Physical Testing Scientist — Medical Devices & GMP/GLP

SRG; Wales; On-site; GBP 28,000 - 40,000; Full time

Job summary

SRG is seeking a Scientist I–II in the Deeside area to support physical testing for medical devices. The role requires developing, validating and executing test methods, while ensuring GMP/GLP/GDP compliance and accurate data recording. Strong attention to detail and good communication are essential.

The position is full-time and onsite, with responsibilities spanning R&D support, data interpretation, and internal reporting. Experience with ISO and regulatory guidelines is advantageous.

Qualifications

• 1–2 years’ experience working in a laboratory environment.
• Understanding of safe working practices in a laboratory environment.
• Experience within the Medical Devices or Pharmaceutical industry.
• Knowledge and experience of GMP, GLP, GDP and quality regulations.

Responsibilities

• Design, plan and execute physical testing activities to support R&D and base business projects.
• Develop and validate new physical testing methods in line with industry standards.
• Estimate resource and time requirements for experiments and monitor performance to ensure targets are met.
• Assist with laboratory test method and procedural revisions.
• Independently analyse and interpret test data using statistical analysis tools.
• Author and technically approve validation protocols, reports, benchbooks, and technical documentation.
• Accurately record laboratory data in accordance with GDP requirements.
• Prepare and deliver internal presentations to communicate laboratory findings.

Skills

Laboratory techniques

Data analysis

Attention to detail

Communication skills

Problem solving

Education

Bachelor's Degree in a relevant science

Tools

Minitab

Microsoft Word

Microsoft Excel

Job description

SRG is seeking a Scientist I–II in the Deeside area to support physical testing for medical devices. The role requires developing, validating and executing test methods, while ensuring GMP/GLP/GDP compliance and accurate data recording. Strong attention to detail and good communication are essential.

The position is full-time and onsite, with responsibilities spanning R&D support, data interpretation, and internal reporting. Experience with ISO and regulatory guidelines is advantageous.