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Quality Officer/ Responsible Person

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The company

Our client is a professional Pharmaceutical and Biotechnology organisation, based in Noord-Brabant Netherlands. A international pharmaceutical client who is driving by the commitment to patients. The client brings innovative products, services and solutions throughout people around the world.

Role description

The Pharmaceutical Quality Officer is part of the Business Quality Department Benelux. He/she plays an important role in the implementation and maintenance of Quality Systems. He/she holds ownership of those systems and contributes to the continuous improvement of the Pharmaceutical Quality aspects of our business.
As a registered Responsible Person (RP) the Pharmaceutical Quality Officer Benelux

Responsibilities

- Act as local process owner for event and deviation management, CAPA management and change management systems
- Act as back-up for the Head of Quality, focussing on product quality complaint handling and product issue handling, recalls and field actions
- Assist in GxP inspections and audit preparation and provide support during actual inspection /audit execution
- Ensuring that new / revised quality management systems are implemented and maintained
- Guide the local Product Quality Review process, assuring compliance with the EU GMP guidelines and J&J Business Quality requirements
- Together with QA associate QMS, take leadership in document management processes.
- Act as primary contact for the European Distribution Center regarding batch version and batch status management
- Coordinating and performing promptly any recall operations
- Ensuring that relevant customer complaints are dealt with effectively
- Authorizing the return to saleable stock of any returned medicines

Requirements

- Preferably 2 years of experience in pharmaceutical or related industry, ideally with a mix of manufacturing / Distribution / QA operations experience.
- Understanding of pharmaceutical product development, qualification, manufacturing, packaging, validation, testing, release and distribution processes and their relation to the marketing authorization process.
- Up-to-date knowledge of relevant pharmaceutical legislation, directives and guidelines, GMP/GDP and SOP’s.
- Ability to work independently, systematically and orderly with great accurateness.
- Strong analytical, communication and decision-making skills.
- Creative and pro-active team player.
- Thorough command of the Dutch, English and preferably French language.

Other information

Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Seppe Verhoeven


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SIRE Life Sciences®

Ref. number: 5726
Listed by: SIRE Life Sciences®
Listed on: 13-06-2019
Country: The Netherlands
Region: Noord-Brabant
Employment: Freelance
Expertise: 3 - 5 years
Location Type: On location
Education: Bachelor
Language: Dutch
Sector: Pharmaceutical
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 Belgium BVBA

Science 14 Atrium
14b, Rue de la Science
1040 Bruxelles
+32 (0) 2 588 1277

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80333 München
+49 (0) 89 3803 8966

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+44 7307 179882

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