Quality Assurance Officer – Pharmaceuticals

JR United Kingdom; Hounslow; On-site; GBP 34,000 - 42,000; Full time

Job summary

A leading biopharmaceutical company is seeking a Quality Assurance Officer in South West London. This role offers a competitive salary of up to £42,000 with an £8,000 shift allowance, focusing on ensuring compliance with QA standards and regulations. The ideal candidate will have a scientific background and experience in QA within the pharmaceuticals industry.

Qualifications

• Experience in QA within pharmaceuticals or biopharmaceuticals required.
• Knowledge of quality documentation and Quality Management Systems (QMS).
• Understanding of GMP standards.

Responsibilities

• Ensuring compliance with GxP, Quality, and Health & Safety standards.
• Managing the Quality Management System and reviewing Batch Manufacturing Records.
• Conducting quality investigations and audits, supporting regulatory inspections.

Skills

Strong communication

Teamwork

Education

BSc or MSc in a relevant scientific discipline

Job description

Quality Assurance Officer – Pharmaceuticals

Location: South West London, United Kingdom

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?

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 the highest standards and comply with regulations.

This role operates 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.
• Addressing quality records issues such as deviations, complaints, and control changes.
• Serving as the primary QA contact across the site.
• Providing guidance on deviations and quality incidents.
• Conducting quality investigations and audits, and supporting regulatory inspections.

Requirements:

• Experience in QA within pharmaceuticals or biopharmaceuticals.
• Knowledge of quality documentation and QMS.
• Understanding of GMP standards.
• 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 license and access to a vehicle.

This is a great opportunity for a passionate QA professional to impact a reputable biopharmaceutical company. Please apply online or contact Katie-May Kress at CY Partners for more information.

Keywords include: "Quality Assurance Officer, QA, QMS, GMP, Regulatory Compliance, Deviation, CAPA, Pharmaceutical, Biopharmaceutical, London, North London".

The position is active, and applicants must prove legal entitlement to work in the UK.