chemistry and company database Operational management of screening cascades and compund logistics between networked CROs Patent writing and co-ordination of patent activities What experience is desired? A Medicinal or Synthetic Chemistry PhD or equivalent Experience in industry with a working technical knowledge of medicinal and synthetic chemistry Knowledge of DMPK and Toxicology characterisation of lead molecules Experience of route design, troubleshooting and data analysis for a wide range of modalities Critical review of proposals and published literature This role is based in the South East and is offered on a hybrid basis. If you would like to apply for the Chemistry Project Manager role, apply with your most up to date copy of your CV on word format (no more than 2 pages).
Apr 29, 2024
Full time
Are you an experienced Medicinal Chemist looking for a new opportunity? Maybe you are looking for an office-based role, where you can transfer your knowledge and skills from the laboratory? A Drug Discovery company are looking for a Chemistry Project Manager to join their team! They combine subject matter experts with drug development chemists to provide transformative programs based on breakthorugh discoveries. The role as Chemistry Project Manager will see you co-ordinate and screen activities across the company portfolio working closely with medicinal chemists, program directors and extenal partners. It will allow for someone with a great understanding of DMPK, Toxicology and preclinical drug discovery processes to facilitate assessment of synthetic routes design and target delivery at CROs. What does the role as Chemistry Project Manager involve? Liaising with program directors, medicinal chemists and external partners Facilitating assessments of synthetic route design and target delivery at CROs Ownership of chemistry and company database Operational management of screening cascades and compund logistics between networked CROs Patent writing and co-ordination of patent activities What experience is desired? A Medicinal or Synthetic Chemistry PhD or equivalent Experience in industry with a working technical knowledge of medicinal and synthetic chemistry Knowledge of DMPK and Toxicology characterisation of lead molecules Experience of route design, troubleshooting and data analysis for a wide range of modalities Critical review of proposals and published literature This role is based in the South East and is offered on a hybrid basis. If you would like to apply for the Chemistry Project Manager role, apply with your most up to date copy of your CV on word format (no more than 2 pages).
Geo-Environmental Consultant Brighton What it's like to work at Argyll: We're a friendly, dynamic and supportive team. We encourage passion, ambition and collaboration, both in our performance as a team and individually. New ideas are encouraged. We actively promote involvement in the development and direction of our products and services, as well as finding more efficient ways to work. We also love a good work social and team building events. As well as this we offer: 25 days' holiday, with optional 5 days unpaid leave per year Flexible working Free fruit, biscuits, tea and coffee, as well as cake on your birthday Annual lifestyle allowance of £300 to put towards an activity of your choice Cycle to Work scheme and Gym Flex scheme Private health insurance Internal coaching/mentoring system throughout your time here Focus on training and career progression Competitive salary The Opportunity The Consultant will primarily be involved in the delivery of in-house contaminated land consultancy services, as well managing projects including out-sourced services. A third of your time will be spent supporting with the daily report workload as well as supporting and training more junior staff with all aspects of our in-house services. You will be responsible for taking on complex consultancy projects including the full range of our consultancy services and bespoke portfolio projects. The role will involve: Reviewing Desktop Reports (all types) - 30% time spent Take responsibly for keeping up SLAs Reviewing desktop reports (all levels of complexity) Undertaking consultancy work - 40% time spent Writing/reviewing contaminated land consults Writing all levels of proposals for in-house contaminated land consultancy products as well as the full range of out-sourced services Assisting or project managing a business area Project management for large scale due diligence portfolios Undertaking and reviewing environmental audits (compliance and planning) Technical review of third party Phase II reports with supervision from Senior Consult level Other projects e.g. product development and training - 30% time spent Coaching Assistant Consultants Undertaking training presentations to new employees Leading CPDs to clients Networking to promote new business Account management Supports on technical aspects of new products/refresh of existing products About you As a Geo-Environmental Consultant, you will have experience of working within the sector mastering core skills such as completion of and quoting/scoping audits and associated services. You will have a strong commercial awareness and will develop and maintain relationships with key clients. You will also have/be: BA/BSc (Hons) in an Environmental Science or a similar discipline such as Biology, Chemistry, Geography, Geology or GIS. Working towards Associate member of the Institute of Environmental Management and Assessment (IEMA) and IEMA accredited Associate Environmental Auditor. Ability to write & review accurate desktop reports at all levels of complexity, complex regulatory consultation, standard in-house contaminated land consultancy products and standard proposals. Project & Supplier Management skills. Excellent written and oral communication skills. About Us Argyll Environmental are part of the Landmark Information Group, with bright, modern offices in Brighton city centre. Argyll are contaminated land and flood risk specialists. We deliver environmental insight to the majority of the top law firms in the UK, along with other niche markets such as SIPPs, asset managers, architects and developers. Landmark are leading environmental and property data experts, so together we are well placed to offer innovative products and services to the wider market. Our work is varied and could be anything from a small project to help someone gain planning permission, to supporting national scale property portfolios. Regardless of the project, we pride ourselves on offering an unrivalled level of service for our clients. We are proud to be an equal opportunities employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Apr 26, 2024
Full time
