C& Q Engineer (m/f)
M+W Group
10 dagen geleden

Duties & Responsibilities

Responsibility within our project teams for the preparation and execution of all project commissioning and qualification activities in a variety of industries (Pharmaceutical, Biotech and Food).

Assistance in the elaboration of the VMP, URS and protocols or risk assessments with senior staff members.

Executing independently and within a project team the qualification protocols (DQ, IQ, OQ, PQ), as per predetermined acceptance criteria.

Execution and documentation verification of vendor or contractor packages to achieve streamlined C&Q activities during project execution.

Coordination with all involved parties within the M+W team and the client (Validation, QA, QC, ).

Establishment, follow-up and closure of all deviations and punchlist items.


  • Bachelor s or master s degree in science or engineering related to Biotechnology, (Bio)Chemistry or similar.
  • 2-5 years of relevant work experience in a C&Q role in the Pharmaceutical or Biotechnological industry.
  • Knowledge of pharmaceutical or biotech production methods is considered an asset.
  • Knowledge of the latest developments in the C&Q field and relevant legislation and industry standards (cGMP) is highly appreciated.
  • You are committed, flexible, accurate, communicative, motivated and well-organized.
  • You like working in a team but you can also function in an independent and safe way, you will be able to solve technical issues.
  • The Offer

    We offer a very interesting job with exciting career opportunities within an international company in the high-tech environment.

    Working at M+W means you have personal responsibility, and the possibility to work with qualified, experienced and highly motivated colleagues in multinational teams.

    If you appreciate open communication, flat hierarchies, flexible working hours and an attractive salary, then you've come to the right place!

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