Job Title: Principal Chemical Analyst Location: Cambridge (Lab Based) Job type: 24-Months Fixed Term Contract At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees. Working within the Analytical Services section of the Quality Department laboratories a Senior Analyst will provide high quality scientific and analytical expertise for a variety of pharmaceutical dosage forms. Execute activities related to process and /or product improvement activities. Ensure manufacturing departments are supported in their day to day operations with relevant deviation and process improvement oversight. Seek out improvement opportunities and make suggestions to management for changes in practice and technical innovation. Act as an Analytical expert on a wide range of projects. Will be expected to develop supervisory skills by undertaking more responsibility for the day to day operation of the laboratory. Role and responsibilities Lead the execution of analytical method transfers between laboratories. Support and help to develop analytical validation strategies, ensuring all aspects of analytical development and validation are delivered to the required standard of science, quality and regulatory compliance in accordance with agreed timelines. Assist with and ensure Quality Management System processes such as Change Controls, Deviations, CAPAs and Quality Risk management procedures are undertaken and progressed as required. Lead Analytical investigations. Plan, coordinate and conduct laboratory work to support analytical projects, this can be including analysis of raw materials, intermediates and finished products. Record, evaluate and present data generated during laboratory work both internally and by third parties, by applying expert scientific knowledge, demonstrating a practical approach and providing appropriate and innovative solutions. Be proficient and proactive in the use of regulatory and other relevant guidelines, including pharmacopoeias, to ensure appropriate compliance within projects. Provide appropriate and consolidated CMC or pharmaceutical analysis opinion to ensure successful project outcomes. What you'll bring Minimum 5 years of years of experience in pharmaceutical testing laboratories. Experience with HPLCs is essential. Experience with Dissolution, APIs, tablets, and capsules forms are desirable. Proven track record in analytical chemistry and or analytical development for drug product formulations as well as experience in CMC/regulatory guidelines and filings Significant industrial experience working in or maintaining a GMP/GLP compliant analytical environment. Experience with EU regulatory guidelines, quality management systems and quality risk assessments. What we offer in return flexible benefits package opportunities for learning & development collaborative, inclusive work environment Diversity and inclusion Building an inclusive environment where people can thrive, grow and achieve their full potential is a priority. We believe this isn't just the right thing, but also the smart thing to do, as we focus on making a positive difference for our customers and their patients. About Mundipharma Mundipharma is a global healthcare company with a presence across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East. Mundipharma is dedicated to bringing innovative treatments to patients in the areas of Pain Management, Infectious Disease and Consumer Healthcare as well as other severe debilitating disease areas. Our guiding principles, centered around Integrity and Patients-Centricity, are at the heart of everything we do. Join our talent pool If you're not sure this role is right for you but you're keen to hear about future opportunities at Mundipharma, join our talent community and be the first to hear about new roles. Additional Job Description: Primary Location: GB Cambridge Job Posting Date: 2024-04-07 Job Type: Fixed Term Contract (Fixed Term)
May 03, 2024
Full time
Job Title: Principal Chemical Analyst Location: Cambridge (Lab Based) Job type: 24-Months Fixed Term Contract At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees. Working within the Analytical Services section of the Quality Department laboratories a Senior Analyst will provide high quality scientific and analytical expertise for a variety of pharmaceutical dosage forms. Execute activities related to process and /or product improvement activities. Ensure manufacturing departments are supported in their day to day operations with relevant deviation and process improvement oversight. Seek out improvement opportunities and make suggestions to management for changes in practice and technical innovation. Act as an Analytical expert on a wide range of projects. Will be expected to develop supervisory skills by undertaking more responsibility for the day to day operation of the laboratory. Role and responsibilities Lead the execution of analytical method transfers between laboratories. Support and help to develop analytical validation strategies, ensuring all aspects of analytical development and validation are delivered to the required standard of science, quality and regulatory compliance in accordance with agreed timelines. Assist with and ensure Quality Management System processes such as Change Controls, Deviations, CAPAs and Quality Risk management procedures are undertaken and progressed as required. Lead Analytical investigations. Plan, coordinate and conduct laboratory work to support analytical projects, this can be including analysis of raw materials, intermediates and finished products. Record, evaluate and present data generated during laboratory work both internally and by third parties, by applying expert scientific knowledge, demonstrating a practical approach and providing appropriate and innovative solutions. Be proficient and proactive in the use of regulatory and other relevant guidelines, including pharmacopoeias, to ensure appropriate compliance within projects. Provide appropriate and consolidated CMC or pharmaceutical analysis opinion to ensure successful project