Quality Assurance Officer – Pharmaceuticals

JR United Kingdom; Portsmouth; On-site; GBP 34,000 - 42,000; Full time

Job summary

A leading biopharmaceutical company is seeking an experienced Quality Assurance Officer for a 12-month contract in Portsmouth. The role involves ensuring compliance with regulations, managing quality systems, and conducting internal audits. With a base salary of up to £42,000 and an additional shift allowance, this is an excellent opportunity to impact a reputable organization.

Qualifications

• Experience in Quality Assurance within pharmaceuticals/biopharmaceuticals.
• Strong understanding of GMP.
• Experience in clean room or manufacturing environments is advantageous.

Responsibilities

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

Skills

Communication

Teamwork

Quality Management

GMP

Education

BSc or MSc in a relevant scientific discipline

Tools

Quality Management System

Job description

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Quality Assurance Officer – Pharmaceuticals, Portsmouth, Hampshire

Client: CY Partners

Location: Portsmouth, Hampshire, 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 seeking an experienced Quality Assurance Officer to join their growing team. You will ensure all Quality Assurance activities meet the highest standards, complying with all relevant 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, and agreeing on appropriate actions.
• Acting as the primary QA contact across the site.
• Providing guidance on deviations and quality incidents.
• Conducting quality investigations, internal audits, and supporting regulatory audits.

Candidate requirements:

• Experience in Quality Assurance within pharmaceuticals / biopharmaceuticals.
• Proficiency with quality documentation and QMS.
• Strong understanding of GMP.
• Experience in clean room or manufacturing environments is advantageous.
• Excellent 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 make a significant impact in a reputable Biopharmaceutical company.

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

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

Applicants must prove legal right to work in the UK. CY Partners Recruitment Ltd is an Employment Business/Agency.