We are partnered with a globally recognised leader in Human-Machine Interface technology who are seeking a Senior Embedded Software Engineer . Based in Nottinghamshire, with roots dating back to the 1940s and a long-standing reputation for innovation, this company designs and manufactures devices demanding applications including medical, marine, defence, aerospace, industrial, and air traffic control. As part of a respected international group, they maintain high-quality standards and export the products worldwide. This is an opportunity to join their market-leading R&D team and lead the design, development, and implementation of embedded software and firmware for cutting-edge electronic HMI products. Key Responsibilities for this Senior Embedded Software Engineer: Lead end-to-end software development: specification, design, implementation, testing, and documentation. Engineer firmware for embedded systems, including peripheral configuration and fault analysis. Architect layered software solutions for embedded portability. Work with protocols such as SPI, I C, I S, UART, USB, CAN, and Ethernet. Prepare technical specifications, test reports, and contribute to IP/innovation initiatives. Support production engineering-trialling and troubleshooting new developments. Provide technical leadership and mentorship to senior engineers and cross-functional colleagues. Support proposals with technical estimates, timelines, and cost information. Manage firmware lifecycle and change controls. Assist in new process creation and technical risk management. Qualifications & Experience Required for this Senior Embedded Software Engineer: BSc or MSc in Computer/Electronic Engineering, Computer Science, or related field. At least 6 years of hands-on embedded C development experience within electronics or manufacturing. Experience in additional programming languages (e.g C++) Familiarity with Microsoft Visual Audio Proficient with Git or similar version control systems. Demonstrated experience with bare-metal firmware development, layered architectures, and embedded testing (unit/automated). Exposure to task and issue tracking tools like Jira, and familiarity with IDE/toolchains and release management practices. Familiarity with Microsoft Visual Studio. Development of desktop utilities for product testing or customer interfaces. Strong analytical skills and ability to structure information for both internal and external audiences. Proficient in Microsoft Office suite (Excel, Word, PowerPoint, Outlook). Excellent initiative, communication, and adaptability. Salary & Benefits for this Senior Embedded Software Engineer role: Salary of up to 45,000 per annum. 25 days holiday plus bank holidays Regular Monday to Friday office hours Annual bonus Highstreet discounts Career progression
Sep 04, 2025
Full time
We are partnered with a globally recognised leader in Human-Machine Interface technology who are seeking a Senior Embedded Software Engineer . Based in Nottinghamshire, with roots dating back to the 1940s and a long-standing reputation for innovation, this company designs and manufactures devices demanding applications including medical, marine, defence, aerospace, industrial, and air traffic control. As part of a respected international group, they maintain high-quality standards and export the products worldwide. This is an opportunity to join their market-leading R&D team and lead the design, development, and implementation of embedded software and firmware for cutting-edge electronic HMI products. Key Responsibilities for this Senior Embedded Software Engineer: Lead end-to-end software development: specification, design, implementation, testing, and documentation. Engineer firmware for embedded systems, including peripheral configuration and fault analysis. Architect layered software solutions for embedded portability. Work with protocols such as SPI, I C, I S, UART, USB, CAN, and Ethernet. Prepare technical specifications, test reports, and contribute to IP/innovation initiatives. Support production engineering-trialling and troubleshooting new developments. Provide technical leadership and mentorship to senior engineers and cross-functional colleagues. Support proposals with technical estimates, timelines, and cost information. Manage firmware lifecycle and change controls. Assist in new process creation and technical risk management. Qualifications & Experience Required for this Senior Embedded Software Engineer: BSc or MSc in Computer/Electronic Engineering, Computer Science, or related field. At least 6 years of hands-on embedded C development experience within electronics or manufacturing. Experience in additional programming languages (e.g C++) Familiarity with Microsoft Visual Audio Proficient with Git or similar version control systems. Demonstrated experience with bare-metal firmware development, layered architectures, and embedded testing (unit/automated). Exposure to task and issue tracking tools like Jira, and familiarity with IDE/toolchains and release management practices. Familiarity with Microsoft Visual Studio. Development of desktop utilities for product testing or customer interfaces. Strong analytical skills and ability to structure information for both internal and external audiences. Proficient in Microsoft Office suite (Excel, Word, PowerPoint, Outlook). Excellent initiative, communication, and adaptability. Salary & Benefits for this Senior Embedded Software Engineer role: Salary of up to 45,000 per annum. 25 days holiday plus bank holidays Regular Monday to Friday office hours Annual bonus Highstreet discounts Career progression
If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma 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, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. The Senior Principal will be responsible for leading projects related to data engineering requirements and initiatives across Jazz Research and Development. The Senior Principal will lead data projects from across the business including Clinical, Pre-Clinical, Non-Clinical, Chemistry, RWD and Omics. Essential Functions Lead the design, development and maintenance of data pipelines for processing Research and Development data from diverse sources (Clinical Trials, Medical Devices, Pre-Clinical, Omics, Real World Data) utilizing the AWS technology platform. Create and optimize ETL/ELT processes for structured and unstructured data using Python, R, SQL, AWS services and other tools. Build and maintain data repositories using AWS S3 and FSx technologies. Establish data warehousing solutions using Amazon Redshift. Build and maintain standard data models. Own data quality frameworks, validation processes and KPIs to ensure accuracy and consistency of data pipelines. Implement data versioning and lineage tracking to support data traceability, regulatory compliance and audit requirements. Create and maintain documentation for data processes, architectures, and workflows. Implement modern software development best practices (e.g. Code Versioning, DevOps, CD/CI). Support collaboration with RnD Researchers, Data scientists and Stakeholders to understand data requirements and deliver appropriate solutions in a global working model. Maintain compliance with data privacy regulations such as HIPAA, GDPR May be required to develop, deliver or support data literacy training across R&D. Required Knowledge, Skills and Abilities Expert knowledge of data engineering tools such as Python, R and SQL for data processing. Expert proficiency with AWS services particularly S3, Redshift, FSx, Glue, Lambda. Expert proficiency with relational databases. Strong background in data modeling and database design. Strong knowledge with unstructured database technologies (e.g. NoSQL) and other database types (e.g. Graph). Experience with Containerization such as Docker and EKS/Kubernetes. Experience with one or more RnD research process and associated regulatory requirements. Exposure to healthcare data standards (CDISC, HL7, FHIR, SNOMED CT, OMOP, DICOM). Experience to big data technologies and handling. Knowledge of machine learning operations (MLOps) and model deployment. Strong problem-solving and analytical abilities. Excellent communication skills for collaborating with stakeholders. Experience working in an Agile development environment. Required/Preferred Education Bachelor's Degree in Computer Science, Statistics, Mathematics, Life Sciences, or other relevant scientific fields; Master's Degree preferred 5-7 years of experience in data engineering, with at least 2 years focusing on healthcare, research or clinical related data Description of Physical Demands Occasional mobility within office environment Routinely sitting for extended periods of time Constantly operating a computer, printer, telephone and other similar office machinery Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: .
