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Scientist II - Physical Testing

Job in Connah's Quay, Deeside, Flintshire, Wales, UK
Listing for: Convatec
Contract position
Listed on 2026-07-23
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Salary/Wage Range or Industry Benchmark: 34000 - 52000 GBP Yearly GBP 34000.00 52000.00 YEAR
Job Description & How to Apply Below
Position: Scientist II - Physical Testing - 1 year contract
Location: Connah's Quay

Job Description

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. The facilities will also strengthen our collaboration with Manchester’s vibrant life sciences ecosystem, which includes leading universities, hospitals, and research institutions.

Position Overview

A Scientist II in the Physical Testing Department supports the product development process for medical devices. The role requires a good understanding of the importance of physical testing in ensuring the safety, efficacy, and quality of medical devices. Responsibilities include conducting various tests and experiments, generating, documenting, and analysing data in compliance with Good Manufacturing Practices, Good Laboratory Practices, and Good Documentation Practices.

The role also involves developing test methods based on recognised industry standards or bespoke methods to satisfy product requirements. The Scientist must be detail oriented, able to work on multiple projects, adapt to changes, and possess strong problem‑solving and communication skills.

Key Responsibilities
  • Work within a controlled ISO 13485 and ISO 9001 laboratory quality system and in accordance with GxP procedures.
  • Design, plan and execute physical testing to support R&D activities and base business projects in accordance with applicable procedures and guidelines.
  • Develop and validate new physical testing methods.
  • Estimate the resources and time required to conduct an experiment and monitor performance to ensure targets are met.
  • Author validation protocols, reports and technical documents for medical devices/pharmaceutical products.
  • Independently analyse and interpret data through statistical analysis.
  • Prepare and present internal presentations to communicate laboratory findings.
  • Effectively organise assigned workload; ensure integrity of all data generated and timely/accurate provision of results to GLP standards.
  • Record and analyse laboratory data accurately in accordance with good documentation practices.
  • Perform detailed laboratory investigations to determine 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.
  • Ensure laboratory compliance with cGMP regulations and SOPs/TDs.
  • Participate in change control activities and associated actions.
  • Support laboratory daily activities such as housekeeping, equipment maintenance and calibration, solution preparation, consumable stock replenishment, sample shipping, scanning documentation, and sample logging.
Skills & Experience
  • 2–3 years experience in a working laboratory environment, with the Medical Devices/Pharmaceutical Industry preferred.
  • Good written and verbal communication skills.
  • Broad understanding of physical testing.
  • Good working knowledge of Microsoft Office, specifically Word and Excel.
  • Familiarity with safe work practices in a laboratory environment.
  • Working knowledge and understanding of compliance with FDA and European regulations relating to Quality Systems (ISO 13485:2016, ISO 9001:2000, FDA 21 CFR part 820) and GMP Guidelines and Regulation.
  • 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…

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