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Quality Engineer Temp (6-12 months)

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The company

Our client is a professional organisation, based in Oost-Vlaanderen Belgium. The company has over 50 years of experience in developing and manufacturing pharmaceutical products world wide.

Role description

In this temporary you will be working within the quality team.


You review and approve technical documentation generated during the development process & improvement projects
You participate to design review meetings & act as quality expert
You write and/or approve changes & CAPA’s.
You own and maintain the product risk management file
You handle and follow-up product complaints from end users, affiliates, distributors and partners
You optimize, validate and implement QC methods and procedures
You discuss complaints which could have consequences on public health and liaise with the Risk Assessment Committee
You provide support to the QC department


Master degree in bio-environment
Project management experience
3 years quality experience in pharmaceutical or diagnostic environment
Insight in customer & market requirements
Fluent in both English and Dutch
Good written and oral communication skills
Positive, pro-active and flexible attitude
Team player: open minded, cooperative, takes initiative
Good problem solving - problem analysis

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 Greg Silberstein

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SIRE Life Sciences®

Ref. nummer: 47923
Geplaatst door: SIRE Life Sciences®
Geplaatst op: 12-06-2019
Land: Belgium
Regio: Oost-Vlaanderen
Dienstverband: Permanent
Expertise: 3 - 5 jaar
Locatie Type: Op locatie
Opleiding: Master
Taal: Nederlands
Sector: Pharmaceutical
Specialisatie: Quality

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