Geo-Environmental Consultant Brighton What it's like to work at Argyll: We're a friendly, dynamic and supportive team. We encourage passion, ambition and collaboration, both in our performance as a team and individually. New ideas are encouraged. We actively promote involvement in the development and direction of our products and services, as well as finding more efficient ways to work. We also love a good work social and team building events. As well as this we offer: 25 days' holiday, with optional 5 days unpaid leave per year Flexible working Free fruit, biscuits, tea and coffee, as well as cake on your birthday Annual lifestyle allowance of £300 to put towards an activity of your choice Cycle to Work scheme and Gym Flex scheme Private health insurance Internal coaching/mentoring system throughout your time here Focus on training and career progression Competitive salary The Opportunity The Consultant will primarily be involved in the delivery of in-house contaminated land consultancy services, as well managing projects including out-sourced services. A third of your time will be spent supporting with the daily report workload as well as supporting and training more junior staff with all aspects of our in-house services. You will be responsible for taking on complex consultancy projects including the full range of our consultancy services and bespoke portfolio projects. The role will involve: Reviewing Desktop Reports (all types) - 30% time spent Take responsibly for keeping up SLAs Reviewing desktop reports (all levels of complexity) Undertaking consultancy work - 40% time spent Writing/reviewing contaminated land consults Writing all levels of proposals for in-house contaminated land consultancy products as well as the full range of out-sourced services Assisting or project managing a business area Project management for large scale due diligence portfolios Undertaking and reviewing environmental audits (compliance and planning) Technical review of third party Phase II reports with supervision from Senior Consult level Other projects e.g. product development and training - 30% time spent Coaching Assistant Consultants Undertaking training presentations to new employees Leading CPDs to clients Networking to promote new business Account management Supports on technical aspects of new products/refresh of existing products About you As a Geo-Environmental Consultant, you will have experience of working within the sector mastering core skills such as completion of and quoting/scoping audits and associated services. You will have a strong commercial awareness and will develop and maintain relationships with key clients. You will also have/be: BA/BSc (Hons) in an Environmental Science or a similar discipline such as Biology, Chemistry, Geography, Geology or GIS. Working towards Associate member of the Institute of Environmental Management and Assessment (IEMA) and IEMA accredited Associate Environmental Auditor. Ability to write & review accurate desktop reports at all levels of complexity, complex regulatory consultation, standard in-house contaminated land consultancy products and standard proposals. Project & Supplier Management skills. Excellent written and oral communication skills. About Us Argyll Environmental are part of the Landmark Information Group, with bright, modern offices in Brighton city centre. Argyll are contaminated land and flood risk specialists. We deliver environmental insight to the majority of the top law firms in the UK, along with other niche markets such as SIPPs, asset managers, architects and developers. Landmark are leading environmental and property data experts, so together we are well placed to offer innovative products and services to the wider market. Our work is varied and could be anything from a small project to help someone gain planning permission, to supporting national scale property portfolios. Regardless of the project, we pride ourselves on offering an unrivalled level of service for our clients. We are proud to be an equal opportunities employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Job Description Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It Matter. As an organization we are committed to developing the next generation of Makers and Bakers. Joining us at an early career stage in our fast paced and ever changing environment will enable you to do more, learn more and grow more. You will be encouraged to step outside your comfort zone- you may even surprise yourself! We will ensure you are given the support you need to be at your best and enable you to be yourself and bring passion and personality. Here you can lean in and speak up and bring your own flavor. Big enough to reach the top. Small enough to help you get off the ground. Are you studying towards an Engineering or Science Degree' (e.g. food science, nutrition, engineering or related discipline) Do you want a taste of the career you could have with Mondelez? Sink your teeth into one of our sweet internships. Our Internships are 12 months long (although some roles have the flexibility to be shorter) and during your placement, we'll make you an integral part of our team and give you a real job - with real responsibilities - from day one. We hope to help you expand your horizons and encourage your personal and professional development. We want to make sure you get the most from your time with us. That's why once you join we'll work out ambitious but achievable goals for you. Then through the support of a mentor and regular reviews with your manager, we'll help you achieve them. Life in Research Development Quality (R&D): As an intern at Mondelēz International you will be responsible and accountable for your project(s). During the placement you will be expected to plan and execute tests of various scale (e.g. benchtop, pilot plant, and factory) as appropriate for your project as well as to coordinate informal sensory assessment. Key deliverables would be to produce technical reports/presentations and periodically communicate your key findings to stakeholders. You will also have the opportunity to interact with the wider R&D Community, other business functions and external suppliers. In addition to this you may also be expected to support other ongoing project activities in and outside of your immediate team. For some roles, occasional international travel may be required. This job description is relating to roles in our Bournville Chocolate Research and Development location. Technology Discovery: The technology discovery team unlocks future technology to enable the business to grow, by understanding how science and technology advances can be applied creatively to our products. You will be surrounded by world class experts in cocoa, chocolate, fats and confectionery science and engineering. Disciplines: Food Science and all Engineering disciplines, e.g. chemical, mechanical and food. Essential Candidate requirements Studying towards a Food Science, Engineering or other scientific discipline (e.g. Chemistry, Biology, Biochemistry, Food & Nutrition, Physical Sciences, Materials Science, Physics) 2:1 degree - predicted end result (or equivalent) Self-drive and motivation Naturally inquisitive and passionate about technical excellence and sciences and can apply fundamental knowledge practically Can work with a level of autonomy, as well as works well in a team Demonstrates strong