regulatory affairs associate Jobs in Basel

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...

OverviewMonte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of CMC Regulatory Affairs. The CMC Regulatory Affairs will serve as a key regulatory strategist and author for the Chemistry, Manufacturing, and Controls components of Monte Rosa's global regulatory filings. This...

Overview Monte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of CMC Regulatory Affairs. The CMC Regulatory Affairs will serve as a key regulatory strategist and author for the Chemistry, Manufacturing, and Controls components of Monte Rosa's global regulatory...

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...

Innovative Produkte hautnah - Region BaselUnser 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 klinisch in...

Monte Rosa Therapeutics, Inc is seeking an Associate Director of CMC Regulatory Affairs to lead global regulatory strategies for Chemistry, Manufacturing, and Controls across development stages. You will author Module 3 content, review summaries, and partner with Process Chemistry, Analytical Development, Drug Product, Quality, and Clinical Supply teams to...

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...

OverviewMonte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of CMC Regulatory Affairs. The CMC Regulatory Affairs will serve as a key regulatory strategist and author for the Chemistry, Manufacturing, and Controls components of Monte Rosa's global regulatory filings. This...

Lonza in Visp, Switzerland, seeks an experienced Manager Regulatory Affairs to lead end-to-end regulatory programs at the manufacturing site. You will shape regulatory strategies, coordinate cross-functional teams, and ensure timely delivery for complex projects, including health authority interactions and lifecycle activities.The role requires a strong...

Senior Regulatory Affairs Documentation Specialist – 7103 Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking for an experienced Senior Regulatory Affairs Documentation Specialist to act as a...

Location: the actual location of this job is in Visp, Basel, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. This is a temporary position for a period of one year. As a Manager Regulatory Affairs based at our manufacturing site in Visp , you provide end-to-end regulatory leadership for complex client...

Revolution Medicines seeks an Associate Director, Regulatory Affairs, Europe to provide strategic regulatory leadership for designated oncology programs across Europe, the EU/EEA, UK and Switzerland. You will align regulatory plans with global goals and drive end-to-end MAA filings while engaging with EMA, MHRA and Swissmedic.You will lead cross‑functional...

Parexel International seeks an experienced Regulatory Affairs Consultant to join our global Regulatory Affairs team in Basel, working from the office 2 days a week. You will develop, review, and manage regulatory submissions and compliance across product lifecycles, collaborating with cross-functional teams and applying independent judgment.The role entails...

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...

pCTC Resourcing Solutions AG is seeking a Regulatory Affairs Consultant for a 6-month contract in Rotkreuz, Switzerland. Fluent German speakers with a degree in medical technology, natural sciences, or industrial engineering and at least 3 years in regulatory affairs or quality management in the medtech/IVD sector are preferred. /ppThe role involves...

ph3Regulatory Affairs Consultant – Swiss MepV/IvDV – 7107 URA /h3 pOur client is a leading Swiss multinational healthcare company headquartered in Basel, Switzerland. Operating in Pharmaceuticals and Diagnostics, it is one of the world’s largest biotech companies and a global leader in in-vitro diagnostics and cancer treatments. Our client is known for...

Senior Manager / Associate Director, Regulatory Strategy - CMC Location: Basel Monte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our teams. This role will focus on oncology, immunology, and related therapeutic areas. The successful candidate will be responsible for developing and implementing regulatory...

We are seeking an experienced Regulatory Affairs Consultant to join our global Regulatory Affairs team. In this role, you will develop, review, and manage regulatory submissions and compliance activities for pharmaceutical products throughout their lifecycle—from clinical development through post-market activities. You will work collaboratively with...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...

Monte Rosa Therapeutics is seeking an Associate Director of CMC Regulatory Affairs to lead global regulatory strategy for Chemistry, Manufacturing, and Controls across development stages. You will author and review Module 3, coordinate with Process Chemistry, Analytical Development, Drug Product, Quality, and Clinical Supply teams, and interact with health...