Quality Systems Manager

Quality Systems Manager

Burton upon Trent Site-Based Permanent

Talentmark is delighted to be recruiting for an established pharmaceutical manufacturer seeking an experienced Quality Systems Manager to lead the Quality Systems & Compliance function within its aseptic compounding unit.

This is a key leadership role with responsibility for the site Quality Management System (QMS) ensuring robust processes strong compliance and a culture of continuous improvement. Youll play a vital role in reducing variation and ensuring the site remains GMP/GDP compliant and audit-ready ultimately supporting safe patient outcomes.

The Role

Youll take ownership of the Quality Management System and provide oversight across key quality processes working closely with operational and quality teams.

Responsibilities:

• Owning and maintaining the QMS ensuring it remains effective and compliant.
• Managing document and data control including review and approval of controlled documentation and quality records.
• Monitoring and reporting quality KPIs trends and performance to the Aseptic Compounding Management Team.
• Overseeing CAPAs complaints deviations nonconformances and quality risk management.
• Leading internal audits and coordinating responses to external regulatory and customer audits.
• Driving effective investigations and ensuring corrective actions are delivered promptly.
• Identifying opportunities to improve processes reduce variation and strengthen quality performance.

Your Background:

Were looking for a quality professional with strong Quality Systems knowledge who thrives in a regulated pharmaceutical environment and enjoys solving problems and improving processes.

Essential:

• Degree-level qualification in a relevant Life Sciences discipline.
• Strong knowledge of Quality Management Systems and processes.
• Working knowledge of EU/UK GMP.
• Experience across Document Control Internal Audit CAPA Nonconformance and Complaints.
• Strong investigation and problem-solving skills with experience using tools such as 8D 5 Whys Cause & Effect or Gemba
• Experience within pharmaceuticals medical devices biotechnology microbiology regulated industries.

This is an excellent opportunity to take a leading role in shaping quality culture and compliance within an aseptic compounding environment with the opportunity to make improvements that directly support patient safety and clinical outcomes.

Benefits:

The organisation offers a competitive salary and comprehensive benefits package including:

• Private Healthcare cover.
• Company Pension Scheme.
• Life Assurance.
• Gym Discount.
• Access to Wellness platforms.
• Yearly Pay Reviews.

Apply:

It is essential that applicants hold entitlement to work in the UK. Please quote job reference 71440 in all correspondence.