Scientist II - Physical testing

SRG; Newbridge; On-site; GBP 6,642,000 - 7,934,000; Full time

Job summary

SRG is seeking a Scientist II for Deeside to lead physical testing activities in a regulated ISO environment. You will design and execute test programmes, develop methods, and support multiple projects with rigorous data analysis and clear documentation.

The role requires strong communication, lab experience, and familiarity with ISO13485/9001 and GMP guidelines, with a focus on quality and traceability in a fast-paced setting.

Qualifications

• 3 years’ experience in a laboratory environment.
• Experience in medical devices/pharmaceutical industry preferred.
• Familiarity with GMP/GDP/cGMP concepts.

Responsibilities

• Design, plan and execute physical testing to support R&D and base‑business projects.
• Author validation protocols, reports and lab records.
• Analyse and interpret data with statistical evaluation.
• Maintain ISO 13485 and ISO 9001 quality systems compliance.
• Support CAPA, change control, and investigations.
• Prepare solutions, manage stock, and ship samples.

Skills

Laboratory experience

Physical testing principles

Communication skills

Statistical analysis

Education

Bachelor's degree in Biological Sciences

Tools

Microsoft Word

Microsoft Excel

Minitab

Job description

Job Advert: Scientist II – Physical Testing

Contract: 12‑Month

Rate: £142.32 per day

Location: Deeside, UK (Onsite)

About the Role

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.

Key Responsibilities

• 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 & documentation scanning.

Skills & Experience

• 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 ISO13485:2016, ISO9001:2000, FDA 21 CFR part 820 and GMP guidelines.
• Familiarity with safe laboratory working practices; experience with statistical analysis and Minitab desirable.

Qualifications

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