outcomes. What you'll bring Minimum 5 years of years of experience in pharmaceutical testing laboratories. Experience with HPLCs is essential. Experience with Dissolution, APIs, tablets, and capsules forms are desirable. Proven track record in analytical chemistry and or analytical development for drug product formulations as well as experience in CMC/regulatory guidelines and filings Significant industrial experience working in or maintaining a GMP/GLP compliant analytical environment. Experience with EU regulatory guidelines, quality management systems and quality risk assessments. What we offer in return flexible benefits package opportunities for learning & development collaborative, inclusive work environment Diversity and inclusion Building an inclusive environment where people can thrive, grow and achieve their full potential is a priority. We believe this isn't just the right thing, but also the smart thing to do, as we focus on making a positive difference for our customers and their patients. About Mundipharma Mundipharma is a global healthcare company with a presence across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East. Mundipharma is dedicated to bringing innovative treatments to patients in the areas of Pain Management, Infectious Disease and Consumer Healthcare as well as other severe debilitating disease areas. Our guiding principles, centered around Integrity and Patients-Centricity, are at the heart of everything we do. Join our talent pool If you're not sure this role is right for you but you're keen to hear about future opportunities at Mundipharma, join our talent community and be the first to hear about new roles. Additional Job Description: Primary Location: GB Cambridge Job Posting Date: 2024-04-07 Job Type: Fixed Term Contract (Fixed Term)
At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees. Working within the Analytical Services section of the Quality Department laboratories a Senior Analyst will provide high quality scientific and analytical expertise for a variety of pharmaceutical dosage forms. Execute activities related to process and /or product improvement activities. Ensure manufacturing departments are supported in their day to day operations with relevant deviation and process improvement oversight. Seek out improvement opportunities and make suggestions to management for changes in practice and technical innovation. Act as an Analytical expert on a wide range of projects. Will be expected to develop supervisory skills by undertaking more responsibility for the day to day operation of the laboratory. Role and responsibilities Lead the execution of analytical method transfers between laboratories. Support and help to develop analytical validation strategies, ensuring all aspects of analytical development and validation are delivered to the required standard of science, quality and regulatory compliance in accordance with agreed timelines. Assist with and ensure Quality Management System processes such as Change Controls, Deviations, CAPAs and Quality Risk management procedures are undertaken and progressed as required. Lead Analytical investigations. Plan, coordinate and conduct laboratory work to support analytical projects, this can be including analysis of raw materials, intermediates and finished products. Record, evaluate and present data generated during laboratory work both internally and by third parties, by applying expert scientific knowledge, demonstrating a practical approach and providing appropriate and innovative solutions. Be proficient and proactive in the use of regulatory and other relevant guidelines, including pharmacopoeias, to ensure appropriate compliance within projects. Provide appropriate and consolidated CMC or pharmaceutical analysis opinion to ensure successful project outcomes. What you'll bring Minimum 5 years of years of experience in pharmaceutical testing laboratories. Experience with HPLCs is essential. Experience with Dissolution, APIs, tablets, and capsules forms are desirable. Proven track record in analytical chemistry and or analytical development for drug product formulations as well as experience in CMC/regulatory guidelines and filings Significant industrial experience working in or maintaining a GMP/GLP compliant analytical environment. Experience with EU regulatory guidelines, quality management systems and quality risk assessments. What we offer in return flexible benefits package opportunities for learning & development collaborative, inclusive work environment
May 01, 2024
Full time
At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees. Working within the Analytical Services section of the Quality Department laboratories a Senior Analyst will provide high quality scientific and analytical expertise for a variety of pharmaceutical dosage forms. Execute activities related to process and /or product improvement activities. Ensure manufacturing departments are supported in their day to day operations with relevant deviation and process improvement oversight. Seek out improvement opportunities and make suggestions to management for changes in practice and technical innovation. Act as an Analytical expert on a wide range of projects. Will be expected to develop supervisory skills by undertaking more responsibility for the day to day operation of the laboratory. Role and responsibilities Lead the execution of analytical method transfers between laboratories. Support and help to develop analytical validation strategies, ensuring all aspects of analytical development and validation are delivered to the required standard of science, quality and regulatory compliance in accordance with agreed timelines. Assist with and ensure Quality Management System processes such as Change Controls, Deviations, CAPAs and Quality Risk management procedures are undertaken and progressed as required. Lead Analytical investigations. Plan, coordinate and conduct laboratory work to support analytical projects, this can be including analysis of raw materials, intermediates and finished products. Record, evaluate