Quality Systems and Compliance Manager

Walker Cole International Ltd; East Midlands; Presencial; GBP 60 000 - 75 000; Tempo integral

Resumo da oferta

Walker Cole International is seeking a Quality Systems and Compliance Manager to join a well-established healthcare and life sciences organisation in the East Midlands. You will own the Quality Management System, ensuring EU/UK GMP and GDP compliance and audit readiness across the site.

You will lead document control, quality data, KPIs, risk management and audits, while developing a team of three in a full-time, site-based role. Strong QMS knowledge and leadership are essential.

Qualificações

• Degree in Life Sciences or equivalent with quality focus.
• Experience in regulated industries (pharma/medical device).
• Strong understanding of QMS and EU/UK GMP knowledge.

Responsabilidades

• Own the Quality Management System and ensure GMP/GDP compliance.
• Lead internal audits and coordinate responses to external audits.
• Drive CAPA, deviations and complaint investigations with timely actions.
• Coordinate risk management and data-driven quality improvements.
• Develop and mentor a team of three; drive continuous improvement.

Conhecimentos

Quality management

QMS knowledge

Team leadership

Regulatory knowledge

Audit coordination

CAPA handling

Documentation control

Formação académica

Degree in Life Sciences

Descrição da oferta de emprego

Walker Cole International is supporting a well-established healthcare and life sciences organisation in the search for a Quality Systems and Compliance Manager to join their team, based in the East Midlands.

This is an excellent opportunity to lead the Quality Systems and Compliance function, supplying medicines that directly support patient care. You will own the Quality Management System, ensuring the site meets GMP and GDP requirements and remains audit-ready at all times. The role offers broad leadership exposure across document control, quality data and KPIs, risk management and internal and external audits.

This role would suit an experienced quality professional with strong QMS knowledge and people management experience, who is looking to lead and develop a team of three in a full-time, site-based role.

You will be responsible for:

• Owning the Quality Management System and ensuring compliance with EU/UK GMP and GDP requirements.
• Ensuring all controlled documentation is current, accurate and accessible, and reviewing and approving new and updated procedures.
• Ensuring quality records are complete, legible and compliant with good documentation practice.
• Tracking, trending and monitoring quality data, including CAPAs, complaints and deviations, to ensure timely completion..
• Leading internal audits and coordinating responses to external, regulatory and customer audits.
• Driving investigation of audit findings and ensuring corrective actions are delivered promptly and effectively.
• Championing risk identification and management across the unit.
• Managing and developing a team of three, and driving continuous improvement by reducing waste and variation.

The successful candidate will have:

• A degree in a relevant Life Sciences discipline, or equivalent experience in quality facilitation, process improvement or quality data analysis.
• Experience within pharmaceuticals, medical devices, biotechnology or a similar regulated industry.
• Strong knowledge of Quality System processes and a working knowledge of EU/UK GMP.
• Experience in document control, internal audit, CAPA, nonconformance and complaints processes.
• Experience with problem-solving tools such as 8D, Gemba, 5 Whys and cause and effect analysis.
• Strong communication, coordination and people management skills, with excellent attention to detail and organisational ability.

Quality Systems Manager | Compliance Manager | Quality Assurance | QA | QMS | GMP | GDP | EU GMP | UK GMP | Aseptic | Document Control | Internal Audit | CAPA | Deviations | Complaints | Risk Management | Continuous Improvement | Pharmaceutical