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Holt, Cymru / Wales, United Kingdom
Onsite
Convatec has announced a major milestone in our R&D journey and commitment to our vision of pioneering trusted medical solutions to improve the lives we touch. We have unveiled plans to relocate the majority of our UK-based research and development (R&D) activities from Deeside to Manchester from late 2027/early 2028, alongside a significant expansion of our facilities in Boston.
An exciting future in Manchester
The new, planned Manchester facility has the potential to be a major R&D hub in our global network which will initially function as the company’s global testing laboratories, with cutting-edge analytical R&D capabilities including quality control and materials, regulatory functions, and health innovation, positioning Convatec at the forefront of medical technology development. Our new state-of-the-art facilities will also strengthen our collaboration with Manchester’s vibrant life sciences ecosystem, which includes leading universities, hospitals, and research institutions
To perform analytical testing on existing and new medical devices, skin care products and raw materials according to pre-determined protocols, SOPs, OCIs and TDs in support of product claims. To support business units in the method design, development, and validation of new analytical test methods upon request.
Key Responsibilities:
Maintain compliance to ISO13485 and ISO9001 standards in accordance with GLP/GMP compliant procedures.
Analysing, documenting, interpreting, and reporting laboratory data to GMP/GLP standards.
Collation and reporting of laboratory data in technical reports.
Assist with the drafting of new analytical methods for new products and/or techniques.
Maintenance, calibration, documentation and updating quality records for the Analytical Laboratory.
Support planned and ad-hoc analytical testing/test method development and support laboratory tasks as and when required.
Perform laboratory/OOS investigations with some supervision incorporating problem-solving and troubleshooting for future improvements.
Ensure the Analytical labs are maintained as a safe working environment, raising near misses where needed.
Experience with a wide range of analytical equipment such as balances and pipettes through to HPLC and ICP-MS.
Use of basic (e.g., Microsoft Word, Excel, SAP, etc.) and advanced (e.g., Waters Empower, ChemStation, Masshunter, Minitab etc.) software packages for ordering goods, data collection, analysis, statistical manipulation etc.
Responsible for the ordering of laboratory consumables, chemicals, reagents and equipment when required.
Act as support for other R&D groups with laboratory testing where required.
Liaise with external vendors via telephone and when on-site including arranging of service contracts as well as the maintenance, servicing, and calibration of equipment.
Actively execute improvement ideas (Lean/6S) for the Analytical Laboratory and other owned areas.
Support improvements to current Analytical processes including updates to current test and operating procedures.
Skills & Experience:
Preferably 1-2 years’ experience working in Medical Device/Pharmaceutical Industry within an R&D/product development role.
Good working knowledge of laboratory Health and Safety Practices.
Competent in basic and some advanced chemistry and laboratory techniques.
Competent in following and adhering to SOPs, OCIs and TDs.
A drive to understand the process of executing method validation for new products and raw materials.
Basic experience in the utilisation of computerised systems to manage data and information.
Good working knowledge of Microsoft Office - specifically Word and Excel.
Understanding of compliance with FDA and European Regulations (ICH), Quality Systems and GMP Guidelines.
Disciplined in adhering to group objectives including taking an active role in team collaborative activities.
Qualifications/Education:
B.Sc., or equivalent in a scientific discipline – analytical chemistry desirable.
Working Conditions
Working in a laboratory environment with exposure to chemicals, reagents, and solvents.
Competent in the disposal of chemicals, reagents, and solvents in accordance with site and environmental procedures.
Ability to react and respond positively to changes in priority and workload including the ability to balance multiple, competing priorities to meet objectives.
Use of VDU equipment.
Special Factors
Flexibility of task management and working laboratory environment is essential due to changes in business priorities and product launches.
Ready to join us?
At Convatec we're pioneering trusted medical solutions to improve the lives we touch. If you're ready to make a real impact, apply today and help us bring our Forever Caring promise to life.
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Equal opportunities
Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
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About Convatec
Pioneering trusted medical solutions to improve the lives we touch:
Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With over 10,000 colleagues, we provide products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention, treatment for hard to heal wounds, at-risk skin and ulcerated tissue to supporting debilitating conditions, improved patient outcomes and reduced care costs. Convatec's revenues in 2025 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit: http://www.convatecgroup.com.