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- Role Overview We are looking for an experienced Commissioning, Qualification & Validation (CQV) Engineer to support validation activities within a highly regulated pharmaceutical manufacturing environment. In this role, you will contribute to the commissioning, qualification...EmpfohlenVollzeit
- Senior SAP Basis Engineer (Remote) We are seeking an experienced and proactive Senior SAP Basis Engineer to join a global IT team supporting complex SAP landscapes. In this role, you will be responsible for the administration, optimization, and reliability of SAP systems...EmpfohlenRemote job
- Senior Bioprocess Engineer (Biologics) Location: Visp, Switzerland — 100% on-site Function: Operations / Manufacturing Science & Technology (MSAT) Type: Full-time, permanent (immediate start possible)The opportunity A fast-growing biologics site is expanding...EmpfohlenVollzeitSoforteinstellung
- ...a leading international company in the pharmaceutical industry, we are currently looking for a motivated and experienced Project Engineer . Your Responsibilities Technical Project Management (approx. 60%) Plan and execute small to mid-sized investment projects...Empfohlen
- About the role We’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP...Empfohlen
- ...improvement and standardization of cleaning validation practices Your Profile Degree in Life Sciences, Biotechnology, Chemical Engineering, or related field Proven experience in GMP cleaning validation within pharmaceutical or biopharmaceutical manufacturing...EmpfohlenSoforteinstellung
- ...and continuous improvement of hygiene standards at the Visp site Act as a key interface between Production, QA, Monitoring, Engineering and EHS in the field of contamination control Plan, lead and execute hygiene-related projects (material transfer, gowning, cleaning...Empfohlen
- ...improvement of the quality management system. Requirements: Completed university degree in Pharmacy, Biotechnology, Chemistry, Engineering, or a related field. At least 5 years of experience in a quality function within the pharmaceutical or biotechnology industry,...Empfohlen
- ...Contract type: Full-time Language: German (mandatory); English a strong plus The role Join a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ...EmpfohlenVollzeit
- ...You’ll be the proud owner of the Quality Management System, ensuring it’s not just a collection of binders, but a living, breathing engine of excellence. System Ownership: Take the wheel on Deviations, Change Control, Document Management, and Training. Risk...Empfohlen
- ...LCC) optimization and the reduction of material, transport, and ancillary costs. Qualifications Education: Preferably an Engineering degree by training. An advanced degree in Supply Chain, Business, or Economics is a plus. Industry Experience: At least 3 years...EmpfohlenHomeoffice
CHF 80000 - CHF 100000 pro Jahr
...security) Respond to incidents and perform troubleshooting Maintain accurate documentation and asset tracking Collaborate with engineering and operations teams Participate in capacity planning and upgrades ~3+ years data center operations experience ~ Expert...EmpfohlenVollzeitFreelanceSchichtarbeit