Quality Assurance Officer – Pharmaceuticals

JR United Kingdom; Woking; On-site; GBP 42,000 - 50,000; Full time

Job summary

A leading biopharmaceutical company is seeking a Quality Assurance Officer in Woking for a 12-month contract. This role involves ensuring compliance with quality standards and managing quality systems. Candidates should have relevant QA experience, strong communication skills, and a life sciences degree. This shift-based role offers a competitive salary and an additional shift allowance.

Qualifications

• Experience in QA within pharmaceuticals or biopharmaceuticals.
• Knowledge of quality documentation and QMS.
• Understanding of GMP.

Responsibilities

• Ensure compliance with GxP, Quality, and Health & Safety standards.
• Manage the Quality Management System and review Batch Manufacturing Records.
• Serve as the primary QA contact across the site.

Skills

Quality Assurance

Communication

Teamwork

Education

BSc or MSc in a relevant scientific discipline

Job description

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Quality Assurance Officer – Pharmaceuticals, Woking

Client: CY Partners

Location: Woking, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views: 3

Posted: 04.06.2025

Expiry Date: 19.07.2025

Job Description:

Quality Assurance Officer – Pharmaceuticals

Based in North London

12 Month Contract

Salary up to £42,000 + £8,000 shift allowance

Are you a quality assurance professional with experience in Pharmaceuticals / Biopharmaceuticals?

Are you seeking a challenging and rewarding role in the pharmaceutical industry?

My client, a leader in delivering high-quality, processed biological materials, is looking for an experienced Quality Assurance Officer to join their team. You will ensure all QA activities meet the highest standards, regulations, and best practices.

This role is shift-based.

Key responsibilities:

• Ensure compliance with GxP, Quality, and Health & Safety standards within the Pharmaceutical QA team.
• Manage the Quality Management System and review Batch Manufacturing Records.
• Handle quality records, deviations, complaints, and control changes.
• Serve as the primary QA contact across the site.
• Guide internal departments on deviations and quality incidents.
• Conduct investigations, internal audits, and support regulatory audits.

Requirements:

• Experience in QA within pharmaceuticals / biopharmaceuticals.
• Knowledge of quality documentation and QMS.
• Understanding of GMP.
• Experience in a clean room or manufacturing environment is advantageous.
• Strong communication and teamwork skills.
• BSc or MSc in a relevant scientific discipline or equivalent.
• Full UK Driving Licence and access to a vehicle.

This is an excellent opportunity for a passionate QA professional to impact a reputable biopharmaceutical company.

Please apply online or contact Katie-May Kress at CY Partners for more information.

Keywords include: QA, QMS, GMP, Biopharmaceutical, North London, etc.

Applicants must be legally entitled to work in the UK. CY Partners Recruitment Ltd is an Employment Business/Agency.