23.04.24 | Vollzeit | Visp | Randstad Schweiz AGExperience in document control for CAPEX projects within the pharmaceutical industry, with a strong understanding of GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and other relevant regulations. - Experiences with document control systems (Kneat or similar) - Excellent organizational
Später ansehen16.04.24 | Vollzeit | Zug | AdeccoAnd safety standards of pharmaceutical products in a highly regulated and rewarding environment. If you are passionate about precision, accuracy, and contributing to the advancement of healthcare, we invite you to explore this career opportunity with our client. Responsibilities - Conducting incoming goods
Später ansehen21.09.22 | Vollzeit | Zürich | Jobtic SATo develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory
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