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Die Position verbindet klinische Unterstützung im Operationssaal mit technischer Expertise in der orthopädischen Implantologie. Sie umfasst die enge Zusammenarbeit mit chirurgischen Teams sowie die operative und organisatorische Betreuung komplexer Fälle.
The role is responsible for managing and maintaining the Quality Management Systems (QMS) across multiple sites, including the handling of deviations, CAPAs, and change records, while ensuring full compliance with GMP and regulatory requirements within a pharmaceutical environment. It supports the improvement and harmonization of global QMS processes and plays a key role in inspection readiness activities and internal audits.
For our client, an international biotech company with modern offices in Lucerne area, we are looking for a Manufacturing Technology Innovation Specialist (a), who will play a key role in optimizing and maintaining production processes. The temporary contract will start in March for a duration of 24 months with extension option.PLEASE NOTE: This function requires 100% onsite presence.
As Senior Legal & Compliance Counsel for the DACH region, you will provide expert legal advice and ensure compliance across Switzerland, Germany, and Austria. This is a strategic role with exposure to complex commercial and regulatory matters in the healthcare sector.
As Medical Director, you will shape and lead the medical strategy across the portfolio, ensuring scientific excellence, regulatory compliance and strong collaboration with commercial teams. You will act as the primary medical expert internally and externally, while maintaining close relationships with key opinion leaders, medical societies and healthcare professionals across Switzerland.
For our client, a globally renowned pharmaceutical company in the Basel area, we are seeking a Technical Regulatory Affairs CMC (Associate Director) to strengthen the team in 2026 in support of Phase 3 development activities. The contract duration is 12-24 months.Depending on the selected candidate's performance and motivation, the possibility of an extension or a permanent take over.
For our client, a globally renowned pharmaceutical company in the Basel area, we are seeking a Regulatory Affairs CMC professional to strengthen the team in 2026 in support of Phase 3 development activities. The contract duration is 12-24 months and is open to candidates with 5+ years of relevant experience across different seniority levels.
For our client, a globally renowned pharmaceutical company in the Basel area, we are seeking a Clinical Operations Manager (a) to strengthen the team in 2026 in support of Phase 3 development activities (cardiovascular combination product). The contract duration is 12-24 months with a strong take-over possibility.Hybrid work model: 3 days onsite, 2 days HO.
For our client, a globally renowned pharmaceutical company in the Basel area, we are seeking a Clinical Data Manager (a) to strengthen the team in 2026 in support of Phase 3 development activities. The contract duration is 24 months with a strong take-over possibility.Hybrid work model (3 days onsite, 2 days HO.)
We are looking for a Legal Counsel, available immediately, to temporarily strengthen a legal team. The candidate will provide operational support in the day‑to‑day management of legal and compliance matters in a dynamic and challenging environment. One‑month assignment, with potential extension to be discussed.
For our client, a globally renowned pharmaceutical company in the Basel area, we are seeking an experienced, hands-on Clinical Trial Physician (a) to support an active clinical development program (cardiovascular diseases). Hybrid work model (3 days onsite, 2 days home office). The start is latest in March for the next 12 months.
For our client, a globally renowned pharmaceutical company in the Basel area, we are seeking a Clinical Operations professionals to strengthen the team in 2026 in support of Phase 3 development activities. The contract duration is 12-24 months and is open to candidates with 5+ years of relevant experience across different seniority levels.
For our client, a globally renowned pharmaceutical company in the Basel area, we are seeking a Quality Assurance (GMP&Clinical) professional to strengthen the team in 2026 in support of Phase 3 development activities. The contract duration is 12-24 months and is open to candidates with 5+ years of relevant experience across different seniority levels.
For a leading interdisciplinary healthcare company in Zurich, we are looking for an experienced HR Business Partner (m/f) who enjoys supporting people and organizations through growth and change. In this role, you will be the central point of contact for all HR topics along the employee life cycle and play a key role in driving the ongoing development of our organization.
En tant qu'INFIRMIÈRE CHEFFE ou INFIRMIER CHEF, COORDINATRICE/COORDINATEUR DE SITE dans le secteur de la SANTÉ, vous serez responsable de la gestion des équipes et de la coordination des activités sur le site. Ce poste permanent situé à Genève exige des compétences solides en organisation et en gestion.
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