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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
- ...Für die Lonza AG in Visp suchen wir ab sofort eine/n Bioprocess Engineer 100% (w/m/d) Deine Kernaufgaben Kampagnenleitung: Du verantwortest die Herstellung von Biokonjugaten unter cGMP-Richtlinien Prozess-Support: Du sicherst die Chargenausführung, löst technische...EmpfohlenSoforteinstellung
- ...Ihre Aufgaben Planung und Durchführung von technischen Teilprojekten im Anlagenumfeld, inkl. Prozessoptimierung und Engineering-Berechnungen Erstellung von Machbarkeitsanalysen und Konzeptstudien für Neu- und Umbauten, inkl. Budget- und Zeitplanung Durchführung...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
- 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
- ...Material & Chemical Management: Complete material checklists to ensure availability of required consumables Notify Bioprocess Engineers of missing chemicals or discrepancies Conduct ethanol aliquotation in compliance with GMP and safety requirements Support...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
- ...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
- ...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
- ...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
- ...IAM Reduce operational risk by eliminating legacy and end-of-life system dependencies Coordinate stakeholders across IT, OT, Engineering, QC, Logistics, and Security Manage project scope, timeline, budget, risks, and reporting Ensure delivery aligns with IT...Empfohlen
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