25.04.24 | Vollzeit | Bern | Randstad Schweiz AGAnd procedures are managed effectively. Requirements - Bachelor's or master's degree in technical or natural sciences. - Minimum 3 years of working experience within pharma or biotech. - Minimum 4 years of working experience with CSV. - Knowledge of FDA 21CFR part 11/EUGMP Annex 11 regulations and ISPE GAMP 5
Später ansehen22.04.24 | Vollzeit | Bern | Randstad Schweiz AGBased viral- and bacterial vaccines and bacterial based therapeutic products. Main Responsibilities - Manage projects and activities related to materials compliance (Material assessment for new product introduction) - Serve as liaison between Suppliers, Material science and Supplier Quality
Später ansehen10.04.24 | Vollzeit | Bern | Randstad Schweiz AGDocuments like MBR, Work Instructions, Equipment manuals and Process Risk assessments - Writing of electronical Batch Records will be one of the main tasks at the beginning - Train Operators on written process documents - Support PPQ (Process Performance Qualification) - Managing of Quality Issues, Root
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