Quality Assurance Officer – Pharmaceuticals

JR United Kingdom; Coventry; On-site; GBP 35,000 - 42,000; Full time

Job summary

A leading biopharmaceutical company in North London is seeking a Quality Assurance Officer to ensure compliance with industry standards. The role involves managing quality systems, conducting audits, and providing guidance on quality aspects, ideal for those with a relevant scientific background. A competitive salary and shift allowance are on offer, making this an excellent opportunity for passionate QA professionals.

Qualifications

• Experience in Quality Assurance within pharmaceuticals or biopharmaceuticals.
• Understanding of Good Manufacturing Practice (GMP).
• Experience with quality documentation and management systems.

Responsibilities

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

Skills

Communication

Teamwork

Education

BSc or MSc in a relevant scientific discipline

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 growing team. You will ensure all Quality Assurance activities meet high standards, regulations, and best practices.

This role operates on a shift basis.

Key responsibilities:

1. Ensuring compliance with GxP, Quality, and Health & Safety standards within the Pharmaceutical QA team.
2. Managing the Quality Management System and reviewing Batch Manufacturing Records.
3. Responding to quality records such as deviations, complaints, and control changes.
4. Serving as the primary QA contact across the site.
5. Providing guidance on deviations and quality incidents.
6. Conducting quality investigations, internal audits, and supporting on-site regulatory audits.

Candidate requirements:

1. Experience in Quality Assurance within pharmaceuticals or biopharmaceuticals.
2. Experience with quality documentation and quality management systems (QMS).
3. Understanding of Good Manufacturing Practice (GMP).
4. Experience in a clean room or manufacturing environment is advantageous.
5. Strong communication and teamwork skills.
6. BSc or MSc in a relevant scientific discipline or equivalent experience.
7. Full UK Driving Licence and access to a vehicle.

This is an excellent opportunity for a passionate QA professional to make an 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, QA Associate, Quality Investigations, GMP, GLP, GDP, Pharmaceutical, Biopharmaceutical, North London"

Note: All applicants must prove legal entitlement to work in the UK. CY Partners Recruitment Ltd is an Employment Business/Agency.