Physical Testing Scientist II – Medical Devices

SRG; Wales; On-site; GBP 34,000 - 48,000; Full time

Job summary

SRG in the United Kingdom is seeking a Scientist II to support physical testing in the medical device development process. You will design, execute and validate testing methods, analyze data, and ensure GLP/GDP compliance while preparing documentation and reports.

The role requires strong communication skills and a solid understanding of GMP, ISO13485, and FDA regulations. You will work in a controlled lab environment within a multi-project setting in Wales.

Qualifications

• Bachelor’s degree in a science-related field is required.
• Experience in a laboratory environment with GMP/GLP knowledge is preferred.
• Good written and verbal communication skills are essential.
• Knowledge of ISO13485, ISO9001 and FDA regulations is desirable.
• Experience with statistical analysis tools (e.g., Minitab) is a plus.

Responsibilities

• Design, plan and execute Physical Testing in R&D and base projects.
• Develop and validate new Physical Testing methods.
• Record data and ensure GLP/GDP compliance.
• Author validation protocols, reports and technical documents.
• Analyze data statistically and present findings internally.
• Maintain lab organisation and data integrity per GMP standards.
• Contribute to change controls and SOP updates.
• Prepare lab materials, calibrations, and housekeeping tasks.
• Support daily lab activities and sample shipping.
• Ensure cGMP alignment in testing and documentation.

Skills

Written communication

Verbal communication

Physical testing concepts

Regulatory knowledge

Statistical analysis

Education

Bachelor’s Degree in a relevant science-related discipline

Tools

Microsoft Word

Microsoft Excel

Minitab

Job description

SRG in the United Kingdom is seeking a Scientist II to support physical testing in the medical device development process. You will design, execute and validate testing methods, analyze data, and ensure GLP/GDP compliance while preparing documentation and reports.

The role requires strong communication skills and a solid understanding of GMP, ISO13485, and FDA regulations. You will work in a controlled lab environment within a multi-project setting in Wales.