Our client provides the most comprehensive range of services extending from research through pharmaceutical and clinical development to commercialisation of product. An exciting opportunity has arisen for a Quality Compliance Manager to join their team on a permanent basis.

As a key member of the Quality Assurance team, the role of the Quality Compliance Manager is to ensure that all requirements of the Quality Management System (QMS) are managed on a day to day basis. This role will also be fundamental in driving continual improvement in line with customer expectations and regulatory demands.

We are looking for a highly motivated and organised individual who can work successfully within a team environment.

Responsibilities:
- Manage the day to day administration of all Quality Management System elements in line with the Quality Policy.

- Manage a number of structured teams to effectively and efficiently support the business on QMS related matters.

- Act as a 'Subject Matter Expert' on the Quality Management System and become a primary point of contact for other departments and customers as required.

- Manage the workload of structured teams and actively manage the performance and development of staff.

- Ensure that all work is allocated and performed to a high standard and fitting with the time expectations of internal and external customers.

- Host / Co host customer / regulatory audits as required.

- Manage the audit schedules in line with risk management principles and participate in audits as required.

- Provide QA input into Risk Management programmes.

- Stay current with legislation, guidelines and other expectations of the pharmaceutical industry especially in relation to GMP and Quality Management.

- Identify and implement continuous improvement within the department and wider business.

- Assist in the implementation of key business projects.

- Communicate effectively with other employees and participate with them in planning and problem solving activities, as required.

- React to system trending (e.g. deviations, complaints, OOS) to ensure ongoing quality performance.

- Ensure documentation is generated and completed in accordance with the principles of GMP and internal SOPs.


What we are looking for:
- Significant experience working within an established Quality System within a Pharmaceutical or Medical Devices Industry.

- Experience of all quality system aspects including: Deviation management, CAPA, complaint handling, auditing, change management, supplier qualification

- Experience of customer and / or regulatory audits (FDA, MHRA, EMEA etc).

- Significant experience of managing people.

- Good knowledge of the legal requirements, rules and guidance covering the manufacture of pharmaceutical products in Europe

- Experience in the manufacture of pharmaceutical products.


This role will involve some travel so candidates must consider this before applying.


To apply for this position, candidates must be eligible to live and work in the UK
Matchtech Group UK Limited is acting as an Employment Agency in relation to this vacancy.Apply now