水平: Associate

工作类型: Full-time

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工作内容

Our customers are located in Puurs, Flanders.

As a quality control specialist, you are responsible for the proper execution of the missions for which you are responsible.

In your daily work:

  • You actively contribute to the establishment and implementation of CAPAs related to laboratory compliance resulting from audit observations;
  • You manage QC testing to support commercial manufacturing;
  • You write and support SOPs related to test programs, laboratory operations and/or equipment operations;
  • You ensure that quality systems (deviation, OOS investigation, CAPA, documentation, training, change control, validation activities, maintenance and calibration activities) are in place and managed;
  • You communicate quality control information to all relevant organizational departments, external suppliers or subcontractors.

What we offer:

  • A permanent contract;
  • A very large portfolio of pharmaceutical, biotechnology, medical equipment, chemical and energy customers;
  • Projects going from short term (minimum 3 months) to long term (minimum 1 year);
  • A salary package over 13.92 months including a company car, insurance, representation expenses, etc. Remuneration is negotiable and varies according to level of experience and skills.

Description of the profile:

  • You hold a Master’s degree and have at least 3 years of professional experience in the pharmaceutical industry or biotechnologies or medical devices;
  • You know analytical techniques such as HPLC, PCR, GC;
  • You have an analytical mind and are able to translate complex processes into clear and compliant procedures;
  • You organize your work efficiently and know how to manage deadlines;
  • You have a good level of French and/or Dutch and a good knowledge of English.
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最后期限: 31-12-2025

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