Sep 04, 2025
Full time
If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma 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, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. The Senior Principal will be responsible for leading projects related to data engineering requirements and initiatives across Jazz Research and Development. The Senior Principal will lead data projects from across the business including Clinical, Pre-Clinical, Non-Clinical, Chemistry, RWD and Omics. Essential Functions Lead the design, development and maintenance of data pipelines for processing Research and Development data from diverse sources (Clinical Trials, Medical Devices, Pre-Clinical, Omics, Real World Data) utilizing the AWS technology platform. Create and optimize ETL/ELT processes for structured and unstructured data using Python, R, SQL, AWS services and other tools. Build and maintain data repositories using AWS S3 and FSx technologies. Establish data warehousing solutions using Amazon Redshift. Build and maintain standard data models. Own data quality frameworks, validation processes and KPIs to ensure accuracy and consistency of data pipelines. Implement data versioning and lineage tracking to support data traceability, regulatory compliance and audit requirements. Create and maintain documentation for data processes, architectures, and workflows. Implement modern software development best practices (e.g. Code Versioning, DevOps, CD/CI). Support collaboration with RnD Researchers, Data scientists and Stakeholders to understand data requirements and deliver appropriate solutions in a global working model. Maintain compliance with data privacy regulations such as HIPAA, GDPR May be required to develop, deliver or support data literacy training across R&D. Required Knowledge, Skills and Abilities Expert knowledge of data engineering tools such as Python, R and SQL for data processing. Expert proficiency with AWS services particularly S3, Redshift, FSx, Glue, Lambda. Expert proficiency with relational databases. Strong background in data modeling and database design. Strong knowledge with unstructured database technologies (e.g. NoSQL) and other database types (e.g. Graph). Experience with Containerization such as Docker and EKS/Kubernetes. Experience with one or more RnD research process and associated regulatory requirements. Exposure to healthcare data standards (CDISC, HL7, FHIR, SNOMED CT, OMOP, DICOM). Experience to big data technologies and handling. Knowledge of machine learning operations (MLOps) and model deployment. Strong problem-solving and analytical abilities. Excellent communication skills for collaborating with stakeholders. Experience working in an Agile development environment. Required/Preferred Education Bachelor's Degree in Computer Science, Statistics, Mathematics, Life Sciences, or other relevant scientific fields; Master's Degree preferred 5-7 years of experience in data engineering, with at least 2 years focusing on healthcare, research or clinical related data Description of Physical Demands Occasional mobility within office environment Routinely sitting for extended periods of time Constantly operating a computer, printer, telephone and other similar office machinery Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: .
Senior Embedded Software Engineer with strong skills in Embedded linux/Kernel development, Bootloader and device driver development, is required by a world-leading, high end customer centric device company to play a senior role in their new London tech hub based close to London Paddington, and join a Pan-European Embedded software engineering team of around 30 people. Salary: £80-103k + Decent Pension, Health, and 30 Days Holiday. The Embedded Software Engineer will take the lead in developing low-level Embedded systems, including the Linux Kernel, custom Embedded Linux distributions, bootloaders, device drivers, and board bring-up, among other tasks. While also having a significant impact on the entire physical product used by millions of customers, working as part of a cross-functional team. The Senior Embedded Software Engineer is a hybrid role and will ideally be based in the office 2/3 days per week. However, there might be some flexibility for those with outstanding Embedded Linux skills and strong Kernel development to work more remotely from within the UK. As a Senior Embedded Software Engineer, you will have skills in the majority of Strong expertise in Linux Kernel development, Kernel functions, and maintenance, with recent Kernel versions. Experience of working with physical Embedded products development/Devices/automotive/IOT with connectivity, etc Vast experience with Embedded C, Embedded systems and a solid understanding of Linux operating systems. Strong skills in developing device drivers, and driver implementation, as well as device trees. Experience with systemd or other init systems. Strong skills in Embedded bootloaders such as (Das) U-Boot, Grub, BarBox, preferably on ARM-based systems. Experience of planning, shaping of requirements specification, and development for both new and existing products. Proficiency in C++. Rust or another system programming language is ideal. Skilful at debugging and profiling complex Embedded Linux systems. Expert knowledge of hardware electronics, circuit diagrams, and experience with Yocto Project or Buildroot, Logic analysers etc The senior Embedded Software Engineer is responsible for two key areas: the first involves Embedded core activities, such as new hardware bring-up and maintenance (enabling new features to work). The other part can be diverse, including security, peripheral drivers, display, and power, which are highly relevant. While it encompasses the entire product, the focus is often on Linux bootloaders or device drivers. When security is involved, it pertains to the hardware, boot, or Linux components. This role would be ideal for an experienced Linux Engineer who has worked with physical products in areas such as automotive, medical devices, IOT, tablets, mobile devices, or consumer-centric physical devices. This is an outstanding opportunity to join a recently formed London-based team for a fast-growing and successful European scaleup company with amazing customer-centric products and a strong software engineering culture, excellent benefits, and a balanced approach to work-life balance. The role involves approximately two-thirds of trips a year within Europe to collaborate with the European engineering team, and great opportunities to progress with an ambitious product-centric business. Opus Resourcing acts as an employment agency with respect to permanent employment.
