25.04.24 | Vollzeit | Bern | RandstadAnd 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 ansehen29.04.24 | Vollzeit | Bern | Speedgoat GmbHToolsIndependent and professional collaboration with internal and external development teams and partner companiesTechnical support of production and product management in case of hardware obsolescence or component updatesPrepare and maintain detailed documentation of software architectures and interfaces
Später ansehen26.04.24 | Vollzeit | Bern | Speedgoat GmbHThe entire product development process, from requirements specification to production and sales start, while ensuring project a Project Manager R& D, you closely collaborate with Technologies development and product management teams, Production, Markets and Sales, but also with all other
Später ansehen22.04.24 | Vollzeit | Bern | Comet AGAnd deliver multiple IT Projects on time in a broad range of business problems and their various system solutionsStrong critical thinking and managerial skills, including management of remote staffBreak new ground with usWork on innovative solutions for global technical challengesBenefit from a modern
Später ansehen10.04.24 | Vollzeit | Bern | JobLeads GmbH | CHF 150’000 - CHF 200’000 Konstruktionszeichnungen zu lesen Passion für Suche nach Optimierungsmöglichkeiten sowie Spass am Erarbeiten von Hilfsmitteln Sehr gute Deutschkenntnisse und Kenntnisse in Englisch Techniker/Ingenieur mit technischer Grundausbildung und Weiterbildung Richtung Lean Manager, Lean Green Belt, Lean Black Belt, Value Stream
Später ansehen25.04.24 | 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 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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