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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.
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.
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.
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.
Nous recherchons un Ingénieur Qualité pour piloter et améliorer la conformité et la fiabilité des produits tout au long de la chaîne de production. Ce rôle implique une forte dimension opérationnelle et transverse, avec la gestion des non-conformités, l'animation de démarches qualité et le déploiement de méthodologies d'amélioration continue.
The CQV ENGINEER (a) will play a key role in overseeing the commissioning, qualification, and validation activities for systems and equipment in the LIFE SCIENCE sector. Based in Lucerne, this temporary position (18 months contract) offers an exciting opportunity to contribute to high-quality standards in a dynamic and regulated environment. Start is in July.
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