This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies. Find out more here.

Close Message for pharmaceutical industry jobs
NonStop Recruitment is dedicated to putting job seekers looking for pharmaceutical industry jobs in touch with recruiters and employers.

Similar jobs you may be interested in:

Senior Regulatory Affairs Manager (m/w)
Dental Product Specialist - West Switzerland - NEW!
Regulatory Affairs Manager - Clinical Development - Scotland
Scotland (Central)
Associate Director of Regulatory Affairs - Midsize consultancy
Regulatory Publishing Associate
South East

To receive a FREE weekly email alert of all the latest pharmaceutical industry jobs added to our database enter your email address below.

Submit | Tell me more...

Sister site:
Our sister site
Job Details
This job has expired. Click here to view similar jobs.

Senior Quality Engineer - Medical Devices - Netherlands

Business Type: Healthcare Company, Medical Devices Company, Contract Manufacturing
Job Type: Medical Devices, Quality Assurance - Control, Audit, Regulatory Affairs, Compliance
Job Level: Management
Position: Full Time
Salary: benefits
Location: Netherlands
Reference: AB-SQEH-1
Closing Date: 18/08/12

Our client is a leading contract developer and manufacturer, producing quality medical and pharmaceutical components, as well as finished devices. With offices in a Europe, Scandinavia and the USA, they are a growing organisation and in need of a Senior Quality Engineer to bolster the Dutch operations, taking responsibility for maintenance and continuous improvement of the plant quality system.

Core responsibilities:

  • - Generate, review and authorize Quality related documents
  • - Lead and/or participate in (quality improvement) projects
  • - Maintain the CAPA (corrective and preventive actions) system
  • - Develop and conduct Quality and Quality improvement trainings for NL employees
  • - Execute and follow up internal and external audits
  • - Release products, processes and equipment

Typically this person will be degree qualified to Bachelor level with solid experience in QA within the Medical Devices sector or similar over a number of years including maintaining and improving Quality management systems to ISO 13485. FDA 21CFR820, MDD 93/42EEC or similar. QA experience should be within production level and preferably include EO sterilization, and also Cleanrooms and microbiology exposure. Participation or leading of Audits to ISO 13485 is essential, as are both English and Dutch language skills.

For more information on this exciting opportunity, or any other medical device opportunities, please contact the Senior Consultant Andrew Boroky on 0044 (0) 207 940 2116, or email him at

Posted: 11/08/2012 | NPJ Ref: 84896
line graphic

Compatible with:

JobMate   Broadbean

Site optimised for Internet Explorer 8+ / Firefox 3+
View a complete Jobs Listing

Credit cards image