analytical, communication and presentation abilities Pro-active, highly motivated, ready to take on new responsibilities and build strong relationships Organisation and planning skills If there are opportunities, able to travel overseas, for plant trials/commissioning work and occasionally work on shift, as projects needs dictate Good working knowledge of MS Office We recruit throughout the year and we review our applications on a first come, first served basis. We also reserve the right to close our vacancies early and therefore we recommend that you complete and submit your application as soon as possible. Mondelēz is a diverse and inclusive employer with an objective to ensure a fair and equal hiring process. If you require any reasonable adjustments to apply or throughout our assessment process please contact stating "NE Early Careers" as the subject. Our candidate requirements are based on criteria to enable you to succeed in the role. If you have narrowly missed the above requirements and there are extenuating circumstances that you would like us to consider, you can let us know by contacting stating "NE Early Careers" as the subject and attaching a letter from your school/university to confirm your extenuating circumstances. The responsibilities of this position are performed within the framework of a regional business model that is defined and managed by Mondelēz Europe GmbH, Switzerland . Business Unit Summary At Mondelez Europe, we are proud, not only of the iconic brands we make, but also of the people who make them. Our delicious products are created in 52 plants across Europe by more than 28,000 passionate people. We are the top maker of chocolate and biscuits and a leading maker of gum and candy. We make sure our powerful global brands and local jewels like Cadbury , Milka and Alpen Gold chocolates, Oreo , belVita , LU and Tuc biscuits, and Stimorol and Dirol gums get safely into our customers hands-and mouths. Great people and great brands. That's who we are. Join us on our journey to continue leading the future of snacking around the world by offering the right snack, for the right moment, made the right way. Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type Intern (Fixed Term) Interns Early Careers
Sep 23, 2022
Full time
Job Description Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It Matter. As an organization we are committed to developing the next generation of Makers and Bakers. Joining us at an early career stage in our fast paced and ever changing environment will enable you to do more, learn more and grow more. You will be encouraged to step outside your comfort zone- you may even surprise yourself! We will ensure you are given the support you need to be at your best and enable you to be yourself and bring passion and personality. Here you can lean in and speak up and bring your own flavor. Big enough to reach the top. Small enough to help you get off the ground. Are you studying towards an Engineering or Science Degree' (e.g. food science, nutrition, engineering or related discipline) Do you want a taste of the career you could have with Mondelez? Sink your teeth into one of our sweet internships. Our Internships are 12 months long (although some roles have the flexibility to be shorter) and during your placement, we'll make you an integral part of our team and give you a real job - with real responsibilities - from day one. We hope to help you expand your horizons and encourage your personal and professional development. We want to make sure you get the most from your time with us. That's why once you join we'll work out ambitious but achievable goals for you. Then through the support of a mentor and regular reviews with your manager, we'll help you achieve them. Life in Research Development Quality (R&D): As an intern at Mondelēz International you will be responsible and accountable for your project(s). During the placement you will be expected to plan and execute tests of various scale (e.g. benchtop, pilot plant, and factory) as appropriate for your project as well as to coordinate informal sensory assessment. Key deliverables would be to produce technical reports/presentations and periodically communicate your key findings to stakeholders. You will also have the opportunity to interact with the wider R&D Community, other business functions and external suppliers. In addition to this you may also be expected to support other ongoing project activities in and outside of your immediate team. For some roles, occasional international travel may be required. This job description is relating to roles in our Bournville Chocolate Research and Development location. Technology Discovery: The technology discovery team unlocks future technology to enable the business to grow, by understanding how science and technology advances can be applied creatively to our products. You will be surrounded by world class experts in cocoa, chocolate, fats and confectionery science and engineering. Disciplines: Food Science and all Engineering disciplines, e.g. chemical, mechanical and food. Essential Candidate requirements Studying towards a Food Science, Engineering or other scientific discipline (e.g. Chemistry, Biology, Biochemistry, Food & Nutrition, Physical Sciences, Materials Science, Physics) 2:1 degree - predicted end result (or equivalent) Self-drive and motivation Naturally inquisitive and passionate about technical excellence and sciences and can apply fundamental knowledge practically Can work with a level of autonomy, as well as works well in a team Demonstrates strong analytical, communication and presentation abilities Pro-active, highly motivated, ready to take on new responsibilities and build strong relationships Organisation and planning skills If there are opportunities, able to travel overseas, for plant trials/commissioning work and occasionally work on shift, as projects needs dictate Good working knowledge of MS Office We recruit throughout the year and we review our applications on a first come, first served basis. We also reserve the right to close our vacancies early and therefore we recommend that you complete and submit your application as soon as possible. Mondelēz is a diverse and inclusive employer with an objective to ensure a fair and equal hiring process. If you require any reasonable adjustments to apply or throughout our assessment process please contact stating "NE Early Careers" as the subject. Our candidate requirements are based on criteria to enable you to succeed in the role. If you have narrowly missed the above requirements and there are extenuating circumstances that you would like us to consider, you can let us know by contacting stating "NE Early Careers" as the subject and attaching a letter from your school/university to confirm your extenuating circumstances. The responsibilities of this position are performed within the framework of a regional business model that is defined and managed by Mondelēz Europe GmbH, Switzerland . Business Unit Summary At Mondelez Europe, we are proud, not only of the iconic brands we make, but also of the people who make them. Our delicious products are created in 52 plants across Europe by more than 28,000 passionate people. We are the top maker of chocolate and biscuits and a leading maker of gum and candy. We make sure our powerful global brands and local jewels like Cadbury , Milka and Alpen Gold chocolates, Oreo , belVita , LU and Tuc biscuits, and Stimorol and Dirol gums get safely into our customers hands-and mouths. Great people and great brands. That's who we are. Join us on our journey to continue leading the future of snacking around the world by offering the right snack, for the right moment, made the right way. Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type Intern (Fixed Term) Interns Early Careers
