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Rattaché(e) au Responsable Maintenance, vous assurez la fiabilité et la performance des équipements de production dans un environnement pharmaceutique certifié. Vous intervenez sur l'ensemble du cycle de maintenance en respectant strictement les normes GMP et EHS.
Our client is seeking a junior-level Mechanical Drafter/Designer to support the clean-up, update, and preparation of technical drawings and documentation. This is an operational drafting position, focused on execution and quality.
As a Quality Control Technician, you will perform quality control activities on raw materials, bulk products, and utilities to ensure compliance with quality standards. You will actively contribute to investigations, documentation, and the continuous improvement of laboratory operations.
The Pharmacovigilance (PV) Expert (a) will play a key role in ensuring compliance with pharmacovigilance processes and regulations within a biotech company. This temporary position requires a detail-oriented individual who can manage safety data and contribute to the overall safety of pharmaceutical products. Remote work possible but must be based in Switzerland. Start ASAP (latest July) for the next 12 months.
This role is responsible for ensuring quality oversight of internal and external GxP activities within a global environment. Acting as a key cross-functional partner, you will collaborate with Quality, Supply Chain, Manufacturing, Clinical Operations, and Regulatory teams to ensure compliance and continuous improvement across the value chain.
Reporting to the R&D leadership team, the Beverage Technology Manager will play a key role in developing, scaling up, and industrializing innovative beverage solutions. This position combines laboratory and pilot plant activities with industrial implementation projects across multiple production sites worldwide.
For our client, a leading international pharmaceutical company with modern offices in the canton of Lucerne, we are seeking a Batch Record Review Specialist (m/f/d). In this role, you will support clinical biologics manufacturing by reviewing completed batch records and ensuring all documentation meets ALCOA+ and GMP standards.
We are looking for a Quality Manager to oversee and develop a harmonized Quality Management System across two production sites in a regulated MedTech environment. This role combines operational leadership, regulatory compliance, and strategic quality oversight with direct team management responsibilities.
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