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Snr Quality Associate Medical Devices

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The company

Our client is a professional Medical Devices organisation, based in Antwerpen Belgium. This organization is internationally represented. They are one of the market leaders for the development of self-care products. They offer an extensive product portfolio and rapidly are expanding.

Role description

You will become part of an informal and dynamic business setting in which quality is set at a high standard. You will receive various responsibilities that are directed to maintain and improve the Quality Management System. In addition, you are responsible for the ISO 13485 standards and required documentation. You will be the key person to contact whenever there are any issues or questions about the Quality system, ISO standards and required documentation. Furthermore, you will gain insights into improvements and developments for the QA department.

Responsibilities

On a daily basis you are involved with overviewing and maintenance of the Quality Management System. In addition, on a daily basis you are involved with:
• Offering support for the development of strategic plans and implementation tools for the improvement of the Quality Management System
• Gain insight into possible points of improvements for the QMS according to ISO 13485 standards
• Support and guidance during internal and external audits
• Providing advice and support to management in set up of QA/RA processes
• Collecting and creating reports of outcomes from audits especially for CAPA’s
• Management and control of QMS documentation and reviewing these documents
• You will be on track with the latest developments and changes of QA within the Medical Devices sector, involving regulations & legislation such as the MDR and FDA

Requirements

• Bachelor or Master preferably in Life Sciences
• Minimal 3 years of experience within the Medical devices industry
• Minimal 2 years of experience with QA
• Proven experience with the maintenance and improvement of QMS
• Excellent knowledge of American and European legislation and regulations, in particular the MDD and MDR
• Fluency in English
• Critical scope and excellent analytical skills
• Team player, yet individual operator

Other information

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ewout de Jong.


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SIRE Life Sciences®

Listed by: SIRE Life Sciences®
Listed on: 17-06-2019
Country: Belgium
Region: Antwerpen
Employment: Permanent
Expertise: 6 - 10 years
Location Type: On location
Education: Master
Language: English
Sector: Medical Devices
Specialisation: Quality

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Contact

SIRE Life Sciences B.V.

Mondriaan Tower
Amstelplein 52, 25th floor
1096 BC Amsterdam
+31 (0) 20 658 9800

SIRE Life Sciences Deutschland GmbH

Fünf Höfe
Theatinerstraße 11
80333 München
+49 (0) 89 3803 8966

SIRE Life Sciences UK

702 Howard House Dolphin Square
SW1V3PQ London
+44 7307 179882

SIRE Staffing Solutions B.V.

Keizersgracht 440A
1016 GD Amsterdam
+31 (0) 20 658 9804

SIRE Life Sciences Consultancy B.V.

Wetenschapsstraat 14B
1040 Bruxelles
+32 (0) 2 588 1277