Jobs für regulatory bei Basel

pRoche is seeking a Group Director in Pharma Technical Regulatory (PTR) to lead end-to-end regulatory strategies across product portfolios on a global scale. You will advocate, drive changes, and align resources with leaders to deliver outcomes that matter for patients and stakeholders. /ppYou will oversee health authority interactions, build...

ppBei Roche kannst du ganz du selbst sein und wirst für deine einzigartigen Qualitäten geschätzt. Unsere Kultur fördert persönlichen Ausdruck, offenen Dialog und echte Verbindungen. Hier wirst du für das, was du bist, wertgeschätzt, akzeptiert und respektiert. Dies schafft ein Umfeld, in dem du sowohl persönlich als auch beruflich wachsen kannst....

ph3Innovative Produkte hautnah - Region Basel /h3pUnser Kunde ist ein pharmazeutisches Familienunternehmen in der Health Care Branche im Grossraum Basel. Der Hauptsitz und Standort in der Schweiz forscht, entwickelt und produziert ein hochwertiges Produkteportfolio. Davon zählen einige Präparate in der Schweiz zu den Marktführern. Die Produkte werden...

## Senior Regulatory Group DirectorApplylocations: Baseltime type: Full timeposted on: Posted Todayjob requisition id: At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,...

ppAt Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure...

Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target...

Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target...

**Ihr Aufgabengebiet**: - Sicherstellung der Einhaltung von regulatorischen Anforderungen für die Entwicklung, Herstellung und Markteinführung von Medizinprodukten - Pflege und Aktualisierung regulatorischer Dokumentationen zur Sicherstellung der Compliance - Ansprechpartner für Behörden/Agenturen für die Produktezulassung - Fachliche Unterstützung...

Arxada is a global leader in innovative solutions that protect our world. Our groundbreaking technologies, in-depth regulatory know-how, manufacturing and process development help our customers to safeguard nutrition, health and infrastructure efficiently through chemistry and biotechnology that enhance sustainability. We offer a broad portfolio of...

pRoche Holding AG in Basel sucht eine visionäre Führungspersönlichkeit im PTR-Umfeld, die regulatorische Strategien auf Portfolioebene entwickelt und umsetzt. In dieser Rolle tragen Sie die Verantwortung für Prioritäten, Ressourcenplanung und die Ausrichtung über Funktionsbereiche hinweg. /ppSie fördern selbstverwaltete Teams, unterstützen...

Wir suchen einen Group Manager Regulatory Affairs, der unsere globale regulatorische Strategie verantwortet, ein Team führt, die Einhaltung aller Anforderungen sicherstellt und effiziente Prozesse in einem dynamischen, internationalen Umfeld vorantreibt. Group Manager Regulatory Affairs 100% Ihr Aufgabengebiet Fachliche und disziplinarische Führung...

pRevolution Medicines is seeking an experienced Principal Regulatory Medical Writer to lead the preparation of regulatory documentation for clinical development and marketing authorization across Europe. You will collaborate with Regulatory Affairs, Clinical Development, and cross-functional teams to author, coordinate and finalize submissions. /ppThe role...

Why Join Us?   Be a hero for our rare disease patients   At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to do. To achieve this goal, our vision is to lead the future of rare disease medicine. For us, this means going where other biopharma companies...

pClinilabs seeks a Vice President of Quality Assurance to lead the quality and regulatory teams, shaping strategy for quality systems and compliant operations across clinical trials. You will ensure cGCP adherence, regulatory readiness, and harmonization of processes within the organization. /ppThis role requires deep GXP experience, strong leadership, and...

pgloorlang AG in Basel seeks a senior Regulatory Affairs CMC expert to lead global CMC strategy for development and registration of small molecule therapies, shaping regulatory submissions (Module 3) and lifecycle management in collaboration with CMC Development, Analytical Development, Manufacturing and Quality. /ppYou will guide IND, NDA and MAA...

Ein pharmazeutisches Familienunternehmen in der Region Basel sucht einen Experten für die Erstellung von Swissmedic Zulassungsanträgen. Die Rolle erfordert eine langjährige Erfahrung in der Arzneimittelzulassung sowie einen naturwissenschaftlichen Abschluss. Favorisiert werden Kenntnisse im Bereich Dermokosmetika. Deutsch als Muttersprache und...

ppDescription /p h3JOB SUMMARY /h3 pThe Vice President of Quality Assurance is responsible to implement and support strategies for Quality System processes and supporting technology, and ensuring the integrity, consistency, and harmonization of these processes and systems for Clinilabs. /p pThis individual is also accountable for ensuring that the clinical...

Roche Basel is offering an internship in Environmental Regulatory Affairs where you will work with Regulatory Experts to navigate global chemical policies and support compliance for life-saving products. You will gather data for registration dossiers, monitor external studies, and help implement a global compliance tool under senior guidance.The role...

Headcount is seeking a Director of Regulatory Affairs CMC Europe to lead the regulatory strategy for novel small-molecule therapies in oncology. This role requires steering global CMC development, submissions and lifecycle management across clinical, regulatory and manufacturing functions, with a focus on Module 3 and interactions with FDA/EMA.The candidate...

ph3Who We Are: /h3pAt Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs. /ph3What We Do: /h3pNeurocrine Biosciencesis a...