Job Description Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It With Pride. Working as part of a cross functional team, you deliver the RDQ activities required to complete new product development, portfolio maintenance and/or productivity projects with an emphasis on meeting the desired consumer experience. How you will contribute With the support and guidance of a manager, you will organize and execute projects in line with RDQ, marketing and manufacturing requirements, effectively communicating status and risks. You will plan and conduct pilot plant and factory trials in accordance with good manufacturing practice and HACCP requirements and development activities (e.g. product shelf-life testing, designing for quality, consumer test preparation etc.). You will also write technical reports that will require the analysis and interpretation of results and that lead to conclusions and recommendations and create and maintain accurate consumer-led specifications. What you will bring A desire to drive your future and accelerate your career and the following experience and knowledge: Food science, science, or engineering ideally in a fast-moving consumer goods market Working on teams and independently with the guidance of a manager Prioritizing and managing activities Identifying problems proactively and creating and implementing solutions independently Applying fundamental technical understanding to interpret and analyze data to reach clear conclusions Communicating effectively verbally and in writing, including technical writing Putting the consumer at the heart of development activities More about this role What you need to know about this position: Ernest Jackson & Co Ltd exists to deliver the best tasting healthcare products to consumers. Unique to Mondelez international, Ernest Jackson has a locally managed Research and Development function whose goal is to: Develop the right healthcare products to meet the needs of the consumer and enable a competitive edge for the business. As a member of the R&D department this role develops new; food, nutraceutical and pharmaceutical products for predominantly UK markets but also international export. You will develop recipes, specifications, standards and manufacturing procedures for new products. Creating protocols for safe and effective trialing and testing, and producing reports that justify the efficacy of our products for release to market. This will all be completed in accordance with GMP, HACCP, ICH, MHRA, FDA, FSSC and health & safety guidelines and regulations. The Research and Development Department performs a wide range of projects in support of Ernest Jackson Business Objectives. Therefore, as well as product development, the development scientist is also expected to support process upgrades and production efficiencies. In this role you will support other business functions in ensuring any changes to process consider and mitigate the impact to product. This will include supporting and running trials, validation work, process design and supporting the creation of process parameters. You will be expected to work in an organised manner within tight deadlines to ensure that projects are delivered within expected time scales. The role holder will have or develop a working knowledge of both licenced medicine regulations and the nutritional landscape in order to design and develop new products that meet market and regulatory needs. The successful individual will be required to conduct project work on a wide range of projects, from development of new functional food (nutraceutical) products (most likely supporting another scientist), reviewing and controlling raw material changes, collating and reviewing product data used to justify characteristics including but not limited to analytical data of vitamins and minerals and organoleptic data of finished products. The successful individual would need to be able to work flexibly from site, we'd aim to retain at least a Mdlz 50:50 time split between home and office. The individual will need to supervise trials on site, support changes, conduct testing and taste panels on site. Looking for a candidate that can start as soon as possible The successful candidate would most likely be involved in our sustainability goals, investigating the impact of recyclable materials on our products and their shelf life What extra ingredients you will bring: Strong communication skills to sell ideas and solutions to senior stakeholders Inquisitive; the successful candidate will support with root cause investigations, looking for someone who will keep digging, keep investigating and ruling things out, good at crunching data. Process orientated; R&D support the business in maintaining robust GMP processes Data driven; goes without saying we crunch data and solve a lot of issues that require evidence Other stuff The successful individual will have exposure to pharmaceutical products and pharmaceutical development but unlikely to lead on any pharmaceutical projects, might be a selling point Potentially open to individuals with Engineering background instead of food development/Chemistry/science background if they're the right fit Education / Certifications: Must BSc in Chemistry, life science, or other scientific discipline Proficient in MS Office applications especially Word, Excel, and PowerPoint Fluent in English (written and spoken communication) Preferred Experience in product development Some experience in the FMCG sector Experience in a lab environment (we don't develop in one, but some skills are transferable) Experience in project-based work/development Knowledge in Food product law/technical aspects of food development Job specific requirements: Must Be able to work in an agile manor, capable of working on multiple tracks of work/objectives at once Be inquisitive, want to learn and develop their understanding, willing to ask questions and reasons Strong interpersonal skills, good influencing ability Passion Understand timelines/deadlines Good ability to plan and organise own work, prioritising where necessary Integrity/honesty/trust Attention to detail Process orientated: won't struggle with prescriptive processes or being bound by pharmaceutical regulations Preferred Confident presenting ideas Strong stakeholder management and persuasion skills Good commercial