and present data generated during laboratory work both internally and by third parties, by applying expert scientific knowledge, demonstrating a practical approach and providing appropriate and innovative solutions. Be proficient and proactive in the use of regulatory and other relevant guidelines, including pharmacopoeias, to ensure appropriate compliance within projects. Provide appropriate and consolidated CMC or pharmaceutical analysis opinion to ensure successful project outcomes. What you'll bring Minimum 5 years of years of experience in pharmaceutical testing laboratories. Experience with HPLCs is essential. Experience with Dissolution, APIs, tablets, and capsules forms are desirable. Proven track record in analytical chemistry and or analytical development for drug product formulations as well as experience in CMC/regulatory guidelines and filings Significant industrial experience working in or maintaining a GMP/GLP compliant analytical environment. Experience with EU regulatory guidelines, quality management systems and quality risk assessments. What we offer in return flexible benefits package opportunities for learning & development collaborative, inclusive work environment
Customs Process Analyst - 37704 Pay Rate: up to £25.78/hr Ltd inside IR35 (c. £19.75/hr PAYE option) Division: Finance Initial 3 month contract position based at Whitley / hybrid working Position Description: This role sits with the Global Finance Services - Customs Process Team and will support the day-to-day transactional Customs declarations needed for import and exports through both manual and automated processes. This is a data input and workflow supervisory role and requires no previous Customs experience. Key Accountabilities and Responsibilities Support the preparation of Customs Declarations in accordance with defined processes Assist with the review of backing documentation to ensure compliance with appropriate tax law e.g., check of validity of invoices, calculations on backing spreadsheet, and highlighting points of concern to more senior staff Monitor the performance of small teams based at an India shared service centre (2-3 FTE) Provide manual assistance to automated solutions Carry out all work with a high degree of accuracy Follow a script of FAQs to support enquiries Undertake any other work as directed by their line manager in connection with their job as may be requested Daily communication with India based shared service team, external logistics providers, customs brokers and internal stakeholders Essential Skills, Knowledge and Experience: Ability to effectively interpret and communicate base data and input into systems Good analytical skills with an attention to detail Excel skills Excellent telephone manner Good communication skills Experience Preferred: Experience of GTS module of SAP Some knowledge of Customs formalities Personal Profile: An individual with the ability to prioritise their own and the team's workload A good communicator An effective team player and leader who supports team members Ability to delegate and ensure tasks are completed in an agile manner Resilient and enthusiastic, an individual able to deliver results under pressure Ability to see the wider picture and prioritise workloads Additional Information: ** THIS POSITION IS CONFIRMED INSIDE IR35 ** For further information, please send your interest and CV to Your CV will be forwarded to Jonathan Lee Recruitment, a leading engineering and manufacturing recruitment consultancy established in 1978. The services advertised by Jonathan Lee Contracts are those of an Employment Business.
Feb 26, 2022
Contractor
Customs Process Analyst - 37704 Pay Rate: up to £25.78/hr Ltd inside IR35 (c. £19.75/hr PAYE option) Division: Finance Initial 3 month contract position based at Whitley / hybrid working Position Description: This role sits with the Global Finance Services - Customs Process Team and will support the day-to-day transactional Customs declarations needed for import and exports through both manual and automated processes. This is a data input and workflow supervisory role and requires no previous Customs experience. Key Accountabilities and Responsibilities Support the preparation of Customs Declarations in accordance with defined processes Assist with the review of backing documentation to ensure compliance with appropriate tax law e.g., check of validity of invoices, calculations on backing spreadsheet, and highlighting points of concern to more senior staff Monitor the performance of small teams based at an India shared service centre (2-3 FTE) Provide manual assistance to automated solutions Carry out all work with a high degree of accuracy Follow a script of FAQs to support enquiries Undertake any other work as directed by their line manager in connection with their job as may be requested Daily communication with India based shared service team, external logistics providers, customs brokers and internal stakeholders Essential Skills, Knowledge and Experience: Ability to effectively interpret and communicate base data and input into systems Good analytical skills with an attention to detail Excel skills Excellent telephone manner Good communication skills Experience Preferred: Experience of GTS module of SAP Some knowledge of Customs formalities Personal Profile: An individual with the ability to prioritise their own and the team's workload A good communicator An effective team player and leader who supports team members Ability to delegate and ensure tasks are completed in an agile manner Resilient and enthusiastic, an individual able to deliver results under pressure Ability to see the wider picture and prioritise workloads Additional Information: ** THIS POSITION IS CONFIRMED INSIDE IR35 ** For further information, please send your interest and CV to Your CV will be forwarded to Jonathan Lee Recruitment, a leading engineering and manufacturing recruitment consultancy established in 1978. The services advertised by Jonathan Lee Contracts are those of an Employment Business.
