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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.
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.
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.
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.
The Program Manager will lead complex strategic programs and projects across the division, from initiation to completion, ensuring delivery on time, cost, and quality. The role requires strong leadership, governance, and execution skills in a technical and international environment .
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.
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