awareness Analytical thought process: able to define ways to test and prove concepts, a rigorous scientific approach Financial understanding of costs/impacts/benefits Work schedule: This is a maternity cover fixed term contract. This role offers hybrid working. The responsibilities of this position are performed within the framework of a regional business model that is defined and managed by Mondelēz Europe GmbH, Switzerland . No Relocation support available Business Unit Summary At Mondelez Europe, we are proud, not only of the iconic brands we make, but also of the people who make them. Our delicious products are created in 52 plants across Europe by more than 28,000 passionate people. We are the top maker of chocolate and biscuits and a leading maker of gum and candy. We make sure our powerful global brands and local jewels like Cadbury , Milka and Alpen Gold chocolates, Oreo , belVita , LU and Tuc biscuits, and Stimorol and Dirol gums get safely into our customers hands-and mouths. Great people and great brands. That's who we are. Join us on our journey to continue leading the future of snacking around the world by offering the right snack, for the right moment, made the right way. Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type Temporary (Fixed Term) Product development Science & Engineering
Sep 23, 2022
Full time
Job Description Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It With Pride. Working as part of a cross functional team, you deliver the RDQ activities required to complete new product development, portfolio maintenance and/or productivity projects with an emphasis on meeting the desired consumer experience. How you will contribute With the support and guidance of a manager, you will organize and execute projects in line with RDQ, marketing and manufacturing requirements, effectively communicating status and risks. You will plan and conduct pilot plant and factory trials in accordance with good manufacturing practice and HACCP requirements and development activities (e.g. product shelf-life testing, designing for quality, consumer test preparation etc.). You will also write technical reports that will require the analysis and interpretation of results and that lead to conclusions and recommendations and create and maintain accurate consumer-led specifications. What you will bring A desire to drive your future and accelerate your career and the following experience and knowledge: Food science, science, or engineering ideally in a fast-moving consumer goods market Working on teams and independently with the guidance of a manager Prioritizing and managing activities Identifying problems proactively and creating and implementing solutions independently Applying fundamental technical understanding to interpret and analyze data to reach clear conclusions Communicating effectively verbally and in writing, including technical writing Putting the consumer at the heart of development activities More about this role What you need to know about this position: Ernest Jackson & Co Ltd exists to deliver the best tasting healthcare products to consumers. Unique to Mondelez international, Ernest Jackson has a locally managed Research and Development function whose goal is to: Develop the right healthcare products to meet the needs of the consumer and enable a competitive edge for the business. As a member of the R&D department this role develops new; food, nutraceutical and pharmaceutical products for predominantly UK markets but also international export. You will develop recipes, specifications, standards and manufacturing procedures for new products. Creating protocols for safe and effective trialing and testing, and producing reports that justify the efficacy of our products for release to market. This will all be completed in accordance with GMP, HACCP, ICH, MHRA, FDA, FSSC and health & safety guidelines and regulations. The Research and Development Department performs a wide range of projects in support of Ernest Jackson Business Objectives. Therefore, as well as product development, the development scientist is also expected to support process upgrades and production efficiencies. In this role you will support other business functions in ensuring any changes to process consider and mitigate the impact to product. This will include supporting and running trials, validation work, process design and supporting the creation of process parameters. You will be expected to work in an organised manner within tight deadlines to ensure that projects are delivered within expected time scales. The role holder will have or develop a working knowledge of both licenced medicine regulations and the nutritional landscape in order to design and develop new products that meet market and regulatory needs. The successful individual will be required to conduct project work on a wide range of projects, from development of new functional food (nutraceutical) products (most likely supporting another scientist), reviewing and controlling raw material changes, collating and reviewing product data used to justify characteristics including but not limited to analytical data of vitamins and minerals and organoleptic data of finished products. The successful individual would need to be able to work flexibly from site, we'd aim to retain at least a Mdlz 50:50 time split between home and office. The individual will need to supervise trials on site, support changes, conduct testing and taste panels on site. Looking for a candidate that can start as soon as possible The successful candidate would most likely be involved in our sustainability goals, investigating the impact of recyclable materials on our products and their shelf life What extra ingredients you will bring: Strong communication skills to sell ideas and solutions to senior stakeholders Inquisitive; the successful candidate will support with root cause investigations, looking for someone who will keep digging, keep investigating and ruling things out, good at crunching data. Process orientated; R&D support the business in maintaining robust GMP processes Data driven; goes without saying we crunch data and solve a lot of issues that require evidence Other stuff The successful individual will have exposure to pharmaceutical products and pharmaceutical development but unlikely to lead on any pharmaceutical projects, might be a selling point Potentially open to individuals with Engineering background instead of food development/Chemistry/science background if they're the right fit Education / Certifications: Must BSc in Chemistry, life science, or other scientific discipline Proficient in MS Office applications especially Word, Excel, and PowerPoint Fluent in English (written and spoken communication) Preferred Experience in product development Some experience in the FMCG sector Experience in a lab environment (we don't develop in one, but some skills are transferable) Experience in project-based work/development Knowledge in Food product law/technical aspects of food development Job specific requirements: Must Be able to work in