Quality Assurance Officer – Pharmaceuticals

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

Job summary

A leading biopharmaceutical firm in Chesterfield is seeking a Quality Assurance Officer to ensure compliance with GxP standards and manage quality documentation. The role offers a competitive salary package including an £8,000 shift allowance. The company is dedicated to providing high-quality biological materials and values team collaboration and communication.

Qualifications

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

Responsibilities

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

Skills

Compliance with GxP standards

Quality Management System management

Quality documentation familiarity

Excellent communication

Teamwork skills

Education

BSc or MSc in a relevant scientific discipline

Job description

Quality Assurance Officer – Pharmaceuticals

Location: Chesterfield, United Kingdom

Client: CY Partners

Job Category: Other

Contract Duration: 12 months

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

EU work permit required: Yes

Posted: 04.06.2025

Expiry Date: 19.07.2025

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? CY Partners is looking for an experienced Quality Assurance Officer to join a leading company that delivers high-quality biological materials. In this role, you will ensure all QA activities meet the highest standards, comply with regulations, and follow best practices.

This position is based in North London and is offered on a shift basis.

Key Responsibilities:

• Ensure compliance with GxP, Quality, and Health & Safety standards within the Pharmaceutical QA team.
• Manage the Quality Management System and review quality documents, including Batch Manufacturing Records.
• Handle deviations, complaints, and change controls, and agree on appropriate actions.
• Serve as the primary QA contact across the site.
• Provide guidance on deviations and quality incidents.
• Conduct quality investigations, internal audits, and support regulatory audits.

Qualifications and Experience:

• Experience in Quality Assurance within pharmaceuticals or biopharmaceuticals.
• Familiarity with quality documentation and management systems (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 for a passionate QA professional to make an impact in a reputable biopharmaceutical company. To apply, please submit your application online or contact Katie-May Kress at CY Partners for more information.