Sep 04, 2025
Seasonal
Senior Embedded Software Engineer with strong skills in Embedded linux/Kernel development, Bootloader and device driver development, is required by a world-leading, high end customer centric device company to play a senior role in their new London tech hub based close to London Paddington, and join a Pan-European Embedded software engineering team of around 30 people. Salary: £80-103k + Decent Pension, Health, and 30 Days Holiday. The Embedded Software Engineer will take the lead in developing low-level Embedded systems, including the Linux Kernel, custom Embedded Linux distributions, bootloaders, device drivers, and board bring-up, among other tasks. While also having a significant impact on the entire physical product used by millions of customers, working as part of a cross-functional team. The Senior Embedded Software Engineer is a hybrid role and will ideally be based in the office 2/3 days per week. However, there might be some flexibility for those with outstanding Embedded Linux skills and strong Kernel development to work more remotely from within the UK. As a Senior Embedded Software Engineer, you will have skills in the majority of Strong expertise in Linux Kernel development, Kernel functions, and maintenance, with recent Kernel versions. Experience of working with physical Embedded products development/Devices/automotive/IOT with connectivity, etc Vast experience with Embedded C, Embedded systems and a solid understanding of Linux operating systems. Strong skills in developing device drivers, and driver implementation, as well as device trees. Experience with systemd or other init systems. Strong skills in Embedded bootloaders such as (Das) U-Boot, Grub, BarBox, preferably on ARM-based systems. Experience of planning, shaping of requirements specification, and development for both new and existing products. Proficiency in C++. Rust or another system programming language is ideal. Skilful at debugging and profiling complex Embedded Linux systems. Expert knowledge of hardware electronics, circuit diagrams, and experience with Yocto Project or Buildroot, Logic analysers etc The senior Embedded Software Engineer is responsible for two key areas: the first involves Embedded core activities, such as new hardware bring-up and maintenance (enabling new features to work). The other part can be diverse, including security, peripheral drivers, display, and power, which are highly relevant. While it encompasses the entire product, the focus is often on Linux bootloaders or device drivers. When security is involved, it pertains to the hardware, boot, or Linux components. This role would be ideal for an experienced Linux Engineer who has worked with physical products in areas such as automotive, medical devices, IOT, tablets, mobile devices, or consumer-centric physical devices. This is an outstanding opportunity to join a recently formed London-based team for a fast-growing and successful European scaleup company with amazing customer-centric products and a strong software engineering culture, excellent benefits, and a balanced approach to work-life balance. The role involves approximately two-thirds of trips a year within Europe to collaborate with the European engineering team, and great opportunities to progress with an ambitious product-centric business. Opus Resourcing acts as an employment agency with respect to permanent employment.
FINTEC recruit is seeking an Embedded Software Engineer for our global subsea /marine client based in Aberdeen. This is a permanent role with salary £50,000 to £60,000 plus benefits, pension, private health care etc. Offering hybrid working options, flexi working, Monday to Friday with early finish on Fridays. You will be developing new medical monitoring equipment technologies used for marine/subsea/offshore work environments. Responsibilities: Software engineering input for existing and new systems and products Create documentation for specifications, proposals, test plans, reports etc Supporting software management of change for new & existing codebase Skills and experience required for the Embedded Software role :- Degree qualified in either Computer Science / Software / Electrical/Electronic Engineering or equivalent Experience with developing medical/health monitoring equipment would be an advantage Experience in a software development / engineering role & with development life cycle Good knowledge in embedded software (MPLAB, ST32) development, test and debug. Good knowledge in high level development languages preferably one or more of C# and C++, and C. Software management systems (e.g. Azure DevOps, GitHub, etc) and advantage Source code version control systems (specifically git) an advantage. Communications (network and serial) an advantage. User interface design, Database development & software design methodology is an advantage Haven an interest in interest in IOT devices and wireless communication protocols (Bluetooth Low Energy, Wi-Fi). Full details of the Embedded Software Engineer role is available on application. To apply please submit your current CV or apply via our FINTEC recruit website.
