Senior Regulatory Affairs: CMC
Vor 3 Tagen
A leading biotech firm in Zurich is seeking a Senior Expert in Regulatory Affairs to shape CMC regulatory strategies for complex biologics. This crucial role requires 7+ years of experience in Regulatory Affairs, knowledge of EMA and FDA procedures, and a background in biotechnology. The position offers competitive compensation and the opportunity to work on impactful biosimilar programs within a collaborative international environment.
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Senior Expert Regulatory Affairs
Vor 3 Tagen
Zürich, Schweiz gloor & lang consultants VollzeitSenior Expert Regulatory Affairs - CMC/Biosimilars Shape CMC regulatory strategy for complex biologics in a fast-growing biotech environment For a fast‑growing, internationally active biotech company focused on biosimilar development, we are currently looking for a Senior Expert Regulatory Affairs with a strong CMC focus. Workplace is Region Zug‑Zurich...
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Regulatory Affairs Professional
vor 2 Wochen
Zürich, Schweiz nemensis ag VollzeitOverviewNavigate Complex Regulatory Landscapes – Join Our Expert NetworkTalent Pool Registration: Building our Regulatory Affairs networkOpportunities: Permanent and temporary positions availableBuilding Our Regulatory Affairs Talent NetworkWe are actively building a comprehensive talent pool of Regulatory Affairs professionals for our diverse client...
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Regulatory Affairs Manager
Vor 5 Tagen
Zürich, Schweiz Takeda Pharmaceutical Vollzeit**People First** - At Takeda we are dedicated to improving the health and well-being of all people and bringing them the hope of a brighter future. It is our passion that transforms every job into meaningful action. **Our people are the heart of Takeda.** Our team is growing and for this we need bright minds with creativity and flexibility - what talent do...
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Associate Principal Scientist, Regulatory Affairs
vor 2 Wochen
Zürich, Schweiz MSD VollzeitWe are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for...
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GRA CMC Director
vor 1 Woche
Zürich, Schweiz Takeda VollzeitDescription – Director GRA CMC Marketed Products Development (MPD) LeadJoin Takeda as Director, Global Regulatory Affairs CMC Marketed Products Development (MPD) Lead, where you are accountable for developing and executing on GRA CMC strategies for lifecycle management. You develop and execute on global strategies across the existing portfolio, lead a...
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GRA CMC Director
vor 1 Woche
Zürich, Schweiz Takeda VollzeitDescription – Director GRA CMC Marketed Products Development (MPD) LeadJoin Takeda as Director, Global Regulatory Affairs CMC Marketed Products Development (MPD) Lead, where you are accountable for developing and executing on GRA CMC strategies for lifecycle management. You develop and execute on global strategies across the existing portfolio, lead a...
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Regulatory Affairs Manager
vor 2 Wochen
Zürich, Schweiz Proclinical VollzeitShape the future of vaccines-drive regulatory excellence across Europe. Proclinical is seeking a Regulatory Affairs Manager for a contract role based in Switzerland. This position focuses on supporting regulatory activities related to the development, registration, and lifecycle management of vaccine candidates in Europe. The role offers flexibility with...
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Zürich, Schweiz Takeda VollzeitCMC Senior Project Lead, Global Biologics Manufacturing Sciences Join Takeda as a CMC Senior Project Lead, Global Biologics Manufacturing Sciences (GMsci Bio) and play a pivotal role in advancing our biologics portfolio. You will provide project management expertise for strategic initiatives and Chemistry, Manufacturing and Controls (CMC) Life Cycle...
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Senior CMC Project Lead – Global Biologics
Vor 5 Tagen
Zürich, Schweiz TAKEDA PHARMACEUTICALS AMERICA, INC. VollzeitA leading global biopharmaceutical company in Zurich is seeking a CMC Senior Project Lead to oversee biologics manufacturing. This role involves co-leading CMC project teams, ensuring compliance with lifecycle management strategies, and making data-driven decisions. The ideal candidate will have a BS/MS in engineering or life sciences, at least 5 years of...
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Leiter:in Quality Management
vor 1 Woche
Zürich, Schweiz CISTEC AG VollzeitLeiter:in Quality Management & Regulatory Affairs (80 – 100%) Die CISTEC AG ist ein erfolgreiches KMU und sucht laufend qualifizierte und motivierte Mitarbeiter: innen. Wenn du Interesse hast, bei einem innovativen Software- und Dienstleistungsunternehmen im Gesundheitswesen tätig zu sein, melde dich bei uns. Aufgrund unseres Wachstums suchen wir für...