Quality Assurance Officer – Pharmaceuticals

JR United Kingdom; Stoke-on-Trent; On-site; GBP 34,000 - 42,000; Full time

Job summary

A reputable biopharmaceutical company is seeking a Quality Assurance Officer – Pharmaceuticals for a 12-month contract in Stoke-on-Trent. The successful applicant will ensure compliance with quality standards and manage QA systems, offering a competitive salary along with a shift allowance.

Qualifications

• Experience in QA within pharmaceuticals or biopharmaceuticals.
• Knowledge of quality documentation and 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 supporting regulatory audits.

Skills

Communication

Teamwork

Education

BSc or MSc in a relevant scientific discipline

Job description

Quality Assurance Officer – Pharmaceuticals

Location: Stoke-on-Trent, 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:

We are seeking an experienced Quality Assurance Officer – Pharmaceuticals based in North London for a 12-month contract with a salary up to £42,000 plus an £8,000 shift allowance. The successful candidate will play a key role in ensuring all QA activities meet high standards, complying with all relevant regulations.

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 acting as the primary QA contact on-site.
• Providing guidance on deviations and quality incidents.
• Conducting quality investigations, internal audits, and supporting regulatory audits.

Candidate requirements:

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

This role offers an excellent opportunity to contribute to a reputable biopharmaceutical company. To apply, please submit your application online or contact Katie-May Kress at CY Partners for more information.