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- ...Title: Quality Specialist Location: Visp, Valais, Switzerland (On-site) We are looking for a Quality Specialist with experience... ...Completed university degree in Pharmacy, Biotechnology, Chemistry, Engineering, or a related field. At least 5 years of experience in a...Empfohlen
- ...an experienced Commissioning, Qualification & Validation (CQV) Engineer to support validation activities within a highly regulated pharmaceutical... ...regulations. You will collaborate closely with engineering, quality, and operations teams to ensure that equipment and...EmpfohlenVollzeit
- About the role We’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical... ...aligned with cGMP/Annex 15 and internal SOPs. Support Quality Systems activities: Document Management, Change Control, Deviations...Empfohlen
- 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
- 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
- ...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
- ...Manpower CAPEX Project Buyer (a) ? Pharma / Engineering ? 80-100% ? Visp For our client, an international pharmaceutical/biotech... ...activities and work closely with Engineering, Project Management, Quality, and Finance teams. Your Responsibilities Support...Empfohlen
- ...Switzerland, you will play a key part in safeguarding product quality and patient safety by driving risk‑based impurity compliance for... ...looking for: University degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences or a comparable discipline; Solid...Empfohlen
- ...Act as a key interface between Production, QA, Monitoring, Engineering and EHS in the field of contamination control Plan, lead and... ...requests (CRs) Ensure timely closure of deviations in line with quality system requirements Identify and implement improvement...Empfohlen
- ...plus The role Join a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities... ...; apply lessons learned and regulatory updates. Perform Quality Systems activities: Document Management, Change Control, Non-conformities...EmpfohlenVollzeit
- ...key accounts, and evaluate new suppliers to ensure capacity and quality. Project Management: Act as a core member of the Global... ...ancillary costs. Qualifications Education: Preferably an Engineering degree by training. An advanced degree in Supply Chain,...EmpfohlenHomeoffice
- ...treats Auditing as an art form, Compliance as a religion, and the Quality Management System (QMS) as their personal masterpiece. If... ...it’s not just a collection of binders, but a living, breathing engine of excellence. System Ownership: Take the wheel on Deviations...Empfohlen
- ...responsible for the cleaning validation related activities in our biopharmaceutical plant and help ensure the highest standards of quality and compliance. Key responsibilities: Develop and coordinate equipment cleaning validation strategy and activities for...Empfohlen
- ...Lonza Visp, Switzerland The Senior Scientist in Quality Control serves as a scientific and strategic leader within the QC organization. In this role, you will oversee complex analytical projects, drive method development and validation activities, and ensure...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
- ...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 and main point of contact for customers, fostering transparent...
- ...laboratory work, driving upstream development activities and collaborating with cross-functional teams and customers to deliver high-quality bioprocessing solutions. Key responsibilities: Lead, design, and execute complex upstream process development...
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...VollzeitFreelanceSchichtarbeit