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For our client Merck based in Aubonne, we are looking for a QA Engineering Expert for a duration of 9 months (until 31.12.2024).Your role:Ensure that equipment & automated systems implemented are in accordance with internal procedures and current guidelines/regulations (including procedures related to change, risk and deviation management)Support Equipment and Automated Systems deviation management.Support, review and approve change control proposal (CCP)

Pour notre client spécialisé dans les technologies médicales, englobant divers secteurs chirurgicaux tels que l'orthopédie, la neurochirurgie, la chirurgie générale et reconstructive, nous recherchons un(e) :Ingénieur/technicien en Lean Manufacturing (contrat temporaire indéterminé)  Au sein du département d'amélioration continue vous intervenez en tant que professionnel en Lean manufacturing.Vous possédez une expertise dans la gestion des fournisseurs car

Are you ready to dive into the world of Regulatory Affairs and Quality Assurance ? We're on the lookout for a RA & QA Compliance Specialist to join a dynamic team and medical device company ! We are seeking a qualified candidate for the role of Regulatory Affairs and Quality Assurance Specialist. This position is integral to ensuring compliance with the EU Medical Device Regulation (EU MDR), Swiss Medical Devices Ordinance (Swiss MedDO), and relevant regul

For our client, an international company in Solothurn, we are looking for a Senior QA Release LeadStart date: 01.05.2024End: 31.12.2024Extension: must be discussedWorkplace: BaarWorkload: 100%Job SummaryAct as Responsible Person (RP) delegate for Commercial Biologics Drug Substances (DS), Parenteral Drug Products (DP), Parenteral Finished Goods (FG) technical release or Active Pharmaceutical Ingredients (API), Pharmaceutical Drug Products, Pharmaceuticals

Für die Welt sorgen … beim Einzelnen beginnen. Dieser Leitsatz inspiriert und eint die Menschen bei Johnson & Johnson. Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.Die Cilag AG ist ein internationales Entwicklungs- und Produktionsunternehmen der Pharmasparte von Johnson & Johnson und stellt an ihrem Produktionsstandort in Schaffhausen, Schweiz pharmazeutische, medizinische und chemische Produkt

We believe in science and technology as a force for good Science is at the heart of everything we do. It drives the discoveries we make and the technologies we create ? and it forms the basis of our future growth. Our ambition is supported by the launch of our new facility.Joining our Manufacturing Department, you will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced

For our client, an international company based in Bern, we are looking for a motivated CSV Engineer.  General Information: Start date: ASAPEnd date: 31.12.2024Extension: possible, to be discussedWorkplace: BernWorkload: 100%Home office: 3 days on-site presence is required; on demand it may increase  Key Responsibilities: In charge of Computer System Validation (CSV) activities for Technical Services department in order to ensure that:Validation phases are