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Quality Systems Manager

Job in Burton upon Trent, Staffordshire, DE13 0AD, England, UK
Listing for: Talentmark
Full Time position
Listed on 2026-10-09
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 70000 - 90000 GBP Yearly GBP 70000.00 90000.00 YEAR
Job Description & How to Apply Below
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. You'll 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

You’ll 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:
  • 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 with in 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:
  • Private Healthcare cover.
  • Company Pension Scheme.
  • Life Assurance.
  • Gym Discount.
  • Access to Wellness platforms.
  • Yearly Pay Reviews.
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