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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.
- 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).
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