Quality Assurance Officer – Pharmaceuticals

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

Job summary

A leading biopharmaceutical company seeks a Quality Assurance Officer in Dartford. This role involves ensuring compliance with quality standards, managing documentation, and conducting quality investigations. Ideal candidates will have extensive QA experience in pharmaceuticals, a relevant degree, and excellent communication skills.

Qualifications

• Experience in Quality Assurance within pharmaceuticals or biopharmaceuticals.
• Strong understanding of GMP regulations.
• Experience in a clean room or manufacturing environment is advantageous.

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

Quality Assurance

Documentation Management

Communication

Teamwork

Education

BSc or MSc in a relevant scientific discipline

Job description

Quality Assurance Officer – Pharmaceuticals

Location: Dartford, 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:

Role: Quality Assurance Officer – Pharmaceuticals

Location: North London

Contract: 12 Months

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

Are you an experienced quality assurance professional within Pharmaceuticals/Biopharmaceuticals? Are you seeking a challenging 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 high standards and comply with regulations and best practices.

This position 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 documents, including Batch Manufacturing Records.
3. Review and respond to quality records such as deviations, complaints, and change controls.
4. Serve as the primary QA contact across the site.
5. Provide guidance on deviations and quality incidents.
6. Conduct quality investigations, internal audits, and support regulatory audits.

Candidate requirements:

1. Experience in Quality Assurance within pharmaceuticals or biopharmaceuticals.
2. Experience with quality documentation and management systems (QMS).
3. Strong understanding of GMP regulations.
4. Experience in a clean room or manufacturing environment 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 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, GxP, Regulatory Compliance, Deviation, CAPA, GLP, GDP, Pharmaceutical, Biopharmaceutical, North London"

The employer states that all applicants must be legally entitled to work in the UK. CY Partners Recruitment Ltd is an employment agency.