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In this role, you lead quality investigations and CAPA processes to ensure product and process compliance. You play a key role in continuous improvement and proactive resolution of quality issues.
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.
Our client is seeking afull-time Laboratory Technician for a 6 to 12‑month assignment to support a scientific research initiative. The role focuses on retrieving, organizing, and preparing a very large number of tissue samples for international shipment, ensuring full traceability and data accuracy.
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.
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.
The Data Analytics Specialist is responsible for designing, developing, and operating the analytics layer of the organisation's enterprise data platform, hosted on Oracle Cloud Infrastructure (OCI). The role focuses on transforming operational data into trusted analytical datasets, dashboards, and reusable data assets that enable self‑service reporting and data‑driven decision‑making.
We are supporting a well-established and innovative international company in the medical devices sector in the search for a Quality & Compliance sr. Director. This is a key leadership role within a highly regulated, manufacturing-driven environment, offering strong strategic and operational exposure.
Our client is seeking a Pharmaceutical Quality Assurance Specialist to ensure the procurement of safe, effective, and high-quality health products. You will play a key role in policy development, risk management, and cross-functional collaboration within a global supply environment.
The (Senior) Manager REGULATORY AFFAIRS (a) will play a pivotal role in ensuring compliance with industry standards and regulatory requirements. Depending on the experience level of the candidate, this temporary position in Basel involves supporting/leading regulatory processes with national authorities in CH. Start is ASAP latest in July till end of the year. Remote work possible however the candidate has to be located in Switzerland. Extension is possible.
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