QA Manager
Gent, Belgium
2 dagen geleden

SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation.

We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies.

By using highly advanced algorithms, we enable our team of Resource & Data Strategists to maintain the most advanced, detailed and complete Life Sciences network in Europe.

This big data enables us to work Reverse Recruitment : we first analyze the market in-depth before we go out to the market.

Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment , making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical and Medical Devices organisation, based in West-Vlaanderen Belgium.

The Company

For a very interesting pharmaceutical company I am looking for a qualified QA Manager.

Role Description

As a QA Manager and Responsible Person you are responsible for GDP (Good Distribution Practices) requirements for the different countries in which the company carries out distribution activities for medicines.


  • You are responsible for the follow-up and implementation of new legislation and quality standards.
  • You optimize the quality management system, processes and procedures with the objective of optimizing the functioning of all quality processes.
  • You support both internal and external quality audits and you implement the necessary actions resulting from these audits.
  • You coordinate and investigate quality issues such as non-conformities, complaints about product quality, etc. You prepare action plans and adjust where necessary.
  • Requirements

  • Masters in Pharmaceutical Sciences, Medicine, Chemistry or similar.
  • You have a thorough knowledge of QA systems and GxP requirements, including regulations and standards that affect medical devices, nutritional supplements and other pharmaceutical products.
  • You are analytical and think problem solving with a focus on continuous improvement.
  • You have strong communication skills in Dutch / English and preferably French
  • Other information

    Are you interested or do you want to know more about this position? Do not hesitate to call me, reply to this message or send an e-

    mail to j.zanting !

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

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