Scientist II - Physical testing

SRG; Newbridge; On-site; GBP 35,000 - 50,000; Full time

Job summary

SRG is seeking a Scientist II for the Physical Testing department in Deeside. You will design and execute physical test programmes to support development of innovative medical devices in a regulated ISO- controlled laboratory environment.

You will contribute to method development, perform data analysis, draft validation protocols and reports, and ensure compliance with GMP, GLP and GDP. The role requires clear communication and collaboration across R&D and base‑business projects.

Qualifications

• 3 years of laboratory experience; medical devices/pharma experience preferred.
• Strong understanding of physical testing principles.
• Excellent written and verbal communication.
• Familiarity with ISO13485:2016, ISO9001, GMP guidelines is advantageous.

Responsibilities

• 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.
• Author validation protocols, reports and laboratory records.
• Independently analyse data and present laboratory findings.

Skills

Laboratory experience

Physical testing principles

Communication skills

Education

Bachelor's degree in a scientific discipline

Tools

Microsoft Word

Microsoft Excel

Minitab

Job description

Job Advert: Scientist II - Physical Testing

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 and 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).