Quality Assurance Officer – Pharmaceuticals

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

Job summary

A leading biopharmaceutical company seeks a Quality Assurance Officer to ensure compliance and high standards in a 12-month role. The position involves managing quality documentation, guiding teams on QA, and conducting audits. Ideal for candidates with a scientific background and QA experience in pharmaceuticals.

Qualifications

• Experience in Quality Assurance within pharmaceuticals or biopharmaceuticals.
• Proficiency with quality documentation and QMS.
• Strong understanding of GMP.

Responsibilities

• Ensure compliance with GxP, Quality, and Health & Safety standards.
• Manage the Quality Management System and review documentation.
• Guide internal departments on deviations and quality incidents.

Skills

Quality Assurance

GMP

Communication

Teamwork

Education

BSc or MSc in relevant scientific discipline

Job description

Quality Assurance Officer – Pharmaceuticals

Location: North London

Contract: 12 Months

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

Job Description:

Are you a quality assurance professional with experience in Pharmaceuticals or Biopharmaceuticals? Are you seeking a challenging and rewarding role in the pharmaceutical industry?

Our 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, complying with regulations and best practices.

This role operates on a shift basis.

Key Responsibilities:

1. Ensure compliance with GxP, Quality, and Health & Safety standards within the Pharmaceutical QA team.
2. Manage the Quality Management System and review quality documentation, including Batch Manufacturing Records.
3. Review quality records such as deviations, complaints, and control changes, and coordinate appropriate responses.
4. Serve as the primary QA contact across the site.
5. Guide internal departments on deviations and quality incidents.
6. Conduct quality investigations, internal audits, and support regulatory audits.

Qualifications and Experience:

1. Experience in Quality Assurance within pharmaceuticals or biopharmaceuticals.
2. Proficiency with quality documentation and QMS.
3. Strong understanding of GMP.
4. Experience in clean room or manufacturing environments is advantageous.
5. Excellent 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 a great opportunity for a passionate QA professional to impact a reputable biopharmaceutical company.

Interested candidates should apply online or contact Katie-May Kress at CY Partners for more information.

Keywords include: "Quality Assurance Officer, QA, Quality Management System, GMP, Regulatory Compliance, Deviation, CAPA, Pharmaceutical, Biopharmaceutical, North London".

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