Do you want to work for Luxury Automotive OEM? We have a number of contract opportunities for Customs Process Analyst working for Luxury Automotive OEM based in Coventry, West Midlands Position Description: This role sits with the Global Finance Services - Customs process team The role is to support the day-to-day transactional Customs declarations needed for import and exports through both manual and automated processes. This is a data input and workflow supervisory role and requires no previous Customs experience. Key Accountabilities and Responsibilities: Support the preparation of Customs Declarations in accordance with defined processes Assist with the review of backing documentation to ensure compliance with appropriate tax law e.g. check of validity of invoices, calculations on backing spreadsheet, and highlighting points of concern to more senior staff Monitor the performance of small teams based at an India shared service centre (2-3 FTE) Provide manual assistance to automated solutions Carry out all work with a high degree of accuracy. Follow a script of FAQs to support enquiries Undertake any other work as directed by their line manager in connection with their job as may be requested Daily communication with India based shared service team, external logistics providers, customs brokers and internal JLR stakeholders Knowledge, Skills and Experience Essential: Ability to effectively interpret and communicate base data and input into JLR systems Good analytical skills with an attention to detail Excel skills Good Telephone manner Good Communication skills Experience Preferred: Desirable: Experience of GTS module of SAP Some knowledge of Customs formalities Key Performance Indicators: To answer questions on all aspects of Customs Processes Support Customs Analysts and team leaders with timely query resolution Communicate via email and telephone Recognise complex Customs issues and escalate Quality and volume metrics on customs clearances. Personal Profile Essential: An individual with the ability to prioritise theirs and the team's workload A good communicator An effective team player and leader who supports team members Ability to delegate and ensure tasks are completed in an agile manner Resilient and enthusiastic, an individual able to deliver results under pressure Ability to see the wider picture and prioritise workloads If you want to know more about this NEW contract role please APPLY today.... We will process your CV and personal information to assess your suitability for the role. If we wish to consider you further, we will register your personal information in our database and contact you. We may contact you from time to time about other relevant roles. Your personal information will be securely held. For more information please refer to our privacy notice, a copy of which can be found on our website. - Select Engineering Limited.
Feb 23, 2022
Contractor
Do you want to work for Luxury Automotive OEM? We have a number of contract opportunities for Customs Process Analyst working for Luxury Automotive OEM based in Coventry, West Midlands Position Description: This role sits with the Global Finance Services - Customs process team The role is to support the day-to-day transactional Customs declarations needed for import and exports through both manual and automated processes. This is a data input and workflow supervisory role and requires no previous Customs experience. Key Accountabilities and Responsibilities: Support the preparation of Customs Declarations in accordance with defined processes Assist with the review of backing documentation to ensure compliance with appropriate tax law e.g. check of validity of invoices, calculations on backing spreadsheet, and highlighting points of concern to more senior staff Monitor the performance of small teams based at an India shared service centre (2-3 FTE) Provide manual assistance to automated solutions Carry out all work with a high degree of accuracy. Follow a script of FAQs to support enquiries Undertake any other work as directed by their line manager in connection with their job as may be requested Daily communication with India based shared service team, external logistics providers, customs brokers and internal JLR stakeholders Knowledge, Skills and Experience Essential: Ability to effectively interpret and communicate base data and input into JLR systems Good analytical skills with an attention to detail Excel skills Good Telephone manner Good Communication skills Experience Preferred: Desirable: Experience of GTS module of SAP Some knowledge of Customs formalities Key Performance Indicators: To answer questions on all aspects of Customs Processes Support Customs Analysts and team leaders with timely query resolution Communicate via email and telephone Recognise complex Customs issues and escalate Quality and volume metrics on customs clearances. Personal Profile Essential: An individual with the ability to prioritise theirs and the team's workload A good communicator An effective team player and leader who supports team members Ability to delegate and ensure tasks are completed in an agile manner Resilient and enthusiastic, an individual able to deliver results under pressure Ability to see the wider picture and prioritise workloads If you want to know more about this NEW contract role please APPLY today.... We will process your CV and personal information to assess your suitability for the role. If we wish to consider you further, we will register your personal information in our database and contact you. We may contact you from time to time about other relevant roles. Your personal information will be securely held. For more information please refer to our privacy notice, a copy of which can be found on our website. - Select Engineering Limited.