Sep 03, 2025
Full time
FINTEC recruit is seeking an Embedded Software Engineer for our global subsea /marine client based in Aberdeen. This is a permanent role with salary £50,000 to £60,000 plus benefits, pension, private health care etc. Offering hybrid working options, flexi working, Monday to Friday with early finish on Fridays. You will be developing new medical monitoring equipment technologies used for marine/subsea/offshore work environments. Responsibilities: Software engineering input for existing and new systems and products Create documentation for specifications, proposals, test plans, reports etc Supporting software management of change for new & existing codebase Skills and experience required for the Embedded Software role :- Degree qualified in either Computer Science / Software / Electrical/Electronic Engineering or equivalent Experience with developing medical/health monitoring equipment would be an advantage Experience in a software development / engineering role & with development life cycle Good knowledge in embedded software (MPLAB, ST32) development, test and debug. Good knowledge in high level development languages preferably one or more of C# and C++, and C. Software management systems (e.g. Azure DevOps, GitHub, etc) and advantage Source code version control systems (specifically git) an advantage. Communications (network and serial) an advantage. User interface design, Database development & software design methodology is an advantage Haven an interest in interest in IOT devices and wireless communication protocols (Bluetooth Low Energy, Wi-Fi). Full details of the Embedded Software Engineer role is available on application. To apply please submit your current CV or apply via our FINTEC recruit website.
IT Support Technician Derbyshire Permanent to £28,000 (DOE) IT Support Technician needed for a permanent position based in Derbyshire around 8 miles north of Derby (A38 Corridor). A chance to join an established and growing business with a proven track record in their industry. Start ideally Sept/Oct 2025. Key experience + responsibilities will include: Resolving IT incidents to 2nd line level + managing IT support requests from end-users. Supporting IT projects including software/hardware upgrades + rollouts. Setting up end-user hardware using imaging and automated Device Management systems. Escalating more complex issues to 3rd Line IT Support Engineers + 3rd party IT suppliers. Using IT Helpdesk logging systems + remote support tools. Full UK Driving Licence and own vehicle preferred. Technical Environment: Office 365, Windows, Active Directory, Mobile Devices (iPads/iPhones), Printers, TCP/IP, Networking, Fixed-Line (ADSL/Fibre/3G/4G). Benefits: Salary to £28k (DOE) + 25 days Holiday (+ BHs) + Pension + Life Assurance + BUPA Medical + Dental + Training & Professional Development.
Sep 02, 2025
Full time
IT Support Technician Derbyshire Permanent to £28,000 (DOE) IT Support Technician needed for a permanent position based in Derbyshire around 8 miles north of Derby (A38 Corridor). A chance to join an established and growing business with a proven track record in their industry. Start ideally Sept/Oct 2025. Key experience + responsibilities will include: Resolving IT incidents to 2nd line level + managing IT support requests from end-users. Supporting IT projects including software/hardware upgrades + rollouts. Setting up end-user hardware using imaging and automated Device Management systems. Escalating more complex issues to 3rd Line IT Support Engineers + 3rd party IT suppliers. Using IT Helpdesk logging systems + remote support tools. Full UK Driving Licence and own vehicle preferred. Technical Environment: Office 365, Windows, Active Directory, Mobile Devices (iPads/iPhones), Printers, TCP/IP, Networking, Fixed-Line (ADSL/Fibre/3G/4G). Benefits: Salary to £28k (DOE) + 25 days Holiday (+ BHs) + Pension + Life Assurance + BUPA Medical + Dental + Training & Professional Development.
Embedded Software Engineer (senior and mid-level) Hybrid - 50/50 Home and Office (Capenhurst) Join a global, independent provider of end-to-end power engineering solutions, supporting clients in managing and operating electrical networks. This is a well-established, innovation-led organisation with a strong, values-driven culture. About the Role You'll play a key role in developing cutting-edge embedded software for advanced measurement technologies used in the power industry. Working in a friendly and supportive team, you'll have the chance to contribute to real innovation. Key Responsibilities: Design and develop embedded software solutions for next-generation measurement devices Bring up firmware on newly developed in-house hardware platforms Implement software modules that enable embedded devices to communicate with cloud services Write clean, maintainable, and robust code that adheres to industry standards Continuously seek to improve product quality and development processes as product deployment scales What We're Looking For: Strong experience in C/C++ , including modern standards ( C++ 11/14/17 ) Proven experience in embedded software design and full lifecycle product development Solid understanding of low-level communication protocols ( SPI, I2C, RS232 ) and experience with ARM Cortex microprocessors Experience with unit testing frameworks and Git or similar version control systems Comfortable working in Linux as both a development and target platform Adaptability and a proactive mindset, with experience working in Agile environments Experience with Continuous Integration tools is a plus Awareness of the electricity or power industry is a bonus Benefits include: Holidays: 25 days of annual leave (FTE), plus bank holidays, with an extra day for every three years completed (up to a maximum of 30 days). Ability to buy an additional 5 days. Pension contributions of 8% from the employer (or cash equivalent). Comprehensive benefits, including Group Life Insurance, Income Protection, and Critical Illness cover (or cash equivalents). Private Medical Insurance (single cover or cash equivalent).