an agile manor, capable of working on multiple tracks of work/objectives at once Be inquisitive, want to learn and develop their understanding, willing to ask questions and reasons Strong interpersonal skills, good influencing ability Passion Understand timelines/deadlines Good ability to plan and organise own work, prioritising where necessary Integrity/honesty/trust Attention to detail Process orientated: won't struggle with prescriptive processes or being bound by pharmaceutical regulations Preferred Confident presenting ideas Strong stakeholder management and persuasion skills Good commercial awareness Analytical thought process: able to define ways to test and prove concepts, a rigorous scientific approach Financial understanding of costs/impacts/benefits Work schedule: This is a maternity cover fixed term contract. This role offers hybrid working. The responsibilities of this position are performed within the framework of a regional business model that is defined and managed by Mondelēz Europe GmbH, Switzerland . No Relocation support available Business Unit Summary At Mondelez Europe, we are proud, not only of the iconic brands we make, but also of the people who make them. Our delicious products are created in 52 plants across Europe by more than 28,000 passionate people. We are the top maker of chocolate and biscuits and a leading maker of gum and candy. We make sure our powerful global brands and local jewels like Cadbury , Milka and Alpen Gold chocolates, Oreo , belVita , LU and Tuc biscuits, and Stimorol and Dirol gums get safely into our customers hands-and mouths. Great people and great brands. That's who we are. Join us on our journey to continue leading the future of snacking around the world by offering the right snack, for the right moment, made the right way. Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type Temporary (Fixed Term) Product development Science & Engineering
Divisional Plant & Fleet Manager (VN2993) Business Area: Fleet, Plant & Workshops Vacancy Base: Eurovia Roadstone, Dangenham County: Essex Contract Type: Permanent Hours: 40 Ringway is a market leader in the Highways Term Maintenance Industry, responsible for looking after over 50,000 kms of the UK's highways network. We take pride in offering a dedicated, flexible approach which supports our clients, underpinned by the recruitment, development and retention of a locally based workforce. We want you to grow your career in a way that suits you, whether that is making the best of your skills in a role you enjoy, or developing new skills as you progress with our company. Activities of the team/department that this role will operate in; Production of Asphalt, modified bitumen and bitumen emulsion manufacture. Purpose of the role and your responsibilities; Member of the Production leadership team focused on the management of Maintenance, Engineering and Capital Expenditure projects to support commercial, customer services, safety, and operational personnel. No direct reports, but will need to manage and supervise external contractors. Formal qualifications required; 5-10 years experience in a similar role Mechanical engineering qualification ideal but not essential Skills required; -Effective communication -Excellent Time Management -PC literacy -Organisational skills -Accuracy/attention to detail -Ability to work with minimal supervision -Demonstrated initiative -Ability to work to deadlines Experience required; -Steady work record with proven interest in the management of maintenance and projects. -Previous hands on experience with heavy machinery/process equipment -Previous experience working with asphalt plants, process plants, quarying ideal, but not essential Knowledge; A good understanding of Chemistry, Physics and Mathematics. Personal qualities; -Previous good attendance -Driven to achieve performance targets -Efficient mindset Awarded Investors in People Silver, a member of the 5% Club and recognised as an Investor in Diversity. Providing opportunity and growth for all our employees is the bedrock of our business, ensuring a safe, happy and productive workforce. We have a dedicated recruitment team and politely request that agencies refrain from contacting anyone across our businesses with regards to speculative CV's or offering to assist with our vacancies, thank you. Ringway recognises the importance of helping our employees balance their work and home life by offering flexible working arrangements across many of our roles.
Sep 23, 2022
Full time
Divisional Plant & Fleet Manager (VN2993) Business Area: Fleet, Plant & Workshops Vacancy Base: Eurovia Roadstone, Dangenham County: Essex Contract Type: Permanent Hours: 40 Ringway is a market leader in the Highways Term Maintenance Industry, responsible for looking after over 50,000 kms of the UK's highways network. We take pride in offering a dedicated, flexible approach which supports our clients, underpinned by the recruitment, development and retention of a locally based workforce. We want you to grow your career in a way that suits you, whether that is making the best of your skills in a role you enjoy, or developing new skills as you progress with our company. Activities of the team/department that this role will operate in; Production of Asphalt, modified bitumen and bitumen emulsion manufacture. Purpose of the role and your responsibilities; Member of the Production leadership team focused on the management of Maintenance, Engineering and Capital Expenditure projects to support commercial, customer services, safety, and operational personnel. No direct reports, but will need to manage and supervise external contractors. Formal qualifications required; 5-10 years experience in a similar role Mechanical engineering qualification ideal but not essential Skills required; -Effective communication -Excellent Time Management -PC literacy -Organisational skills -Accuracy/attention to detail -Ability to work with minimal supervision -Demonstrated initiative -Ability to work to deadlines Experience required; -Steady work record with proven interest in the management of maintenance and projects. -Previous hands on experience with heavy machinery/process equipment -Previous experience working with asphalt plants, process plants, quarying ideal, but not essential Knowledge; A good understanding of Chemistry, Physics and Mathematics. Personal qualities; -Previous good attendance -Driven to achieve performance targets -Efficient mindset Awarded Investors in People Silver, a member of the 5% Club and recognised as an Investor in Diversity. Providing opportunity and growth for all our employees is the bedrock of our business, ensuring a safe, happy and productive workforce. We have a dedicated recruitment team and politely request that agencies refrain from contacting anyone across our businesses with regards to speculative CV's or offering to assist with our vacancies, thank you. Ringway recognises the importance of helping our employees balance their work and home life by offering flexible working arrangements across many of our roles.
