21.05.24 | Vollzeit | Zürich | BakerHicksBiotech, OSD, Secondary Manufacturing, Cell & Gene Facilities), from concept development to commissioning of the qualified plant Project assignments as process lead in the above-mentioned areas, managing and coordinating process engineering teams Development of the essential process-technical basics
Später ansehen21.05.24 | Vollzeit | Bern | CSL BehringWith GxP requirements Support the validation and lifecycle management of laboratory automation systems and software applications Maintain working knowledge of regulations and guidelines as related to laboratory instrumentation and computerized systems (i.e. USP, 21CFR Part 11, Annex 11 regulations
Später ansehen21.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalFor products manufactured at Neuchâtel facility. Participate in GMP (Good Manufacturing Practice) tours of facility to ensure inspection ready status. Interaction with authorities Act as a “Subject Matter Expert” (SME) in the creation and modification of regulatory license sections for products manufactured
Später ansehen21.05.24 | Vollzeit | Zürich | Takeda PharmaceuticalRegulations, such as Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Clinical Practice (GCP). How you will contribute Partner across departments and international manufacturing sites to deliver on time and within budget. D evelop, track and measure key performance indicators mid
Später ansehen21.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalOf activities all along the manufacturing and release process. How you will contribute QA Expert Act as QA(Quality Assurance) representative for both routine GMP (Good Manufacturing Practice) activities and Takeda projects. Act as the Quality partner within Production Unit Team and the Quality Control
Später ansehen21.05.24 | Vollzeit | Luzern | Sazerac SwitzerlandComply with audit response requirements. · Conduct quality management system audits at internal plants, suppliers, co-manufacturers and co-packers to identify gaps in the systems and opportunities to improve quality and food safety. Qualifications Bachelor's or Master’s Degree in Engineering, Food
Später ansehen21.05.24 | Vollzeit | St. Gallen | CSL ViforHealthcare, aiming to help patients around the world lead better, healthier lives. We are currently looking for a QA Manufacturing Science Manager for our Parenteral Products to join our team in St. Gallen. In this exciting position, you will be in charge of the Quality oversight of GMP data trending
Später ansehen21.05.24 | Vollzeit | Bern | CSL BehringWith GxP requirements Support the validation and lifecycle management of laboratory automation systems and software applications Maintain working knowledge of regulations and guidelines as related to laboratory instrumentation and computerized systems (i.E. USP, 21CFR Part 11, Annex 11 regulations
Später ansehen16.05.24 | Vollzeit | Monthey | RM Group AGLaboratory research activities, recording observations and measurements, and reporting results - Maintaining cleanliness and operational efficiency of cleanrooms and equipment, including coordination with third-party cleaning vendors - Managing receipt, inspection, and stocking of raw materials
Später ansehen20.05.24 | Vollzeit | Baar | Glencore International AGAs a Personal Assistant, you will be a permanent employee of our Finance Team. In this position, you will be in charge of various administrative tasks as described roleCalendar management, scheduling meetings and conference calls incl. virtual data room preparationCarrying out travel
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