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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.
For our client, a leading international pharmaceutical company with modern offices in the canton of Lucerne, we are currently seeking a Supplier Quality Specialist (m/f/d).In this role, the selected candidate will work closely with the site supply chain team, as well as local quality, technology transfer, procurement, and manufacturing operations, collaborating across cross-functional, self-directed teams within the site's value stream.
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, 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.
Our Client is seeking a Quality Manager to oversee the Swiss regulatory compliance and quality oversight for all products imported and exported through the Swiss entity. Although no production occurs locally, this role is critical for maintaining Swiss compliance, managing audits by Swissmedic, and enabling local market operations. The position will provide strategic quality leadership and has the potential to grow.
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.
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