Quality Assurance Officer – Pharmaceuticals

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

Job summary

A leading biopharmaceutical company is seeking a Quality Assurance Officer to ensure compliance and manage quality documents within the industry. The role offers an excellent career opportunity for a QA professional, requiring a BSc or MSc and experience in pharmaceuticals. With a salary of up to £42,000 plus a shift allowance, it's an enticing position for those seeking growth in a reputable firm in North London.

Qualifications

• Experience in Quality Assurance within pharmaceuticals or biopharmaceuticals.
• Familiarity with quality documentation and QMS.
• Experience in clean rooms or manufacturing environments 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

Knowledge of GMP

Excellent communication

Teamwork skills

Education

BSc or MSc in relevant scientific field

Job description

Quality Assurance Officer – Pharmaceuticals

Location: North London

Contract: 12 months

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

Are you a quality assurance professional with experience in Pharmaceuticals or 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, comply with regulations, and follow 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. Address deviations, complaints, and control changes through appropriate actions.
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. Familiarity with quality documentation and QMS.
3. Strong knowledge of GMP.
4. Experience in clean rooms or manufacturing environments is advantageous.
5. Excellent communication and teamwork skills.
6. BSc or MSc in a relevant scientific field or equivalent experience.
7. Full UK Driving Licence and access to a vehicle.

This is an excellent opportunity for a passionate QA professional to contribute to a reputable biopharmaceutical company.

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, London, North London"

The employer requires all applicants to prove their legal right to work in the UK. CY Partners Recruitment Ltd operates as an Employment Business/Agency.