Quality Assurance Officer – Pharmaceuticals

JR United Kingdom; Leeds; On-site; GBP 42,000 - 49,000; Full time

Job summary

A leading biopharmaceutical company is seeking an experienced Quality Assurance Officer for a 12-month contract in Leeds. The role focuses on ensuring compliance with regulations and managing the Quality Management System. Strong expertise in QA within pharmaceuticals is required, along with a relevant scientific degree. This opportunity also includes a competitive salary and additional shift allowances.

Qualifications

• Experience in Quality Assurance within pharmaceuticals / biopharmaceuticals.
• Knowledge of quality documentation and QMS.
• Understanding of GMP regulations.

Responsibilities

• Ensure compliance with GxP, Quality, and Health & Safety standards.
• Manage the Quality Management System and review quality documents.
• Conduct quality investigations and internal audits.

Skills

Quality Assurance

Communication

Teamwork

Education

BSc or MSc in a relevant scientific discipline

Job description

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Quality Assurance Officer – Pharmaceuticals, Leeds, West Yorkshire

Client: CY Partners

Location: Leeds, West Yorkshire, 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?

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 high standards, regulations, and best practices.

This role is shift-based.

Key responsibilities:

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

Requirements:

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

This is an excellent opportunity to impact a reputable biopharmaceutical company.

Apply online or contact Katie-May Kress at CY Partners for more info.

Keywords: "Quality Assurance Officer, QA, QA Associate, Quality Investigations, Manufacturing, QMS, GXP, Regulatory Compliance, Deviation, CAPA, GMP, GLP, GDP, Pharmaceutical, Biopharmaceutical, London, North London"

The recruiter states all applicants must prove legal right to work in the UK. CY Partners Recruitment Ltd is an Employment Business/Agency.