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As Medical Director, you will ensure 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.
Our client is seeking a Senior Quality Technician responsible for executing quality control activities and ensuring compliance with quality and regulatory standards. This role supports the development, inspection, and maintenance of high‑quality medical device products within an innovative and dynamic organisation.
The Laboratory Technician (Analytical Chemistry) performs analytical testing of biologics for release, stability, and characterization in a GMP-regulated environment. The role includes working with techniques such as HPLC/UPLC, supporting method validation and transfers, and documenting results according to cGMP standards. The position also involves troubleshooting methods and supporting equipment maintenance.
Our client is seeking a consultant to support both the Industrial Process Support Team and the Product Development Team during a period of increased industrial activity. The consultant will contribute to developing, securing, and transferring key manufacturing and sterilisation processes while strengthening technical documentation and supporting cross‑functional operations.
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.
The Integration Programme Manager (PMO) supports the Integration Manager in planning, coordinating, and executing the integration of acquired organisations across Switzerland.
As a Quality Specialist, you are responsible for ensuring product-related quality across the entire value chain. You act as a central coordination point between international teams and drive continuous quality improvement.
The Integration Manager is responsible for leading and executing the end-to-end integration of acquired companies into the broader organization, ensuring the realization of strategic objectives, synergies, and financial targets.
Our client is looking for a Process Engineer who will lead technical studies and develop effective process solutions across early‑stage engineering phases. The role ensures safe, reliable, and optimized operations by applying best practices, standards, and rigorous process engineering methods.
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.
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