22.09.24 | 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 | 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 ansehen16.09.24 | Vollzeit | Couvet | JobLeads GmbH | CHF 80’000 - CHF 100’000 Of experience in Quality Assurance, Quality Control, and/or Regulatory Affair 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
Später ansehen11.09.24 | Vollzeit | Neuchâtel | Randstad Schweiz AGThe application of industry specific compliance standards/regulations to - assays life cycle management activities - Participate to daily activities upon request (provide technical and statistical support) Your profile - University or engineering degree in analytical chemistry, biotechnology, biochemistry - 1
Später ansehen06.08.24 | Vollzeit | Le Locle | Randstad Schweiz AGEnsure that all projects are in compliance with cGMP, cGLP, QSR (including Design Controls), ISO or other applicable requirements. - Support and address comments and suggestions associated with validation and engineering documentation. - Protocol, Deviation, and summary report generation and approval
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