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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.
As CMC Program Manager, you will play a key role in driving the Chemistry, Manufacturing, and Controls (CMC) strategy and execution for the company's lead biologic program. You will collaborate closely with external Contract Development & Manufacturing Organizations (CDMOs) to ensure robust, cGMP-compliant process development and manufacturing to support upcoming clinical trials.
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.
Nous recherchons un(e) Legal Counsel pour renforcer l'équipe juridique dans le cadre d'un remplacement temporaire (c. 9 mois). Vous jouerez un rôle clé dans le soutien aux opérations commerciales, en particulier sur les contrats commerciaux et de distribution, tout en contribuant à la conformité réglementaire et à la protection des données.
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.
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 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.
Join our team as a Clinical Operations Coordinator and play a key role in supporting the operational management of global clinical trials from start-up to archiving
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.)
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 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.
Für eine etablierte, interdisziplinäre Gesundheitsorganisation in der Schweiz, die in einem dynamischen und regulierten Umfeld tätig ist, suchen wir eine/n Senior HR Generalist / HR Business Partner (m/w). Die Organisation zeichnet sich durch Wachstum, laufende Transformationen sowie einen starken Fokus auf Qualität, Compliance und Mitarbeitende aus.
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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