Medical Device Physical Testing Scientist II

SRG

Newbridge

On-site

GBP 36,000 - 43,000

Full time

10 days ago
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Job summary

SRG in Deeside is seeking a Scientist II – Physical Testing to support medical devices product development. The role involves designing and performing physical tests, documenting results and ensuring GMP/GLP/GDP compliance, with a focus on data integrity.

You will develop test methods, analyse data with statistics, and prepare validation reports while coordinating with R&D. The position is on-site for a 12-month contract, requiring 2–3 years lab experience and strong communication.

Qualifications

  • Bachelor’s Degree in a relevant science-related discipline (e.g., biological sciences).
  • 2-3 years in a working laboratory environment, preferably in Medical Devices/Pharmaceutical industry.
  • Good written and verbal communication skills.
  • Working knowledge of FDA/ISO regulatory requirements for Quality Systems and GMP guidelines.

Responsibilities

  • Design, plan and execute Physical Testing in support of R&D activities and base business projects.
  • Development and validation of new Physical Testing methods.
  • 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 findings.
  • Ensure data integrity and timely, GLP-compliant reporting.
  • Assist in lab method/procedural revisions and change control activities.
  • Support daily laboratory activities including equipment maintenance and sample handling.

Skills

Physical testing
Laboratory experience
Communication skills
MS Office
Regulatory compliance
Statistics (Minitab)
Safety in lab

Education

Bachelor's degree

Tools

Minitab

Job description

SRG in Deeside is seeking a Scientist II – Physical Testing to support medical devices product development. The role involves designing and performing physical tests, documenting results and ensuring GMP/GLP/GDP compliance, with a focus on data integrity.

You will develop test methods, analyse data with statistics, and prepare validation reports while coordinating with R&D. The position is on-site for a 12-month contract, requiring 2–3 years lab experience and strong communication.

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