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Our client is seeking a Pharmaceutical Quality Assurance Specialist to ensure the procurement of safe, effective, and high-quality health products. You will play a key role in policy development, risk management, and cross-functional collaboration within a global supply environment.
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.
The (Senior) Manager REGULATORY AFFAIRS (a) will play a pivotal role in ensuring compliance with industry standards and regulatory requirements. Depending on the experience level of the candidate, this temporary position in Basel involves supporting/leading regulatory processes with national authorities in CH. Start is ASAP latest in July till end of the year. Remote work possible however the candidate has to be located in Switzerland. Extension is possible.
In this role, you lead quality investigations and CAPA processes to ensure product and process compliance. You play a key role in continuous improvement and proactive resolution of quality issues.
Our client is seeking afull-time Laboratory Technician for a 6 to 12‑month assignment to support a scientific research initiative. The role focuses on retrieving, organizing, and preparing a very large number of tissue samples for international shipment, ensuring full traceability and data accuracy.
As a Senior Team Assistant you will play a key role in supporting senior management and ensuring the smooth operation of administrative tasks.
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.
En tant que SECRÉTAIRE MÉDICALE 100%, vous jouerez un rôle clé dans la gestion administrative des dossiers médicaux et l'assistance des professionnels de la santé. Ce poste temporaire est basé à Genève, dans le secteur de la SANTÉ.
We are seeking a Team Assistant to support a team of directors on a 3-month temporary assignment. This role is fully office-based and combines classic administrative support with office management responsibilities, ensuring the smooth day-to-day running of the team and workplace. The ideal candidate is detail-oriented, service-minded, and able to manage multiple priorities in a fast-paced environment.
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.
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