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Job Description SummaryWork in the Sterile Area for aseptic manufacturing in accordance with the GMP requirements, Novartis SOPs and production documentation. Job Description Key responsibilities: Responsible for the control of Raw Materials (MP) for the manufacturing of
Work in the Sterile Area for aseptic manufacturing in accordance with the GMP requirements, Novartis SOPs and production documentation. About The Role Key responsibilities include: Control of Raw Materials (MP) for the manufacturing of the sterile batch (e.g.
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