Quality Assurance Officer – Pharmaceuticals

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

Job summary

A leading biopharmaceutical company is seeking a Quality Assurance Officer in North London. This role involved ensuring compliance with quality standards and managing documentation within the Pharma QA team. The ideal candidate will have significant QA experience in pharmaceuticals, relevant qualifications, and excellent teamwork abilities. This opportunity offers a competitive salary along with a shift allowance, contributing to a rewarding career in an impactful environment.

Qualifications

• Experience in pharmaceuticals or biopharmaceuticals required.
• Strong understanding of GMP standards essential.
• Experience in clean room or manufacturing environment is advantageous.

Responsibilities

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

Skills

Experience in Quality Assurance

Communication

Teamwork

Education

BSc or MSc in a relevant scientific discipline

Job description

Quality Assurance Officer – Pharmaceuticals

Based in North London

12 Month Contract

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

Are you a quality assurance professional with experience in Pharmaceuticals or Biopharmaceuticals?

Seeking a challenging and rewarding 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 growing team. You will ensure all QA activities meet the highest standards, regulations, and best practices.

This role operates 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.
• Review and approve actions related to quality records such as deviations, complaints, and control changes.
• Serve as the primary QA contact on-site.
• Guide and advise internal departments on deviations and quality incidents.
• Conduct quality investigations, internal audits, and support regulatory audits.

Candidate requirements:

• Experience in Quality Assurance within pharmaceuticals or biopharmaceuticals.
• Experience with quality documentation and Quality Management Systems (QMS).
• Strong understanding of GMP standards.
• Experience in a clean room or manufacturing environment 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 a significant impact in a reputable biopharmaceutical company.

Please apply online or contact Katie-May Kress at CY Partners for more information.

Keywords: "Quality Assurance Officer, QA, QA Associate, Quality Investigations, Quality, Manufacturing, QMS, GXP, Regulatory Compliance, Deviation, CAPA, GMP, GLP, GDP, Pharmaceutical, Biopharmaceutical, London, North London"

The recruiter states that all applicants must prove their legal right to work in the UK. CY Partners Recruitment Ltd is an Employment Business/Agency.