QA supervisor

For one of your clients, located in the region of Antwerp, we are looking for an enthusiastic colleague to develop a career in the Quality Department.

  • Are you an Industrial Pharmacist?
  • Do you speak fluently English and Dutch?
  • Do you have a first experience in the Life Sciences and/or Quality Assurance

Then this might be the ideal job for you!

Job Description 

As Quality Supervisor, you will be part of the QA team responsible for supporting the implementation of a general integrated quality management system (GMP/GDP/GCP/…) by improving the current processes and assuring the product quality compliance.

Responsibilities 
  • You support the coordination of the quality systems (batch review and releases,deviation reporting, complaint handling, change control)

  • You create the Product Quality Reviews (PQR) and are responsible for the follow-up of ongoing process validations

  • You track events and deviations of the Product Quality + CAPA follow-up

  • You review the quality processes (according to GMP/GDP/GCP and SOPS)

  • You are responsible for the quality review of the yearly product data and propose possible optimization opportunities.

  • You assure the implementation of the local requirements

  • You have a variety of contacts internal (logistics, production, line-managers of different departments, consumer services, RA, ...) and external (clients, suppliers,… )

Profile 
  • You have a Scientific Master degree (Industrial Pharmacist), QP is a plus.

  • You have a first experience in the Quality Assurance and/or the Life Sciences

  • You can work with Quality Systems

  • You possess strong communication skills and are not afraid to be assertive when necessary

  • You are conscientious and quality-oriented, with an analytical mindset

  • You possess a good knowledge of languages: fluent in English, Dutch (French is a plus)

Contact Information 

Hilde Wolput
+32 15 21 11 04
hilde.wolput@valesta.com

 

Application form : QA supervisor

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