Job Title: Custom Process Analyst Location: Whitley, Coventry Rate: £ 25.27 ph via an Umbrella Company (Inside IR35) or £19.15 ph PAYE Employment Type: Contract (3 months) Hours: Standard 40 Hours Per Week Reference: J37704 Job Description: An individual with the ability to prioritise theirs and the teams workload. A good communicator. An effective team player and leader who supports team members. Ability to delegate and ensure tasks are completed in an agile manner resilient and enthusiastic, an individual able to deliver results under pressure. Ability to see the wider picture and prioritise workloads. Customs process analyst. This role sits with the global finance services - customs process team. The role is to support the day to day transactional customs declarations needed for import and exports through both manual and automated processes. This is a data input and workflow supervisory role and requires no previous customs experience. Skills Preferred: Support the preparation of customs declarations in accordance with defined processes. Assist with the review of backing documentation to ensure compliance with appropriate tax law e.g. check of validity of invoices, calculations on backing spreadsheet, and highlighting points of concern to more senior staff. Monitor the performance of small teams based at an India shared service centre (2-3 FTE). Provide manual assistance to automated solutions. Carry out all work with a high degree of accuracy. Follow a script of FAQs to support enquiries. Undertake any other work as directed by their line manager in connection with their job as may be requested. Daily communication with India based shared service team, external logistics providers, customs brokers and internal client stakeholders. To answer questions on all aspects of customs processes. Support customs analysts and team leaders with timely query resolution. Communicate via email and telephone. Recognise complex customs issues and escalate quality and volume metrics on customs clearances. Experience Required: Ability to effectively interpret and communicate base data and input into client systems. Good analytical skills with an attention to detail. Excel skills. Good telephone manner. Good communication skills. Experience Preferred: Experience of GTS module of SAP. Some knowledge of Customs formalities. Additional Information: This role is INSIDE IR35 Do not miss out on your chance of interview - APPLY NOW! Our Clients are unable to provide sponsorship for Tier 2 General Visas; therefore, only candidates eligible to work in the UK need apply! Caresoft Global Limited operates as an Employment Business and Employment Agency. We are an independent highly-experienced recruitment consultancy dedicated to specialist markets within the Automotive, Aerospace, Agricultural & Construction Industries. No terminology within this advert is intended to unlawfully discriminate on the grounds of age, sex, race or disability and we welcome all applications.
Feb 23, 2022
Contractor
Job Title: Custom Process Analyst Location: Whitley, Coventry Rate: £ 25.27 ph via an Umbrella Company (Inside IR35) or £19.15 ph PAYE Employment Type: Contract (3 months) Hours: Standard 40 Hours Per Week Reference: J37704 Job Description: An individual with the ability to prioritise theirs and the teams workload. A good communicator. An effective team player and leader who supports team members. Ability to delegate and ensure tasks are completed in an agile manner resilient and enthusiastic, an individual able to deliver results under pressure. Ability to see the wider picture and prioritise workloads. Customs process analyst. This role sits with the global finance services - customs process team. The role is to support the day to day transactional customs declarations needed for import and exports through both manual and automated processes. This is a data input and workflow supervisory role and requires no previous customs experience. Skills Preferred: Support the preparation of customs declarations in accordance with defined processes. Assist with the review of backing documentation to ensure compliance with appropriate tax law e.g. check of validity of invoices, calculations on backing spreadsheet, and highlighting points of concern to more senior staff. Monitor the performance of small teams based at an India shared service centre (2-3 FTE). Provide manual assistance to automated solutions. Carry out all work with a high degree of accuracy. Follow a script of FAQs to support enquiries. Undertake any other work as directed by their line manager in connection with their job as may be requested. Daily communication with India based shared service team, external logistics providers, customs brokers and internal client stakeholders. To answer questions on all aspects of customs processes. Support customs analysts and team leaders with timely query resolution. Communicate via email and telephone. Recognise complex customs issues and escalate quality and volume metrics on customs clearances. Experience Required: Ability to effectively interpret and communicate base data and input into client systems. Good analytical skills with an attention to detail. Excel skills. Good telephone manner. Good communication skills. Experience Preferred: Experience of GTS module of SAP. Some knowledge of Customs formalities. Additional Information: This role is INSIDE IR35 Do not miss out on your chance of interview - APPLY NOW! Our Clients are unable to provide sponsorship for Tier 2 General Visas; therefore, only candidates eligible to work in the UK need apply! Caresoft Global Limited operates as an Employment Business and Employment Agency. We are an independent highly-experienced recruitment consultancy dedicated to specialist markets within the Automotive, Aerospace, Agricultural & Construction Industries. No terminology within this advert is intended to unlawfully discriminate on the grounds of age, sex, race or disability and we welcome all applications.