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- ...Laboratory Technician Quality Control 80-100% Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist. Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen...QualitätSelbständige Tätigkeit
- ...support our clients in developing differentiated stable usable and safe injectable treatments for patients. Your mission Join our Quality Leadership Team in Visp Switzerland! We are looking for two QA Product Quality Stewards to drive excellence across our project...QualitätVollzeit
- ...Laboratory Data Review Specialist Quality Control, parttime 40% Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist. Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir...QualitätTeilzeitarbeitSelbständige Tätigkeit
- ...programs aligned with cGMP/Annex 15 and internal SOPs. Support Quality Systems activities: Document Management, Change Control,... ...Collaborate cross-functionally (Engineering, Production, QA, EHS) and help shape requalification and preventive maintenance plans...Qualität
- ...operating instructions / work instructions / SOP) Safe and accurate execution of work in compliance with safety regulations and cGMP quality requirements Responsibility for cleanliness and order in the workplace as well as the assigned rooms and warehouses Every...QualitätSchichtarbeit
- ...facilities in Visp. You will play a crucial role in the network between the different departments such as development, manufacturing, quality assurance and quality control. Become part of this exciting opportunity and apply now! What you will get: An agile career and...Qualität
- ...Assignment in various functions within the production facilities in compliance with safety regulations and consideration of cGMP quality requirements. Recognition, interpretation and elimination of deviations Execution of production steps incl. recording and calculations...Qualität
- ...Compliance Expert to join their team in Visp. We need someone who treats Auditing as an art form, Compliance as a religion, and the Quality Management System (QMS) as their personal masterpiece. If you can stare down a regulatory inspector with a calm smile and a...Qualität
- ...greenfield manufacturing site. This is a rare opportunity to shape a facility from the ground up ensuring it meets the highest standards of quality and patient safety. Your responsibilities will include As a Qualification Engineer you are responsible for defining CQV...QualitätVollzeit
- ...usable and safe injectable treatments for patients. Your mission We are looking for a Senior QMS & Compliance Expert to join our Quality Assurance team in Visp. You will play a key role in driving inspection readiness and management robust Quality Risk Management (QRM...QualitätVollzeit
- ...GMP standards and ensuring a smooth production flow this role offers you the chance to be a crucial link in the success of our high-quality pharmaceutical production. As a Shift Coordinator you are a crucial pillar in our production process. Your area of...QualitätVollzeitSchichtarbeitTagschicht
- ...changeovers of the filling plant. Ensuring complete precise documentation of all manufacturing steps and adherence to the strictest quality standards through product controls using laboratory equipment. Joint responsibility for the strict adherence to all regulatory...QualitätVollzeitSchichtarbeit
- ...stable usable and safe injectable treatments for patients. Your mission We are seeking a dynamic and highly experienced Head of Quality & GMP Operations to lead and evolve our Quality Management Systems (QMS) and ensure unwavering compliance within our manufacturing...QualitätVollzeit
- ...and safe injectable treatments for patients. Your mission We are looking for a dedicated QA Manufacturing Specialist to be our quality champion on the manufacturing shop this role you will play a critical part in maintaining Good Manufacturing Practices (GMPs)...QualitätVollzeitSoforteinstellung
- ...observer; youll be embedded with Subject Matter Experts (SMEs) tackling critical projects from day one to ensure the highest standards of quality for innovative life-changing biopharmaceuticals. **Please note that we are unable to provide visa sponsorship for this position....QualitätVollzeitSoforteinstellung
- ...gap analyses and continuous improvement across the validation lifecycle; apply lessons learned and regulatory updates. Perform Quality Systems activities: Document Management, Change Control, Non-conformities/Deviations, CAPA; write/revise procedures (SOPs/WIs)....QualitätVollzeit