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Our client is looking for a Quality Operations Technician to ensure products manufactured by external suppliers and contract manufacturers consistently meet quality, regulatory, and business requirements. The role combines operational quality oversight, supplier collaboration, batch release activities, and continuous improvement within a highly regulated medical technology environment.
The Senior Clinical Trial Assistant provides essential operational and administrative support across all phases of clinical studies. This role ensures high-quality documentation, compliance with regulatory standards, and smooth collaboration across internal and external stakeholders.
Pour le compte d'un acteur reconnu dans le domaine des systèmes d'information dédiés au secteur de la santé, nous recherchons un Ingénieur Intégration.L'environnement est composé de systèmes critiques, distribués sur de nombreux sites, utilisés par plusieurs milliers d'utilisateurs. Le poste s'inscrit dans une démarche de transformation et de modernisation continue du système d'information.
This position owns the technical interpretation and implementation of trading risk logic, with primary hands-on responsibility for SQL-based risk calculations and data layers. The role leads development across SQL, data ingestion, and frontend/backend streams, ensuring that positions, exposures, pricing, and P&L outputs are accurate, performant, and aligned with agreed business definitions.
Business Process and Operations Officer (M/F) - International Organization
This role is responsible for ensuring quality oversight of internal and external GxP activities within a global environment. Acting as a key cross-functional partner, you will collaborate with Quality, Supply Chain, Manufacturing, Clinical Operations, and Regulatory teams to ensure compliance and continuous improvement across the value chain.
The Pharmacovigilance (PV) Expert (a) will play a key role in ensuring compliance with pharmacovigilance processes and regulations within a biotech company. This temporary position requires a detail-oriented individual who can manage safety data and contribute to the overall safety of pharmaceutical products. Remote work possible but must be based in Switzerland. Start ASAP (latest July) for the next 12 months.
Rattaché au Responsable Validation et Métrologie, vous assurez la qualification et validation des équipements, procédés et systèmes. Vous intervenez sur l'ensemble du cycle de vie des activités de validation dans un cadre réglementaire exigeant.
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