17.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Product impact assessment in protocols/studies deviations related to product, - process/ equipment improvement projects including technology transfer, - small scale/scale down product validation activities, - writing of reports /review of documents and reports. - Manage documentation associated
Später ansehen17.09.24 | Vollzeit | Boudry | JobLeads GmbH | CHF 80’000 - CHF 100’000 Manager Site Project Management Apply at locations Boudry - CH Time type Full time Posted on Posted 30+ Days Ago Job requisition ID R1584270 Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb
Später ansehen16.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 In protocols/studies deviations related to product, - process/ equipment improvement projects including technology transfer, - small scale/scale down product validation activities, - writing of reports /review of documents and reports. - Manage documentation associated with laboratory activities. - Control
Später ansehen15.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Quality Systems Expert at our Neuchatel site, you will report to the Quality Systems Manager. Your responsibilities will include managing documentation and quality systems integration to align with Takeda's policies and global cGMP requirements. Our mission is Management of Quality Systems You
Später ansehen15.09.24 | Vollzeit | Le Locle | JobLeads GmbH | CHF 80’000 - CHF 100’000 Including cleaning, to ensure their effectiveness in producing clean and safe products - Supporting the validation of treated water, controlled environment, and finishing/cleaning processes - Guiding plant personnel as needed to ensure good manufacturing and documentation practices - Assisting
Später ansehen15.09.24 | Vollzeit | St-Sulpice (NE) | JobLeads GmbH | CHF 125’000 - CHF 150’000 And clinical studies. - provide leadership for Design Controls compliance and maintenance of Design History Files. - Contribute to and establish product development policies such as the Quality Management System and ensure adherence to it during the design and development processes. - Identify and manage
Später ansehen18.09.24 | Vollzeit | Neuchâtel | Randstad Schweiz AGIs accountable for life cycle management activities of systems used in the QC Laboratories. - Analytical Instrument Qualification - Computerized System Validation In addition, the job holder also supports the Data Integrity deployment. - Validation and Qualification Activities - Author specification documents
Später ansehen06.08.24 | Vollzeit | Le Locle | Randstad Schweiz AGCompetent in tracking and updating schedules to provide upper management visibility of milestones and achievements. - Use of Microsoft office tools - Knowledges of
Später ansehen22.02.24 | Teilzeit, Vollzeit | Schaffhausen | Michael Page InternationalAre seeking a Process Safety Specialist to lead the process safety management system and provide technical support to production and R&D teams. The ideal candidate will have a background in Chemical Engineering, 5 years of experience in chemical process safety, and fluency in French and English
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