Sep 02, 2025
Full time
Embedded Software Engineer (senior and mid-level) Hybrid - 50/50 Home and Office (Capenhurst) Join a global, independent provider of end-to-end power engineering solutions, supporting clients in managing and operating electrical networks. This is a well-established, innovation-led organisation with a strong, values-driven culture. About the Role You'll play a key role in developing cutting-edge embedded software for advanced measurement technologies used in the power industry. Working in a friendly and supportive team, you'll have the chance to contribute to real innovation. Key Responsibilities: Design and develop embedded software solutions for next-generation measurement devices Bring up firmware on newly developed in-house hardware platforms Implement software modules that enable embedded devices to communicate with cloud services Write clean, maintainable, and robust code that adheres to industry standards Continuously seek to improve product quality and development processes as product deployment scales What We're Looking For: Strong experience in C/C++ , including modern standards ( C++ 11/14/17 ) Proven experience in embedded software design and full lifecycle product development Solid understanding of low-level communication protocols ( SPI, I2C, RS232 ) and experience with ARM Cortex microprocessors Experience with unit testing frameworks and Git or similar version control systems Comfortable working in Linux as both a development and target platform Adaptability and a proactive mindset, with experience working in Agile environments Experience with Continuous Integration tools is a plus Awareness of the electricity or power industry is a bonus Benefits include: Holidays: 25 days of annual leave (FTE), plus bank holidays, with an extra day for every three years completed (up to a maximum of 30 days). Ability to buy an additional 5 days. Pension contributions of 8% from the employer (or cash equivalent). Comprehensive benefits, including Group Life Insurance, Income Protection, and Critical Illness cover (or cash equivalents). Private Medical Insurance (single cover or cash equivalent).
Business Development Manager Engineering Location: Northwest England Job Type: Full-Time, Permanent. Salary: £47,000 - £57,000 DOE About the Role On behalf of our client, a leading UK-based precision engineering company specialising in CNC machining, we are seeking a Business Development Manager to join their growing commercial team. This is a fantastic opportunity for an experienced and technically minded sales professional to drive strategic growth across sectors such as aerospace, automotive, medical, and industrial manufacturing. The role requires a balance of commercial acumen and technical understanding, with a focus on building long-term client relationships and expanding market presence. Key Responsibilities New Business Development Identify and target new business opportunities across key industries Conduct market research and competitor analysis to guide outreach strategies Generate and manage a strong pipeline of prospects through networking, direct outreach, and events Client Relationship Management Build and nurture strong relationships with OEMs, Tier 1 suppliers, and engineering firms Understand technical requirements and deliver tailored CNC machining solutions Act as the key liaison between customers and internal engineering/production teams Sales Strategy & Execution Develop and execute strategic sales plans to meet growth and revenue targets Prepare and present commercial proposals and close new business deals Maintain accurate CRM records and report on sales activity and forecasts Technical Consultation Communicate technical capabilities, tolerances, and machining limitations to clients Collaborate with internal teams to align client needs with production feasibility Support customers with pre-sales technical advice and post-sale support Marketing & Industry Engagement Represent the company at trade shows, exhibitions, and industry networking events Contribute to marketing initiatives including brochures, digital campaigns, and case studies Required Experience & Qualifications 5+ years in sales, business development, or account management within CNC machining, precision engineering, or related manufacturing fields Strong technical understanding of CNC processes, materials, tolerances, and production workflows Proven track record of developing new business and managing the full sales cycle Excellent interpersonal, negotiation, and presentation skills Proficiency with CRM software and Microsoft Office Suite Full UK driving licence and willingness to travel regionally/nationally Desirable Attributes Hands-on background or training in CNC machining or mechanical engineering Established network within sectors such as aerospace, automotive, or medical devices Results-driven, self-motivated, and capable of working independently Customer-focused mindset with a consultative sales approach Compensation & Benefits Company vehicle or travel allowance Laptop and mobile phone Private pension scheme (post-probation) 28 days annual leave (including bank holidays) + additional company holidays Birthday off + professional development opportunities If you would like to apply for the role of Accounts Payable Clerk then please email your CV to (url removed) or call Jade on (phone number removed) Closing date is 21.09.2025 - Please note this could change subject to suitable applications Hawk 3 Talent Solutions are acting as an employment agency on behalf of its client. By applying for the above position and providing your personal data to us you understand that your data will be processed in line with our Privacy Policy. To view our full Privacy Policy please visit our website. Hawk 3 Talent Solutions are committed to the selection, recruitment and development of the best people, basing judgements solely on suitability for the job. Whilst we endeavour to respond to all applications individually, due to high volumes, this is not always possible. Thank you for your interest in this role and we look forward to working with you in the future
Sep 01, 2025
Full time
Business Development Manager Engineering Location: Northwest England Job Type: Full-Time, Permanent. Salary: £47,000 - £57,000 DOE About the Role On behalf of our client, a leading UK-based precision engineering company specialising in CNC machining, we are seeking a Business Development Manager to join their growing commercial team. This is a fantastic opportunity for an experienced and technically minded sales professional to drive strategic growth across sectors such as aerospace, automotive, medical, and industrial manufacturing. The role requires a balance of commercial acumen and technical understanding, with a focus on building long-term client relationships and expanding market presence. Key Responsibilities New Business Development Identify and target new business opportunities across key industries Conduct market research and competitor analysis to guide outreach strategies Generate and manage a strong pipeline of prospects through networking, direct outreach, and events Client Relationship Management Build and nurture strong relationships with OEMs, Tier 1 suppliers, and engineering firms Understand technical requirements and deliver tailored CNC machining solutions Act as the key liaison between customers and internal engineering/production teams Sales Strategy & Execution Develop and execute strategic sales plans to meet growth and revenue targets Prepare and present commercial proposals and close new business deals Maintain accurate CRM records and report on sales activity and forecasts Technical Consultation Communicate technical capabilities, tolerances, and machining limitations to clients Collaborate with internal teams to align client needs with production feasibility Support customers with pre-sales technical advice and post-sale support Marketing & Industry Engagement Represent the company at trade shows, exhibitions, and industry networking events Contribute to marketing initiatives including brochures, digital campaigns, and case studies Required Experience & Qualifications 5+ years in sales, business development, or account management within