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Manufacturing Supervisor

  1. North
  1. Contract
AB 23044
  1. Life Sciences
Date Posted14 Aug 2019
Manufacturing Supervisor – The Netherlands – Global Pharmaceutical Manufacturer

I am currently working with a Global CDMO within the Pharmaceutical Industry who have a requirement for a Manufacturing/Production Supervisor.

The client is looking for someone with 3+ years’ experience working within a GMP manufacturing organisation and specific knowledge of upstream manufacturing.

The Supervisor will be responsible for the following:
  • Responsible for timely and within budget execution of production activities according to cGMP requirements, and contribute to the overall departmental objectives.
  • Hand over each shift effectively, ensuring that all relevant production issues have been brought to the attention of successor.
  • Responsible for proper administration within team.
  • Participate in daily production meetings and align the way of working within the team and with colleagues; propose changes in SOP / production schedule when more efficiency can be achieved and review production documentation.
  • Participate in daily production meetings and align the way of working within the team and with colleagues.
 Required Level of Experiences
  • At least 3 years of operational experience in a (bio)pharmaceutical company.
  • Knowledge of pharmaceutical cGMP systems.
  • Relevant knowledge of process unit operations (e.g. cell culture, chromatography, filtration).
If this role is something you would like to learn more about please submit your CV and I will be in touch at my earliest convienience.

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