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- Lonza Visp, Switzerland What you will do: Lead and deliver customer programs across their full lifecycle - from technology transfer to GMP manufacturing and project closure - ensuring quality, timelines, and cost-effectiveness. Act as a trusted partner...Suggéré
- 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...SuggéréTemps plein
- About the role We’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical... ...(e.g., Veeva, TrackWise, MasterControl). Exposure to data integrity principles (ALCOA+), Annex 11/Part 11, and CSV/CSA approaches....Suggéré
- 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...SuggéréRemote 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...SuggéréTemps pleinRecrutement immédiat
- ...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...Suggéré
- ...Manpower CAPEX Project Buyer (a) ? Pharma / Engineering ? 80-100% ? Visp For our client, an international pharmaceutical/biotech company based in Visp, we are currently looking for a motivated and detail-oriented: CAPEX Project Buyer (a) In this exciting...Suggéré
- ...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...SuggéréRecrutement immédiat
- ...data packages and sustainable control strategies. What we are looking for: University degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences or a comparable discipline; Solid experience in a GMP‑regulated environment, ideally within Small Molecule...Suggéré
- ...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,...Suggéré
- ...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...SuggéréTemps plein
- ...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...Suggéré
- ...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...SuggéréTravail à domicile
- ...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...Suggéré
- ...oversee complex analytical projects, drive method development and validation activities, and ensure the highest standards of data integrity and regulatory compliance. You will collaborate closely with cross-functional partners - including Manufacturing, Quality Assurance...Suggéré
- ...an. Zudem besteht die Möglichkeit, in einer touristischen Berggemeinde saisonale Praxiseinsätze zu leisten. Sie wünschen sich eine integre Persönlichkeit mit hoher Sozialkompetenz, allenfalls auch ein Familienmensch oder ein Mensch mit Familie. Es erwartet Sie ein...Temps pleinTemps partielAutomne
CHF 80000 - CHF 100000 par année
...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...Temps pleinFreelanceTravail posté- ...management team to ensure transparency and accountability in operations. Implement and maintain security protocols to protect the integrity of the data center infrastructure, ensuring compliance with industry standards and best practices for data security....Temps pleinFreelanceRemote jobHoraire flexible