CNC machining, precision engineering, or related manufacturing fields Strong technical understanding of CNC processes, materials, tolerances, and production workflows Proven track record of developing new business and managing the full sales cycle Excellent interpersonal, negotiation, and presentation skills Proficiency with CRM software and Microsoft Office Suite Full UK driving licence and willingness to travel regionally/nationally Desirable Attributes Hands-on background or training in CNC machining or mechanical engineering Established network within sectors such as aerospace, automotive, or medical devices Results-driven, self-motivated, and capable of working independently Customer-focused mindset with a consultative sales approach Compensation & Benefits Company vehicle or travel allowance Laptop and mobile phone Private pension scheme (post-probation) 28 days annual leave (including bank holidays) + additional company holidays Birthday off + professional development opportunities If you would like to apply for the role of Accounts Payable Clerk then please email your CV to (url removed) or call Jade on (phone number removed) Closing date is 21.09.2025 - Please note this could change subject to suitable applications Hawk 3 Talent Solutions are acting as an employment agency on behalf of its client. By applying for the above position and providing your personal data to us you understand that your data will be processed in line with our Privacy Policy. To view our full Privacy Policy please visit our website. Hawk 3 Talent Solutions are committed to the selection, recruitment and development of the best people, basing judgements solely on suitability for the job. Whilst we endeavour to respond to all applications individually, due to high volumes, this is not always possible. Thank you for your interest in this role and we look forward to working with you in the future
Optical Systems Engineer - Medical Devices - Cambridge Following continued growth, a Medical Devices organisation is currently recruiting for someone to come into the team and focus on the optical systems design. Based in Cambridge, working with mechanical engineers, electronics engineers and software engineers to develop their life-improving medical devices. As you will be focusing on optical systems design, it is expected that you have been working as an optical physicist, optical engineer, optical systems engineer, optical systems designer, opto-mechanical engineer or another role that has involved you in working on optical systems designing, prototyping, and testing of new medical devices. You will be developing a range of medical technologies, so you will need to be able to use optical design tools such as Zemax, Code-V, OSLO, FRED or another similar technology. Due to the collaborative nature of the work, you will need to be able to communicate your ideas and project updates clearly and concisely. We are looking at various levels of industry experience, from PhD entry through to someone who has 15-20 years of experience. We expect you to hold a degree within a subject that led you into optical systems design roles. Master's and PhD education would also be beneficial, but not essential. In addition to working on industry-changing technologies, you will be offered a proven career development plan, continuous training to keep you at the forefront of the medical devices sector, excellent salary, bonus, enhanced pension, medical insurance, free meals and other excellent benefits you'd expect from a multinational blue-chip organisation. If you need to relocate to Cambridge, there are relocation packages that are negotiated on a case-by-case basis. We anticipate strong interest in this position, so apply now to ensure consideration. For more information, please contact Andrew Welsh, Director of Medical Devices, Biotech and Drug Discovery Recruitment at Newton Colmore, on (phone number removed). Alternatively, submit your application and a member of our team will be in touch. Please note that without a CV, we can only provide limited information.
Sep 01, 2025
Full time
Optical Systems Engineer - Medical Devices - Cambridge Following continued growth, a Medical Devices organisation is currently recruiting for someone to come into the team and focus on the optical systems design. Based in Cambridge, working with mechanical engineers, electronics engineers and software engineers to develop their life-improving medical devices. As you will be focusing on optical systems design, it is expected that you have been working as an optical physicist, optical engineer, optical systems engineer, optical systems designer, opto-mechanical engineer or another role that has involved you in working on optical systems designing, prototyping, and testing of new medical devices. You will be developing a range of medical technologies, so you will need to be able to use optical design tools such as Zemax, Code-V, OSLO, FRED or another similar technology. Due to the collaborative nature of the work, you will need to be able to communicate your ideas and project updates clearly and concisely. We are looking at various levels of industry experience, from PhD entry through to someone who has 15-20 years of experience. We expect you to hold a degree within a subject that led you into optical systems design roles. Master's and PhD education would also be beneficial, but not essential. In addition to working on industry-changing technologies, you will be offered a proven career development plan, continuous training to keep you at the forefront of the medical devices sector, excellent salary, bonus, enhanced pension, medical insurance, free meals and other excellent benefits you'd expect from a multinational blue-chip organisation. If you need to relocate to Cambridge, there are relocation packages that are negotiated on a case-by-case basis. We anticipate strong interest in this position, so apply now to ensure consideration. For more information, please contact Andrew Welsh, Director of Medical Devices, Biotech and Drug Discovery Recruitment at Newton Colmore, on (phone number removed). Alternatively, submit your application and a member of our team will be in touch. Please note that without a CV, we can only provide limited information.
Senior Systems Engineer - Biotech Platform Development - Cambridge A cutting-edge biotech company, based in Cambridge, are currently recruiting for a Senior Systems Engineer who will play a pivotal role in the development and delivery of next-generation medical diagnostics and biomanufacturing platforms. This is an opportunity to take technical ownership of complex, multidisciplinary systems and contribute to the translation of breakthrough IP into scalable, regulated products. You'll be working across engineering and R&D teams to support the design, integration, and commercialisation of semiconductor-based and biocomputing technologies. Your role will span product architecture, documentation to ISO 13485 standards, and hands-on delivery of systems that combine hardware, software, and biology. You'll collaborate with internal stakeholders and external partners to align technical execution with broader programme goals. We're looking for someone with experience in systems engineering, product development, or technical project delivery within biotech, diagnostics, or medical devices. You'll bring a solid understanding of regulated product development, and ideally some exposure to startup environments, IP creation, or cross-functional team collaboration. A background in mechanical, biomedical, or electronic engineering would be ideal. In return, you will receive a competitive salary, annual bonus, private healthcare, generous pension contributions, and access to a wide range of lifestyle and professional development benefits. This is a chance to join a company that values innovation, technical depth, and collaborative culture. You'll be supported by experienced leaders and given space to grow into broader responsibilities as the company scales. To learn more, contact Andrew Welsh, Director of Medical Devices, Biotech and Drug Discovery Recruitment at Newton Colmore, on (phone number removed). Alternatively, submit your CV and a member of our team will be in touch.