Scientist Up to £45,000 DOE Hemel Hempstead A new and exciting opportunity has arisen with our client based in Hemel Hempstead, to join a team of experience scientist, who are at the forefront of innovation for the UK security market. As part of the Products & Technology Department, you will be working as part of a team of knowledgeable and motivated scientists, technology experts and project leaders, driving product development and support for all future innovation. This is a permanent role, offering site based flexible working as and when possible. You will provide scientific expertise and support, ranging from instrument/experimental design, data analysis and modelling, to the formulation of conclusions and report writing. Duties & Responsibilities Provide scientific support and guidance to the design, build and testing of experimental security equipment. Conduct original research for design and performance enhancement of products. Critically appraise experimental data and theory and provide guidance based on interpretation of data. Support scientific aspects of products throughout their lifecycle. Provide hands-on support and up-to-date technical advice to Technical Authorities, Product and Programme Managers, at proposal, design specification, development, testing and production stages while assisting in bid preparation. Ideal candidate must have: Master's degree in chemistry or physics - essential (PhD preferred) Experience of analytical instrument design with a solid understanding of how the apparatus works - essential Knowledge of ion mobility spectrometry - highly advantageous. Experimental scientist with excellent data analysis skills - highly advantageous High level of innovation and original research, R&D experience - desirable Please contact for more information or to register your interest At Morgan Ryder we can provide you with a full range of employment opportunities from short term and fixed term temporary vacancies to permanent positions. We recruit for companies that operate in the following industries: Food and Drink Manufacturers, FMCG, Packaging, Engineering, Automotive, Aerospace, Warehousing, Logistics, Waste Management, Petro Chemical, Pharmaceutical, Power & Renewable Energy. Please note that calls to and from the offices of Morgan Ryder Associates Ltd. may be monitored or recorded. This is to ensure compliance with regulatory procedures, record business transactions and for training purposes.
Sep 21, 2022
Full time
Scientist Up to £45,000 DOE Hemel Hempstead A new and exciting opportunity has arisen with our client based in Hemel Hempstead, to join a team of experience scientist, who are at the forefront of innovation for the UK security market. As part of the Products & Technology Department, you will be working as part of a team of knowledgeable and motivated scientists, technology experts and project leaders, driving product development and support for all future innovation. This is a permanent role, offering site based flexible working as and when possible. You will provide scientific expertise and support, ranging from instrument/experimental design, data analysis and modelling, to the formulation of conclusions and report writing. Duties & Responsibilities Provide scientific support and guidance to the design, build and testing of experimental security equipment. Conduct original research for design and performance enhancement of products. Critically appraise experimental data and theory and provide guidance based on interpretation of data. Support scientific aspects of products throughout their lifecycle. Provide hands-on support and up-to-date technical advice to Technical Authorities, Product and Programme Managers, at proposal, design specification, development, testing and production stages while assisting in bid preparation. Ideal candidate must have: Master's degree in chemistry or physics - essential (PhD preferred) Experience of analytical instrument design with a solid understanding of how the apparatus works - essential Knowledge of ion mobility spectrometry - highly advantageous. Experimental scientist with excellent data analysis skills - highly advantageous High level of innovation and original research, R&D experience - desirable Please contact for more information or to register your interest At Morgan Ryder we can provide you with a full range of employment opportunities from short term and fixed term temporary vacancies to permanent positions. We recruit for companies that operate in the following industries: Food and Drink Manufacturers, FMCG, Packaging, Engineering, Automotive, Aerospace, Warehousing, Logistics, Waste Management, Petro Chemical, Pharmaceutical, Power & Renewable Energy. Please note that calls to and from the offices of Morgan Ryder Associates Ltd. may be monitored or recorded. This is to ensure compliance with regulatory procedures, record business transactions and for training purposes.
