23.09.24 | Vollzeit | Boudry | JobLeads GmbH | CHF 100’000 - CHF 125’000 At work and in their personal lives. At Bristol Myers Squibb, we are inspired by a single vision - transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate
Später ansehen23.09.24 | Vollzeit | Couvet | JobLeads GmbH | CHF 80’000 - CHF 100’000 And/or Regulatory Affairs in a pharmaceutical company or other related industry. - Bachelor's degree in Pharmacy, Chemistry, Microbiology or related science. Knowledge - Skills - Abilities - Thorough understanding of cGMPs and Swiss, EU, and FDA regulatory requirements. - Demonstrated experience in Regulatory
Später ansehen22.09.24 | Vollzeit | Neuchâtel | Hays AGWith over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated
Später ansehen22.09.24 | Vollzeit | Couvet | JobLeads GmbH | CHF 80’000 - CHF 100’000 And/or Regulatory Affairs in a pharmaceutical company or related industry. - Bachelor's degree in Pharmacy, Chemistry, Microbiology, or related science. Knowledge - Skills - Abilities - Thorough understanding of cGMPs and Swiss, EU, and FDA regulatory requirements. - Demonstrated experience in Regulatory
Später ansehen22.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Validation experience in the biotechnology or pharmaceutical industry. - Extensive experience with validation life cycle requirements for cGMPs laboratory systems. - Experience with project management and/or leadership enabling cross-functional engagement to deliver project goals and timelines. - A thorough
Später ansehen22.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Deviations and investigations - Serve as SME for internal technical group discussions Minimum Requirements - Master’s in engineering, Computer Science, or related technical field - Solid validation experience in the pharmaceutical industry - Experience with validation life cycle requirements for cGMPs
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