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Job Summary Responsible for leading and governing Phase In / Phase Out (PIPO) initiatives across the product lifecycle to ensure controlled product changes and PIPO transitions, from a Supply chain perspective with a strong focus on
Eine führende Personalvermittlungsfirma sucht eine Technische Sterilisationsassistenz (m/w/d) in Solothurn für einen temporären Einsatz. In dieser Rolle bist du dafür verantwortlich, Medizinprodukte hygienisch aufzubereiten und mit modernen Hightech-Geräten zu arbeiten. Teamfähigkeit, Flexibilität und gute Deutschkenntnisse sind
Flexsis sucht für Roche in Basel einen Validation Manager. Ihre Aufgaben umfassen die Erstellung von Qualifizierungsdokumenten und die Begleitung von Validierungsaktivitäten. Sie sollten über mindestens 5 Jahre Erfahrung in der pharmazeutischen Industrie und Kenntnisse in Sterilisationsvalidierung
We are looking for a Qualification & Cleaning/Sterilization Validation Subject Matter Expert (SME) to join our Technology Lifecycle Excellence (TLE) team. In this role, you will lead and supervise qualification and validation activities across the site, ensuring
EMS - Electro Medical Systems is seeking a Quality Engineer to ensure compliance in biocompatibility and sterilization of reusable medical devices. This role involves reviewing documentation, supporting product release activities, and collaborating with R&D and Regulatory Affairs.
Onboard Infection Prevention Control System Committee Operations • Responsible for professional and effective Cross-functional IPCS Committee operations, required meeting preparations, Minutes of the Meetings, reporting this duty directly to Captain onboard who is the Chair of
Advanced Sterilization Products is seeking a dedicated professional to lead Phase In / Phase Out (PIPO) initiatives to ensure controlled product changes from a supply chain perspective. Candidates should have a Bachelor’s degree and 5–7 years of
Overview Responsible for leading and governing Phase In / Phase Out (PIPO) initiatives across the product lifecycle to ensure controlled product changes and PIPO transitions, from a Supply chain perspective with a strong focus on supply
International pharma company 18 months contract with extensionoption About Our Client Our client is a well-established organization within the pharma industry, renowned for delivering innovative solutions and maintaining a strong commitment to quality and compliance. Operating
Founded in 1921 and headquartered in Mendrisio (Switzerland), Sinteticas mission is to continuously strive to improve therapies by enhancing its products formulations and usability for the benefit of clinicians and patients. We do so in close
MISSION As a Quality Engineer, you will report to the Quality Assurance Group Leader and act as an internal expert in biocompatibility, sterilization, and reprocessing of reusable medical devices. You will contribute to ensuring compliance with applicable
Projekt: Für unseren Kunden, ein grosses Pharmaunternehmen mit Sitz in Basel suchen wir einen Validation Manager / Ingenieur Reinigungs Hintergrund: Basel Drug Substance Manufacturing produziert in zwei Produktionsgebäuden in unterschiedlichen Massstäben biotechnologische „Large Molecule“ APIs (Active
Einleitung Du liebst komplexe Maschinen, saubere Prozesse und Verantwortung beim Kunden? Unser Auftraggeber ist ein führender Anbieter in der Blow-Fill-Seal (BFS) -Technologie für aseptische Abfüllung in der Pharma- und Kosmetikindustrie . In dieser Rolle übernimmst du
LHH is seeking a Qualification & Cleaning/Sterilization Validation Subject Matter Expert (SME) in Zug, Switzerland. This pivotal role involves leading qualification and validation activities, ensuring regulatory compliance, and representing the TLE team in cross-functional forums. The ideal