22.09.24 | 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
Später ansehen21.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 And documenting Equipment and Software validation - Conducting and participating in risk assessments, root cause analysis and investigations Your experience/knowledge - 5+ years of relevant validation experience in the biotechnology or pharmaceutical industry - Solid skills in Data Integrity requirements
Später ansehen21.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 And documenting Equipment and Software validation - Conducting and participating in risk assessments, root cause analysis and investigations Your experience/knowledge - 5+ years of relevant validation experience in the biotechnology or pharmaceutical industry - Solid skills in Data Integrity requirements
Später ansehen17.09.24 | Vollzeit | Boudry | JobLeads GmbH | CHF 80’000 - CHF 100’000 Organizational skills with the ability to multi-task - Education/Experience/Licenses/Certifications - 5+ years of project management experience in a manufacturing environment (pharmaceutical industry preferred) - Proven experience in successfully leading medium projects or programs - Project management
Später ansehen15.09.24 | Vollzeit | Boudry | JobLeads GmbH | CHF 80’000 - CHF 100’000 Begeistern - Gute Kenntnisse von Qualifikationsprozessen im Pharma, Medizinischen und Produktionsumfeld - Starke Dokumentations- und Kommunikationskompetenzen - Sprachen Deutsch und Englisch fließend (in Sprache und Schrift), Französisch von Vorteil - Internationale Ausrichtung und Bereitschaft
Später ansehen18.09.24 | Vollzeit | Neuchâtel | Randstad Schweiz AGIn the biotechnology or pharmaceutical industry - Fluent in French and English (C1 written and spoken) - 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
Später ansehen11.09.24 | Vollzeit | Neuchâtel | Randstad Schweiz AGOr 2 years of experience in GMP pharma business activities, preferably in the scope of recombinant therapeutic product in pharmaceutical environment - Experience in GMP Laboratory activities - Good knowledge of method transfer - Good knowledge of critical reagent qualification - Experience in problem
Später ansehen06.08.24 | Vollzeit | Le Locle | Randstad Schweiz AGChange control, non-conformance and CAPA support. Your profile - Bachelor's Degree in Engineering (Biomedical, mechanical, chemical, or electrical) or Science (Biology, Chemistry). - 2 to 5 years of experience in a Validation or Quality Assurance role for a medical device or pharmaceutical environment
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