Sep 01, 2025
Full time
Senior Systems Engineer - Biotech Platform Development - Cambridge A cutting-edge biotech company, based in Cambridge, are currently recruiting for a Senior Systems Engineer who will play a pivotal role in the development and delivery of next-generation medical diagnostics and biomanufacturing platforms. This is an opportunity to take technical ownership of complex, multidisciplinary systems and contribute to the translation of breakthrough IP into scalable, regulated products. You'll be working across engineering and R&D teams to support the design, integration, and commercialisation of semiconductor-based and biocomputing technologies. Your role will span product architecture, documentation to ISO 13485 standards, and hands-on delivery of systems that combine hardware, software, and biology. You'll collaborate with internal stakeholders and external partners to align technical execution with broader programme goals. We're looking for someone with experience in systems engineering, product development, or technical project delivery within biotech, diagnostics, or medical devices. You'll bring a solid understanding of regulated product development, and ideally some exposure to startup environments, IP creation, or cross-functional team collaboration. A background in mechanical, biomedical, or electronic engineering would be ideal. In return, you will receive a competitive salary, annual bonus, private healthcare, generous pension contributions, and access to a wide range of lifestyle and professional development benefits. This is a chance to join a company that values innovation, technical depth, and collaborative culture. You'll be supported by experienced leaders and given space to grow into broader responsibilities as the company scales. To learn more, contact Andrew Welsh, Director of Medical Devices, Biotech and Drug Discovery Recruitment at Newton Colmore, on (phone number removed). Alternatively, submit your CV and a member of our team will be in touch.
Are you passionate about quality and precision? Join our client with this engineering role and help ensure top-tier standards every day. Proclinical is seeking a skilled engineer to join a dynamic team in Cambridge, UK. In this role, you will provide expertise in design control and risk management for medical devices and combination products throughout their lifecycle. You will collaborate with cross-functional teams to ensure compliance with quality and regulatory standards while supporting clinical trials and commercial licensures. This is an exciting opportunity to contribute to innovative biotherapeutic solutions. Responsibilities: Lead design control and risk management activities for combination product development programs. Author, review, and maintain design history files and risk management documentation. Facilitate risk management activities with external design companies and manufacturing facilities. Ensure compliance with internal and external quality and regulatory standards. Support design validation processes, including human factors engineering assessments. Assess external design companies and suppliers for quality systems and capabilities. Investigate device design and manufacturing issues from clinical trials and commercial use. Contribute to regulatory submission data and content for assigned projects. Support internal and external audits of the Quality Management System. Identify and implement strategies to improve combination product systems. Key Skills and Requirements: Background in science or engineering (e.g., chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, or related disciplines). Expertise in ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and EU Medical Devices Regulation. Experience in design controls and risk management for combination products. Familiarity with Human Factors Engineering and usability engineering principles. Knowledge of device assembly and manufacturing processes. Strong analytical skills for complex data analysis. Proficiency in project management methodologies and technical leadership. Excellent communication and collaboration skills. Proficiency in general computer software (e.g., word processing, spreadsheets, presentations). Understanding of Good Manufacturing Practices (GMP). If you are having difficulty in applying or if you have any questions, please contact Dean Fisher at (url removed). If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page. Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - (url removed)
Sep 01, 2025
Contractor
Are you passionate about quality and precision? Join our client with this engineering role and help ensure top-tier standards every day. Proclinical is seeking a skilled engineer to join a dynamic team in Cambridge, UK. In this role, you will provide expertise in design control and risk management for medical devices and combination products throughout their lifecycle. You will collaborate with cross-functional teams to ensure compliance with quality and regulatory standards while supporting clinical trials and commercial licensures. This is an exciting opportunity to contribute to innovative biotherapeutic solutions. Responsibilities: Lead design control and risk management activities for combination product development programs. Author, review, and maintain design history files and risk management documentation. Facilitate risk management activities with external design companies and manufacturing facilities. Ensure compliance with internal and external quality and regulatory standards. Support design validation processes, including human factors engineering assessments. Assess external design companies and suppliers for quality systems and capabilities. Investigate device design and manufacturing issues from clinical trials and commercial use. Contribute to regulatory submission data and content for assigned projects. Support internal and external audits of the Quality Management System. Identify and implement strategies to improve combination product systems. Key Skills and Requirements: Background in science or engineering (e.g., chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, or related disciplines). Expertise in ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and EU Medical Devices Regulation. Experience in design controls and risk management for combination products. Familiarity with Human Factors Engineering and usability engineering principles. Knowledge of device assembly and manufacturing processes. Strong analytical skills for complex data analysis. Proficiency in project management methodologies and technical leadership. Excellent communication and collaboration skills. Proficiency in general computer software (e.g., word processing, spreadsheets, presentations). Understanding of Good Manufacturing Practices (GMP). If you are having difficulty in applying or if you have any questions, please contact Dean Fisher at (url removed). If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page. Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - (url removed)
