Quality Assurance Officer – Pharmaceuticals

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

Job summary

Une entreprise biopharmaceutique de premier plan recherche un Quality Assurance Officer qualifié pour rejoindre son équipe à Stockport. En tant que professionnel en assurance qualité, vous serez responsable d'assurer le respect des normes GxP et de gérer le système de qualité. Vous aurez ainsi l'opportunité d'influencer directement les opérations au sein de cette société réputée.

Qualifications

• Expérience en assurance qualité dans les secteurs pharmaceutique ou biopharmaceutique.
• Compréhension des normes GMP et documentation qualité.
• Permis de conduire UK requis.

Responsibilities

• Assurer la conformité avec les normes GxP, qualité et santé & sécurité.
• Gérer le système de gestion de la qualité et examiner les documents de fabrication.
• Mener des enquêtes de qualité et soutenir les audits réglementaires.

Skills

Quality Assurance

Communication

Teamwork

Education

BSc or MSc in a relevant scientific discipline

Job description

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Quality Assurance Officer – Pharmaceuticals, Stockport

Client: CY Partners

Location: Stockport, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views: 3

Posted: 04.06.2025

Expiry Date: 19.07.2025

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 / Biopharmaceuticals?

Are you seeking a challenging and rewarding 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 growing team. You will ensure all QA activities meet the highest standards, complying with regulations and best practices.

This role is on a shift basis.

Key responsibilities include:

• Ensuring compliance with GxP, Quality, and Health & Safety standards within the Pharmaceutical QA team.
• Managing the Quality Management System and reviewing Batch Manufacturing Records.
• Handling deviations, complaints, and control changes, and approving appropriate actions.
• Serving as the primary QA contact across the site.
• Providing guidance on deviations and quality incidents.
• Conducting quality investigations, internal audits, and supporting regulatory audits.

Requirements:

• Experience in Quality Assurance within pharmaceuticals or biopharmaceuticals.
• Familiarity with quality documentation and QMS.
• Understanding of GMP standards.
• Experience in a clean room or manufacturing environment 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 an excellent 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: "Quality Assurance Officer, QA, QA Associate, Quality Assurance, Quality Investigations, Quality, Manufacturing, QMS, GXP, Regulatory Compliance, Deviation, CAPA, GMP, GLP, GDP, Pharmaceutical, Biopharmaceutical, London, North London"

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