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QMS Specialist - Antwerp - 6 Month Contract
Eingestellt von Optimus Search
Gesuchte Skills: Design
Projektbeschreibung
QUALITY MANAGEMENT SYSTEM SPECIALIST - ANTWERP - 6 MONTH CONTRACT
A leader in the medical device industry, located in Antwerp, is in need of a Senior Quality Systems Specialist to integrate a Quality Management System. This will be an initial 6 month contract, but extension is highly likely.
THE SENIOR QUALITY SYSTEMS SPECIALIST WILL HAVE THE FOLLOWING RESPONSIBILITIES:
- Perform compliance reviews to Quality Management System requirements on new or updated documents
- Act as a liaison between corporate and the business units
- Design, prepare and distribute reports related to QMS processes and projects
- Work with local and remote teams to ensure QMS compliance
- Provide training on QMS to ensure understanding of the QMS
THE SENIOR QUALITY SYSTEM SPECIALIST MUST MEET THE FOLLOWING REQUIREMENTS:
- Bachelor's degree
- Strong experience with ISO13485
- Experience managing and working with a Quality Management System (QMS) within a regulated industry (medical device preferred but also open to pharmaceutical, biologics and aerospace)
- Excellent communicator
- Able to coach and train individuals
If interested please respond with an updated C.V.
A leader in the medical device industry, located in Antwerp, is in need of a Senior Quality Systems Specialist to integrate a Quality Management System. This will be an initial 6 month contract, but extension is highly likely.
THE SENIOR QUALITY SYSTEMS SPECIALIST WILL HAVE THE FOLLOWING RESPONSIBILITIES:
- Perform compliance reviews to Quality Management System requirements on new or updated documents
- Act as a liaison between corporate and the business units
- Design, prepare and distribute reports related to QMS processes and projects
- Work with local and remote teams to ensure QMS compliance
- Provide training on QMS to ensure understanding of the QMS
THE SENIOR QUALITY SYSTEM SPECIALIST MUST MEET THE FOLLOWING REQUIREMENTS:
- Bachelor's degree
- Strong experience with ISO13485
- Experience managing and working with a Quality Management System (QMS) within a regulated industry (medical device preferred but also open to pharmaceutical, biologics and aerospace)
- Excellent communicator
- Able to coach and train individuals
If interested please respond with an updated C.V.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design