Quality Assurance Officer – Pharmaceuticals

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

Job summary

A leading biopharmaceutical company in Bristol seeks a Quality Assurance Officer to ensure compliance with quality standards and manage QA activities. Candidates should have a solid background in pharmaceuticals or biopharmaceuticals, as well as relevant qualifications. This is a rewarding role offering a salary of up to £42,000 with an additional shift allowance.

Qualifications

• Experience in Quality Assurance within pharmaceuticals or biopharmaceuticals.
• Experience with quality documentation and QMS.
• Full UK Driving Licence and access to a vehicle.

Responsibilities

• Ensuring compliance with GxP, Quality, and Health & Safety standards.
• Managing the Quality Management System and reviewing Batch Manufacturing Records.
• Conducting quality investigations and supporting regulatory audits.

Skills

Quality Assurance

GMP

GxP

Deviations

Regulatory Compliance

Teamwork

Communication

Education

BSc or MSc in a relevant scientific field

Job description

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Quality Assurance Officer – Pharmaceuticals, Bristol

Client: CY Partners

Location: Bristol, 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 Quality Assurance activities meet the highest standards, regulations, and best practices.

This role is shift-based.

Key responsibilities include:

• Ensuring compliance with GxP, Quality, and Health & Safety standards within the Pharmaceutical QA team.
• Managing the Quality Management System and reviewing Batch Manufacturing Records.
• Handling deviations, complaints, and control changes by reviewing and agreeing on actions.
• Serving as the primary QA contact across the site.
• Providing guidance on deviations and quality incidents.
• Conducting quality investigations, internal audits, and supporting regulatory audits.

Requirements:

• Experience in Quality Assurance within pharmaceuticals or biopharmaceuticals.
• Experience with quality documentation and QMS.
• Understanding of GMP.
• Experience in clean rooms or manufacturing environments is advantageous.
• Strong communication and teamwork skills.
• BSc or MSc in a relevant scientific field or equivalent experience.
• 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.

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

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

The employer states that applicants must prove they are legally entitled to work in the UK.