Proclinical is excited to partner with an international drug discovery and development company in Cambridge to find a Project Manager to join their Research and Development group. THE ROLE The successful candidate will play a key role in the management of multiple drug discovery programmes from early research through to development and early clinical phases. Working within multi-disciplinary teams they will be responsible for the delivery of projects to defined plans, timelines and costs. In a fast-moving environment, they will need to be highly organised with outstanding attention to detail, have a pro-active approach to challenges and demonstrate exceptional team-working skills. Main Responsibilities • Input into the preparation of project plans, budgets and contractual agreements. • Contribute to scientific and operational discussions with clients and functional experts to define project strategy and goals. • Manage in-house and outsourced project activities to deliver projects to agreed plans. • Act as key point of contact for clients, collaborators and contract research organisations. • Administer internal and external team meetings ensuring responsibilities are defined and stakeholders work to agreed plans. • Drive high-performance of project teams, ensuring clear communication and effective decision making. • Manage scientific documentation and data for project progression, patent filing, regulatory submissions and in preparation for asset or corporate sale. • Contribute to the development of internal operational systems to support company growth. Skills/Requirements • Postgraduate degree in a life science (Biology, Chemistry or similar_ • Ideally three years' experience gained within a pharmaceutical or biotechnology company preferably in a project management role. • Exceptional interpersonal, communication and presentation skills. • Strong time management and organisational skills to enable planning of work on multiple projects during daily routine. • Experience of working in a matrix organisation with multi-disciplinary teams. • Ability to resolve conflicts at different levels of the organisation to facilitate a positive outcome. • Familiarity with standard Project Management tools and processes
Feb 24, 2022
Full time
Proclinical is excited to partner with an international drug discovery and development company in Cambridge to find a Project Manager to join their Research and Development group. THE ROLE The successful candidate will play a key role in the management of multiple drug discovery programmes from early research through to development and early clinical phases. Working within multi-disciplinary teams they will be responsible for the delivery of projects to defined plans, timelines and costs. In a fast-moving environment, they will need to be highly organised with outstanding attention to detail, have a pro-active approach to challenges and demonstrate exceptional team-working skills. Main Responsibilities • Input into the preparation of project plans, budgets and contractual agreements. • Contribute to scientific and operational discussions with clients and functional experts to define project strategy and goals. • Manage in-house and outsourced project activities to deliver projects to agreed plans. • Act as key point of contact for clients, collaborators and contract research organisations. • Administer internal and external team meetings ensuring responsibilities are defined and stakeholders work to agreed plans. • Drive high-performance of project teams, ensuring clear communication and effective decision making. • Manage scientific documentation and data for project progression, patent filing, regulatory submissions and in preparation for asset or corporate sale. • Contribute to the development of internal operational systems to support company growth. Skills/Requirements • Postgraduate degree in a life science (Biology, Chemistry or similar_ • Ideally three years' experience gained within a pharmaceutical or biotechnology company preferably in a project management role. • Exceptional interpersonal, communication and presentation skills. • Strong time management and organisational skills to enable planning of work on multiple projects during daily routine. • Experience of working in a matrix organisation with multi-disciplinary teams. • Ability to resolve conflicts at different levels of the organisation to facilitate a positive outcome. • Familiarity with standard Project Management tools and processes
Regulatory Affairs Manager £60k salary + Bonus + Benefits Based - Richmond, Surrey,TW9 Mon - Fri 9am - 5.30pm Immediate start Candidate must have experience with UK, Ireland and EU Pharmaceutical legislation. Role: To manage the Regulatory Affairs team to sustain continuous market supply and patient safety, providing expertise and knowledge of regulatory environment to support the Consilient Health business strategy.Ensure products manufactured on behalf of Company and marketed comply with EU legislation. Degree in a suitable scientific discipline (biological/chemistry/life sciences) Knowledge and appreciation of ABPI/IPHA Codes of Practice relevant to responsibilities. In depth knowledge of local and European regulatory affairs/PV legislation and guidance Substantial regulatory experience across the full product lifecycle Broad experience of managing relevant regulatory submissions, with demonstrated ability to work independently and manage complex projects Ability to assess the business impact of new legislation and guidance Deep understanding of quality aspects of the business and the impact of regulatory activities. Experience of managing a team Planning and organisation skills- ability to multitask A confident credible communicator Excellent written communication skills with attention to detail. Able to build relationships at all levels Analytical with strong decision making skills, able to apply judgement Benefits: Paid Holidays - 25 days per annum. UK bank holidays are additional to your annual leave entitlement. Flexibility Policy in place - There will be flexibility to allow you to work from home on an agreed day or days. Laptop/Computer & Mobile Phone - for use in relation to company business. Access to the Bupa Employment Assistance Program from day one of employment. Specsavers Eyecare Scheme. The Probation Period will be 6 months. A Notice Period 3 months. Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.
Feb 24, 2022
Full time
Regulatory Affairs Manager £60k salary + Bonus + Benefits Based - Richmond, Surrey,TW9 Mon - Fri 9am - 5.30pm Immediate start Candidate must have experience with UK, Ireland and EU Pharmaceutical legislation. Role: To manage the Regulatory Affairs team to sustain continuous market supply and patient safety, providing expertise and knowledge of regulatory environment to support the Consilient Health business strategy.Ensure products manufactured on behalf of Company and marketed comply with EU legislation. Degree in a suitable scientific discipline (biological/chemistry/life sciences) Knowledge and appreciation of ABPI/IPHA Codes of Practice relevant to responsibilities. In depth knowledge of local and European regulatory affairs/PV legislation and guidance Substantial regulatory experience across the full product lifecycle Broad experience of managing relevant regulatory submissions, with demonstrated ability to work independently and manage complex projects Ability to assess the business impact of new legislation and guidance Deep understanding of quality aspects of the business and the impact of regulatory activities. Experience of managing a team Planning and organisation skills- ability to multitask A confident credible communicator Excellent written communication skills with attention to detail. Able to build relationships at all levels Analytical with strong decision making skills, able to apply judgement Benefits: Paid Holidays - 25 days per annum. UK bank holidays are additional to your annual leave entitlement. Flexibility Policy in place - There will be flexibility to allow you to work from home on an agreed day or days. Laptop/Computer & Mobile Phone - for use in relation to company business. Access to the Bupa Employment Assistance Program from day one of employment. Specsavers Eyecare Scheme. The Probation Period will be 6 months. A Notice Period 3 months. Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.