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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.
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.
Our client is a prestigious international organization headquartered in Basel. To support its Strategic Programme Office (SPMO), they are looking for a PMO Specialist who will play a key role in governance, reporting, and programme coordination activities. This position offers exposure to strategic initiatives, senior stakeholders, and a highly collaborative international environment.
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.
Nous recherchons un Ingénieur Qualité pour piloter et améliorer la conformité et la fiabilité des produits tout au long de la chaîne de production. Ce rôle implique une forte dimension opérationnelle et transverse, avec la gestion des non-conformités, l'animation de démarches qualité et le déploiement de méthodologies d'amélioration continue.
Vous pilotez l'amélioration continue et la performance des lignes de production au sein d'un environnement industriel complexe. Vous accompagnez les équipes dans la standardisation des processus, la mise en place d'indicateurs de performance et le déploiement des méthodologies Lean.
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.
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