Senior Quality Assurance Associate

Are you a QA professional with a passion for GMP compliance and continuous improvement in a cutting-edge biotechnology environment?

R&D Partners is seeking a Senior Quality Assurance Associate to join a leading biotechnology company in London. This role focuses on providing QA oversight across manufacturing and operational functions, ensuring compliance with GMP standards, and driving continuous improvement initiatives.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Provide QA oversight across manufacturing and operational functions.
• Manage and continuously improve the Quality Management System (QMS).
• Review and approve GMP documentation, including SOPs, quality processes, and training materials.
• Support batch record review and GMP product release activities.
• Lead quality investigations, including deviations, CAPAs, change controls, risk assessments, and OOS activities.
• Perform internal audits and support customer and regulatory inspections.
• Deliver compliance training and mentor QA team members.
• Drive continuous improvement initiatives and promote a quality culture across the site.

Key Skills and Requirements:

• Minimum of 5 years of experience in a sterile GMP manufacturing environment.
• Strong background in QA and compliance.
• Hands-on experience with regulatory inspections and audits.
• Excellent knowledge of Quality Systems and GMP requirements.

For more information, please contact Henry LeLacheur.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

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