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- ...knowledge of working with Emerson DeltaV, Manufacturing Execution Systems (MES), and within a GMP-regulated environment in the pharmaceutical or biopharmaceutical industry. Strong team orientation Structured and proactive working attitude Open-minded for new ideas...Empfohlen
- ...or equivalent experience, or vocational education (EFZ, FH, HF, BSc.) Proven experience in the operation and maintenance of pharmaceutical plants or the biotech industry Proficiency in SAP, COMOS (Plant Engineering Software), DeltaV (Process Control System), and...Empfohlen
- ...monitoring systems Develop, create and implement EHS process safety standards for Visp Key requirements: Master’s Degree in Pharmaceutical Technology, Chemistry, Process Engineering, Biotechnology, or equivalent Safety Engineer (Sicherheitsingenieur) EKAS / SUVA...Empfohlen
- 0 Teilen For an international pharmaceutical company located in VISP we are looking for a CQV Lead: JOB DESCRIPTION Provide leadership of CQV activities in assigned Projects together with PM, Process Engineers and QA Act as subject matter expert (SME) on CQV standards...EmpfohlenSoforteinstellung
- ...Track and control QC project costs Competences ~ Master's or PhD in biology, biochemistry, pharmaceuticals, or a related natural science ~3-5 years of experience, ideally in a GMP environment and Quality Control ~ Strong communication...EmpfohlenVollzeitHomeoffice