Job Title: Design Control and Risk Management Compliance Engineer Contract: 12 months Hours:37 hrs p/w Location: Cambridge Pay rate: up to 20.79 p/h DOE Role overview This position is in the Biotherapeutics Pharmaceutical Research and Development (Drug Product Design and Development) located in Cambridge, UK. The incumbent will provide design control and risk management subject matter expertise to medical device combination product development programmes throughout the product lifecycle. This will involve ensuring consistent implementation of applicable processes and standards across the portfolio, in addition to the facilitation and documentation of specific design control and risk management activities, whilst interacting with cross functional development teams at all levels of the organisation. Primary Duties: Lead design control and risk management activities for medical device combination product development programmes, ensuring deliverables are appropriately authored, approved, and maintained to support clinical trials and commercial licensures. Support and facilitation of effective design control and risk management activities internally, at external design companies, and at the business manufacturing facilities/CMOs related to assigned projects. Generation, approval, and retention of business' design control and risk management documentation ensuring that quality and regulatory requirements are satisfied. Ensure medical device combination product design control and risk management activities are compliant with quality and regulatory standards, both internal and external. Provide input and support to design validation including, but not limited to, use-related risk assessments. Support the generation of all regulatory submission data and content for assigned medical device combination product projects. Support internal and external audits of the Biotherapeutics Pharmaceutical Research and Development Quality Management Systems. Organizational Relationships Device development teams - Drug Product leads, packaging engineers, medical device combination product engineers, device development leads, human factors SMEs, design engineers and device analytical scientists. Co-development team - drug product and device SMEs. Quality Assurance GCMC (Regulatory) PGS - manufacturing sites and post launch device team. External designers and contract manufacturing organizations. Education, Skills And Experience BSc in appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline) with a minimum of 5 years of relevant experience in the pharmaceutical combination product and/or device industries OR MSc in appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline) with a minimum of 5 years of relevant experience in the pharmaceutical combination product and/or device industries History of working in accordance with the requirements of ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation. Experience in design control for medical device combination products and/or medical devices Experience in risk management for medical device combination products and/or medical devices. Familiar with Human Factors Engineering - Usability Engineering. Familiar with device assembling manufacturing processes. Technical Skills Requirements Working knowledge of ISO 9001, ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation. Familiarity EN 62366, EN 60601, and EN 62304. Able to learn and apply established procedures in a reliable and consistent manner. Capable of working independently with minimal supervision. High level of attention to technical details and accuracy. Able to prioritize multiple responsibilities and to work on multiple tasks simultaneously. Able to work collaboratively in cross functional teams. Excellent communication (e.g., oral, written, presentation) and interpersonal relationship skills. Proficiency in general computer software such as word processing, spreadsheets, presentations. Understand Good Manufacturing Practices (GMP). Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Sep 01, 2025
Seasonal
Job Title: Design Control and Risk Management Compliance Engineer Contract: 12 months Hours:37 hrs p/w Location: Cambridge Pay rate: up to 20.79 p/h DOE Role overview This position is in the Biotherapeutics Pharmaceutical Research and Development (Drug Product Design and Development) located in Cambridge, UK. The incumbent will provide design control and risk management subject matter expertise to medical device combination product development programmes throughout the product lifecycle. This will involve ensuring consistent implementation of applicable processes and standards across the portfolio, in addition to the facilitation and documentation of specific design control and risk management activities, whilst interacting with cross functional development teams at all levels of the organisation. Primary Duties: Lead design control and risk management activities for medical device combination product development programmes, ensuring deliverables are appropriately authored, approved, and maintained to support clinical trials and commercial licensures. Support and facilitation of effective design control and risk management activities internally, at external design companies, and at the business manufacturing facilities/CMOs related to assigned projects. Generation, approval, and retention of business' design control and risk management documentation ensuring that quality and regulatory requirements are satisfied. Ensure medical device combination product design control and risk management activities are compliant with quality and regulatory standards, both internal and external. Provide input and support to design validation including, but not limited to, use-related risk assessments. Support the generation of all regulatory submission data and content for assigned medical device combination product projects. Support internal and external audits of the Biotherapeutics Pharmaceutical Research and Development Quality Management Systems. Organizational Relationships Device development teams - Drug Product leads, packaging engineers, medical device combination product engineers, device development leads, human factors SMEs, design engineers and device analytical scientists. Co-development team - drug product and device SMEs. Quality Assurance GCMC (Regulatory) PGS - manufacturing sites and post launch device team. External designers and contract manufacturing organizations. Education, Skills And Experience BSc in appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline) with a minimum of 5 years of relevant experience in the pharmaceutical combination product and/or device industries OR MSc in appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline) with a minimum of 5 years of relevant experience in the pharmaceutical combination product and/or device industries History of working in accordance with the requirements of ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation. Experience in design control for medical device combination products and/or medical devices Experience in risk management for medical device combination products and/or medical devices. Familiar with Human Factors Engineering - Usability Engineering. Familiar with device assembling manufacturing processes. Technical Skills Requirements Working knowledge of ISO 9001, ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation. Familiarity EN 62366, EN 60601, and EN 62304. Able to learn and apply established procedures in a reliable and consistent manner. Capable of working independently with minimal supervision. High level of attention to technical details and accuracy. Able to prioritize multiple responsibilities and to work on multiple tasks simultaneously. Able to work collaboratively in cross functional teams. Excellent communication (e.g., oral, written, presentation) and interpersonal relationship skills. Proficiency in general computer software such as word processing, spreadsheets, presentations. Understand Good Manufacturing Practices (GMP). Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
