Scientist II; Physical Testing

Job Advert:
Scientist II – Physical Testing

Location: Deeside, UK (Onsite)

We are seeking a highly motivated Scientist II to join the Physical Testing Department, supporting the development of innovative medical devices. This role plays a critical part in ensuring product safety, efficacy, and quality through robust physical testing activities.

As a Scientist II, you will design and execute physical test programmes, contribute to method development, and support multiple projects within a regulated ISO‑controlled laboratory environment. This is an excellent opportunity to apply your laboratory experience, analytical mindset, and technical skills in a fast‑paced, collaborative setting.

• Work within an ISO 13485 and ISO 9001 laboratory quality system, following GxP procedures.
• Design, plan and execute physical testing to support R&D and base‑business projects.
• Develop and validate new physical test methods aligned with industry standards.
• Estimate resources and timelines for experiments, ensuring delivery against targets.
• Author technical documentation including validation protocols, reports and laboratory records.
• Independently analyse and interpret data, including statistical evaluation.
• Present laboratory findings through clear internal presentations.
• Ensure accurate documentation and data integrity in line with GMP, GLP and GDP.
• Conduct laboratory investigations, perform root cause analysis, and apply CAPA as needed.
• Support updates to laboratory methods, SOPs and processes.
• Maintain compliance with cGMP regulations, SOPs and technical documentation.
• Contribute to change control activities.
• Support daily laboratory operations such as housekeeping, equipment checks, calibration, preparing solutions, stock management, sample shipping and documentation scanning.

• 2–3 years’ experience in a laboratory environment; medical devices/pharmaceutical industry experience preferred.
• Strong understanding of physical testing principles.
• Excellent communication skills, both written and verbal.
• Good working knowledge of Microsoft Word and Excel.
• Understanding of compliance requirements including ISO
  13485:2016, ISO
  9001:2000, FDA 21 CFR part 820 and GMP guidelines.
• Familiarity with safe laboratory working practices; experience with statistical analysis and Minitab desirable.

• Bachelor’s degree in a relevant scientific discipline (e.g., Biological Sciences).