Scientist I - Physical Testing – 1 year contract

Convatec; Manchester; On-site; GBP 28,000 - 38,000; Full time

Job summary

Convatec is relocating UK R&D activities from Deeside to Manchester, expanding capabilities in analytical R&D and quality control. The Scientist I will support physical testing, ensure GMP/GLP compliance, and generate data for medical devices.

The role emphasizes meticulous experimentation, data integrity, and cross-functional collaboration across EU/UK teams. The position is based onsite in the UK with potential occasional remote work, reporting to the Physical Testing Department.

Qualifications

• Graduate/entry level with familiarity of safe working in a laboratory environment.
• Experience in a working laboratory environment within Medical Devices/Pharmaceutical Industry is preferred.
• Good written and verbal communication skills.

Responsibilities

• Perform/plan physical testing to support R&D and base business projects.
• Design, plan and execute testing in accordance with procedures and guidelines.
• Develop and validate new physical testing methods.
• Estimate resources and time for experiments and monitor performance.
• Author validation protocols, reports and technical documents for medical devices.
• Perform basic statistical analysis of test data.
• Ensure data integrity and GLP/GMP/GDP compliance.
• Contribute to investigations and root cause analyses.

Skills

Lab safety

Data analysis

Communication

MS Office

Education

Bachelor’s Degree in a relevant science

Tools

MiniTab

Job description

Reponsible for conducting and/or managing scientific research or quality testing performed in a laboartory environment including:

• Setting up, configuring, checking safety, installing, and maintaining laboratory equipment
• Planning, designing, conducting or following procedures within laboratory experiments to test the physical and/or chemical specifications of various substances, materials, and products to inform scientific research
• Estimating the resources and time required to conduct an experiment and monitoring performance to ensure these targets are met
• Collecting, preparing, and testing samples and recording observations
• Compiling research data and reporting results including with recommendations, applications, and conclusions
• Ensuring experiments and analyses are conducted within budgets and according to established scientific standards
• Researching, evaluating, and recommending investments in technology, equipment, systems, or other assets that will enhance the laboratory’s performance

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.

A Scientist I in the Physical Testing Department supports the product development process for medical devices. Scientists should have a good understanding of the importance of physical testing in ensuring the safety, efficacy, and quality of medical devices. Scientists are responsible for conducting various tests and experiments to assess the physical properties of medical devices. Scientists will generate, document and analyse data in compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and Good Documentation Practices (GDP). Scientists should be detail-oriented, able to work on multiple projects and adapt to changes, with good problem-solving skills and strong communication are essential.

Key responsibilities

• Working within a controlled ISO 13485 and ISO 9001 laboratory quality system and in accordance with GxP procedures.
• Design, plan and execute Physical Testing in support of R&D activities and base business projects in accordance with applicable procedures and guidelines.
• Development and validation of new Physical Testing methods.
• Estimating the resources and time required to conduct an experiment and monitoring performance to ensure targets are met.
• Author validation protocols, reports and technical documents for medical devices/pharmaceutical products.
• Perform basic statistical analysis of test data.
• Prepare and present internal presentations to present findings of the laboratory.
• Effective organisation of assigned workload; ensures integrity of all data generated and timely/accurate provision of results to GLP standards.
• Accurate recording and analysis of laboratory data in accordance with good documentation practices.
• Perform detailed laboratory investigations to determine the root cause analysis of atypical and out of specification results, apply corrective and preventative actions and author concise investigation reports.
• Assist in laboratory test method/procedural revisions.
• Ensures laboratory compliance with cGMP regulations and SOP’s/TD’s.
• Involvement in change control activities and associated actions.
• Support laboratory daily activities such as laboratory housekeeping, equipment maintenance and calibration, solution preparation, consumable stock replenishment, shipping samples, scanning documentation, logging of samples etc.

Skills & Experience

• Graduate/entry level. Familiarity with safe working in a laboratory environment. Experience in a working laboratory environment, within Medical Devices / Pharmaceutical Industry is preferred.
• Good written and verbal communication skills.
• Good working knowledge of Microsoft Office, specifically Word and Excel.
• Working knowledge and understanding of compliance with FDA and European regulations relating to Quality Systems (ISO13485:2016, ISO9001:2000, FDA 21 CFR part 820) and GMP Guidelines and Regulation.
• A detailed understanding of common statistical analysis and experience with MiniTab desirable.

Qualifications/Education

• Bachelor’s Degree in a relevant science-related discipline, i.e., biological sciences.

Working Conditions

This position is based in Deeside (UK) working within an office and laboratory environment. This is an onsite position with the opportunity to occasionally remote work as an when agreed in advance with their manager.

• Working in a laboratory environment with exposure to biological agents, chemicals and reagents – Training will be provided.
• Competent in the disposal of chemicals and reagents in accordance with site and local environmental procedures – Training will be provided.
• Health and Safety at Work etc. Act 1974.
• The Management of Health and Safety at Work Regulations 1999.

Special Factors

Flexibility of task management and working laboratory environment is essential due to continually changing priorities. Convatec is a multi-national company therefore some flexibility in hours is required due to working in an international company with colleagues in different time zones.

Beware of scams online or from individuals claiming to represent Convatec

A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.

If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at [e-mail].

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.

Notice to Agency and Search Firm Representatives

Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

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.