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- For our client, a leading biotechnology company based in canton Zug, we are seeking a Regulatory Affairs Manager. General Information: Start date: ASAPEnd date: 30/06/2026Contract: temporary contract via RandstadWorkplace: Baar, ZugWorkload: 100%Working hours: StandardTask & Responsibilities: Responsible for managing the development and implementation of regulatory strategy for specific projects and programs. Contribute to identification and assessment ofFor our client, a leading biotechnology company based in canton Zug, we are seeking a Regulatory Affairs Manager. General Information: Start date: ASAPEnd date: 30/06/2026Contract: temporary contract via RandstadWorkplace: Baar, ZugWorkload: 100%Working hours: StandardTask & Responsibilities: Responsible for managing the development and implementation of regulatory strategy for specific projects and programs. Contribute to identification and assessment of
- For our client in Rotkreuz, a major player in the pharmaceutical sector, we are looking for an experienced and motivated Sourcing Manager. In this role, you will be responsible for managing procurement activities, ensuring compliance with internal policies, and building strong partnerships with suppliers and stakeholders.Your Responsibilities:Manage procurement requests in line with category strategies, company policies, and supplier agreementsCollaborateFor our client in Rotkreuz, a major player in the pharmaceutical sector, we are looking for an experienced and motivated Sourcing Manager. In this role, you will be responsible for managing procurement activities, ensuring compliance with internal policies, and building strong partnerships with suppliers and stakeholders.Your Responsibilities:Manage procurement requests in line with category strategies, company policies, and supplier agreementsCollaborate
- For one of our clients, a world leader in in-vitro diagnostics, we are currently looking for a Product Safety Specialist - Electronic Diagnostics Instruments.General Information: Start date: asapLatest possible start date: 01.02.2026Duration: 1 year with the possibility of extensionWorkplace: Rotkreuz Workload: 80-100%Remote/Home Office: possible, at least 3 days on site work per week is expectedWorking hours: StandardDepartment: Compliance Operations,For one of our clients, a world leader in in-vitro diagnostics, we are currently looking for a Product Safety Specialist - Electronic Diagnostics Instruments.General Information: Start date: asapLatest possible start date: 01.02.2026Duration: 1 year with the possibility of extensionWorkplace: Rotkreuz Workload: 80-100%Remote/Home Office: possible, at least 3 days on site work per week is expectedWorking hours: StandardDepartment: Compliance Operations,
- We are looking for a full stack software engineer to strengthen our software team within. This is a hands-on software development position where you define, build, test and release high-quality software. As a domain expert, you will have a large influence on projects to enhance our future product portfolio.Tasks & Responsibilities:You develop concepts and participate in feasibility studies to meet technical requirements.You perform and take ownership ofWe are looking for a full stack software engineer to strengthen our software team within. This is a hands-on software development position where you define, build, test and release high-quality software. As a domain expert, you will have a large influence on projects to enhance our future product portfolio.Tasks & Responsibilities:You develop concepts and participate in feasibility studies to meet technical requirements.You perform and take ownership of
- Do you have a passion for DevOps and automation in a medically regulated environment? We are looking for an experienced engineer to build and maintain our CI/CD pipelines, ensuring the timely delivery of stable, secure, and scalable systems that meet crucial customer and patient needs.General Information:Start date: asaplatest Start Date: 01.12.2025Planned duration: 31.12.2026Extension: very likelyWorkload: 80% - 100%Home Office: possibleTeam: 13Do you have a passion for DevOps and automation in a medically regulated environment? We are looking for an experienced engineer to build and maintain our CI/CD pipelines, ensuring the timely delivery of stable, secure, and scalable systems that meet crucial customer and patient needs.General Information:Start date: asaplatest Start Date: 01.12.2025Planned duration: 31.12.2026Extension: very likelyWorkload: 80% - 100%Home Office: possibleTeam: 13
