GMP/GDP Quality Release Specialist

Clinigen Group; Byfleet; On-site; GBP 42,000 - 56,000; Full time

Benefits offered by this job

27 days holiday plus 8 bank holidays

Pension contributions 4.5% matched

Life assurance 4 x annual salary

Flexible Benefits Platform with £25/月(

Annual salary review

Independent financial advice service

Enhanced Employee Assistance Programme

Shopping discounts with retailers

Long service awards

Recognition scheme & employee of the 


Job summary

Clinigen Group is seeking a proactive Quality Release Specialist to join our Quality and Warehouse teams in the UK. You will help maintain GMP and GDP compliance and support the QMS, ensuring product quality and patient safety across activities.

You will collaborate with cross‑functional partners, investigators and regulators to review quality records, author documentation, and drive continuous improvement within a fast‑paced, global pharmaceutical environment.

Qualifications

• Degree in Life Sciences, Pharmacy or Chemistry (or equivalent).
• Experience in a Quality Assurance or related role.
• Knowledge of GMP and GDP guidelines for human medicinal products.
• Understanding of WDA(H), MS and MIA(IMP) licence requirements.

Responsibilities

• Manage day-to-day activities within the Quality Management System (QMS).
• Create, review and approve quality documentation, including SOPs and forms.
• Maintain GMP and GDP standards, managing quality records.
• Investigate quality issues and customer complaints with root-cause analysis.
• Communicate quality system requirements and support training.
• Support audits and CAPA activities.

Skills

Quality Assurance

Documentation

Regulatory awareness

Cross-functional collaboration

Attention to detail

Education

Life Sciences/Pharmacy/Chemistry degree

Tools

Microsoft Office

Job description

Clinigen Group is seeking a proactive Quality Release Specialist to join our Quality and Warehouse teams in the UK. You will help maintain GMP and GDP compliance and support the QMS, ensuring product quality and patient safety across activities.

You will collaborate with cross‑functional partners, investigators and regulators to review quality records, author documentation, and drive continuous improvement within a fast‑paced, global pharmaceutical environment.