22.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 CSV Expert with experience in QC Analytical Instrument and Lab. Computerized System Validation. Start Date ASAP/October 14th 2024 Contract Duration 12 months (extension is possible) Location Neuchatel Duties - The job holder is accountable for life cycle management activities of systems used
Später ansehen17.09.24 | Vollzeit | Boudry | JobLeads GmbH | CHF 80’000 - CHF 100’000 Manager Site Project Management Apply at locations Boudry - CH Time type Full time Posted on Posted 30+ Days Ago Job requisition ID R1584270 Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb
Später ansehen15.09.24 | Vollzeit | St-Sulpice (NE) | JobLeads GmbH | CHF 125’000 - CHF 150’000 And clinical studies. - provide leadership for Design Controls compliance and maintenance of Design History Files. - Contribute to and establish product development policies such as the Quality Management System and ensure adherence to it during the design and development processes. - Identify and manage
Später ansehen18.09.24 | Vollzeit | Neuchâtel | Randstad Schweiz AGIs accountable for life cycle management activities of systems used in the QC Laboratories. - Analytical Instrument Qualification - Computerized System Validation In addition, the job holder also supports the Data Integrity deployment. - Validation and Qualification Activities - Author specification documents
Später ansehen11.09.24 | Vollzeit | Neuchâtel | Randstad Schweiz AGFor our client, an international company in Neuchâtel, we are looking for a QC Associate Scientist. - Start dateASAP - Contract for 6 months via Randstad - Extension possible - Workplace Neuchâtel - Workload 100% Responsibilities The job holder is accountable for life cycle management
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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