Physical Testing Scientist

SRG; Newbridge; On-site; GBP 31,000 - 33,000; Full time

Job summary

SRG in Deeside (UK) is seeking a Scientist I – Physical Testing for a 12-month, onsite contract. The role supports the product development process for medical devices by conducting physical testing to ensure safety, efficacy, and quality.

Responsibilities include designing, executing, and documenting tests in line with GMP, GLP and GDP, developing test methods, analysing data, and contributing to CAPA investigations while maintaining rigorous data integrity and compliance standards.

Qualifications

• 1–2 years’ experience in a laboratory environment.
• Broad understanding of physical testing techniques.
• Good written and verbal communication skills.
• Strong organisational skills and attention to detail.
• Proficient in Microsoft Word and Excel.

Responsibilities

• Operate within ISO 13485 and ISO 9001 laboratory quality systems.
• Design, plan and execute physical testing activities for R&D and base business projects.
• Develop and validate new physical testing methods per industry standards.
• Analyse data using statistical tools and report findings.
• Prepare validation protocols, reports and benchbooks; document to GDP standards.
• Conduct investigations into out-of-specification results and implement CAPA actions.
• Support daily laboratory operations including equipment maintenance, stocking, and sample logging.

Education

Bachelor’s Degree in a relevant science

Job description

Job Title: Scientist I – Physical Testing

Location: Deeside, UK (Onsite)

Contract Length: 12 Months

Working Hours: Full Time – 35 hours per week

Pay Rate: £122.62 per day (PAYE)

Role Overview

The Scientist II in the Physical Testing Department supports the product development process for medical devices by conducting physical testing to ensure product safety, efficacy, and quality. The role involves generating, analysing, and documenting data in compliance with Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Documentation Practice (GDP).

Scientist II’s are expected to apply scientific knowledge and practical laboratory experience to develop, validate, and execute physical test methods based on recognised industry standards and bespoke product requirements. The role requires strong attention to detail, effective workload management across multiple projects, adaptability to change, and excellent problem‑solving and communication skills.

Key Responsibilities

Quality & Compliance

• Operate within a controlled ISO 13485 and ISO 9001 laboratory quality system.
• Ensure compliance with GxP, cGMP, SOPs and Technical Documents (TDs).
• Maintain data integrity and ensure accurate, timely reporting to GLP standards.
• Participate in change control activities and associated actions.

Physical Testing & Method Development

• 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.

Data Analysis & Documentation

• 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.

Investigations & Continuous Improvement

• Conduct detailed laboratory investigations into atypical or out-of-specification (OOS) results.
• Perform root cause analysis and implement corrective and preventative actions (CAPA).
• Author clear, concise investigation reports.

Laboratory Operations Support

• Support daily laboratory activities, including:
• Housekeeping
• Equipment maintenance and calibration
• Solution preparation
• Consumable stock replenishment
• Sample shipping and logging
• Document scanning and filing

Authority

Quality Management System Authority

For Physical Testing‑related protocols, plans, reports, benchbooks and test data, the Scientist II has authority as:

• Author Approver
• Technical Approver

Skills & Experience

Essential

• 1–2 years’ experience working in a laboratory environment.
• Broad understanding of physical testing techniques.
• Good written and verbal communication skills.
• Strong organisational skills and attention to detail.
• Good working knowledge of Microsoft Word and Excel.
• Understanding of safe working practices in a laboratory environment.

Desirable

• Experience within the Medical Devices or Pharmaceutical industry.
• Working knowledge of FDA and European quality regulations, including:
• ISO 13485:2016
• ISO 9001
• FDA 21 CFR Part 820
• Knowledge and experience of GMP guidelines and regulations.
• Statistical analysis experience, with Minitab desirable.

Qualifications / Education

• Bachelor’s Degree in a relevant science‑related discipline (e.g. biological sciences).