Quality Assurance Officer – Pharmaceuticals

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

Job summary

A leading biopharmaceutical company is seeking an experienced Quality Assurance Officer in Bolton. The successful candidate will manage the Quality Management System, ensure compliance with industry standards, and guide teams on quality incidents. This role offers a competitive salary package including a shift allowance for dedicated professionals.

Qualifications

• Experience in QA within pharmaceuticals or biopharmaceuticals.
• Knowledge of quality documentation and QMS.
• Experience in clean room or manufacturing environments is advantageous.

Responsibilities

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

Skills

Quality Assurance

GMP Principles

Communication

Teamwork

Education

BSc or MSc in relevant scientific discipline

Job description

Quality Assurance Officer – Pharmaceuticals

Location: Bolton, Greater Manchester, United Kingdom

Client: CY Partners

Job Category: Other

EU work permit required: Yes

Job Views: 3

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 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 QA activities meet high standards and comply with regulations and best practices.

This role is based in Bolton and is offered on a shift basis with a salary up to £42,000 plus an £8,000 shift allowance.

Key Responsibilities:

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

Qualifications and Skills:

• Experience in QA within pharmaceuticals or biopharmaceuticals.
• Knowledge of quality documentation and QMS.
• Understanding of GMP principles.
• Experience in clean room or manufacturing environments is advantageous.
• Strong 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 a great opportunity to make an impact in a reputable biopharmaceutical company. Please apply online or contact Katie-May Kress at CY Partners for more details.