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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.
Vous pilotez l'amélioration continue et la performance des lignes de production au sein d'un environnement industriel complexe. Vous accompagnez les équipes dans la standardisation des processus, la mise en place d'indicateurs de performance et le déploiement des méthodologies Lean.
Our client is a prestigious international organization headquartered in Basel. To support its Strategic Programme Office (SPMO), they are looking for a PMO Specialist who will play a key role in governance, reporting, and programme coordination activities. This position offers exposure to strategic initiatives, senior stakeholders, and a highly collaborative international environment.
The Senior Clinical Trial Assistant provides essential operational and administrative support across all phases of clinical studies. This role ensures high-quality documentation, compliance with regulatory standards, and smooth collaboration across internal and external stakeholders.
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.
Our client is looking for a Quality Operations Technician to ensure products manufactured by external suppliers and contract manufacturers consistently meet quality, regulatory, and business requirements. The role combines operational quality oversight, supplier collaboration, batch release activities, and continuous improvement within a highly regulated medical technology environment.
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