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Quality Manager

Location: NETHERLANDS Salary: Salary Negotiable
Sector: Scientific Job Type: Permanent
Shift Type: DAYS ONLY Applications: N/A
Posted: 30 days ago Reference: 3080907
Role: Quality Manager
Duration: Permanent
Sector: Pharmaceuticals
Location: The Netherlands


A leading pharmaceutical organisation specialising in facial aesthetics and dermatology are currently seeking a skilled Quality Manager to work within their Manufacturing facility in the Netherlands. This position would suit applications from individuals with experience managing a successful Quality Assurance team, and strong working knowledge of ISO, US FDA and GMP regulations.

A competitive salary and bonus scheme will be offered to the successful candidate.


Role responsibilities:

Ensure all production activities are compliant with documented (QMS) procedures and in accordance with applicable standards (e.g. ISO 13485)

Take a pivotal role in leading the development of the quality management system, writing SOPs and training staff in all aspect of the QMS/SOPs as required

Assist in improving overall quality, efficiency and effectiveness of the operations within the QA and Production departments by means of proactive initiatives

Support the departments RDT and Operations by reporting and trending data relevant to production, QC and projects, both proactively and periodically to support management reviews

Manage and maintain the internal audit program as well as the schedule of approved supplier audits

Deputise for the Quality Director when required, and act as the Management Representative in accordance with the requirements of ISO 13485, also performing final product release and thus ensuring compliance with defined specifications





Person Specification:

Able to communicate both written and verbal in both English and Dutch

Scientific degree (ideally pharmacy, pharmaceutical sciences, chemistry or related)

Experience of leading a successful Quality Assurance team

Experience of working with a Quality Management System to ISO13485 (preferably in a medical device production environment)

Knowledge of ISO, US FDA and GMP regulations

Preferably a qualified lead auditor to ISO 13485 or ISO9001



If this position is of interest, please submit your CV and covering letter via the link, and we will look forward to receiving your application.

If you require further information please contact Katie Roddis on 01223 463300 or at katie.roddis@reedglobal.com


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