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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.
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.
Rattaché au Responsable Validation et Métrologie, vous assurez la qualification et validation des équipements, procédés et systèmes. Vous intervenez sur l'ensemble du cycle de vie des activités de validation dans un cadre réglementaire exigeant.
This is a senior administrative and coordination role, supporting the leadership of a key control function. The position requires a proactive, highly organised professional who can operate confidently in an international and fast-paced environment, ensuring smooth day-to-day operations and high-quality stakeholder interaction.
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.
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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