regulatory Jobs in Basel

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...

Möchten Sie das regulatorische Meldewesen für eine etablierte Basler Privatbank verantworten - dort, wo Zahlen, Aufsichtsrecht und Bankbetrieb zusammenkommen?Dann sind Sie bei E. Gutzwiller & Cie, Banquiers am richtigen Ort!Wir sind eine unabhängige Privatbank mit Fokus auf Vermögensverwaltung und individuelle Kundenbetreuung. Als Teil unseres Finance...

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...

Revolution 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.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...

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...

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...

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...

Overview We are looking for a senior Veeva Vault RIM specialist with strong pharmaceutical regulatory technology experience to provide independent advisory support for a major regulatory transformation programme. The consultant will assess implementation approaches, dependencies, risks and key technology decisions associated with Veeva Vault RIM and the...

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...

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...

CTC Resourcing Solutions AG client in Switzerland seeks a Senior Regulatory Affairs Documentation Specialist for a 2-year contract in the Basel area. The role focuses on ensuring submission-ready clinical, nonclinical, and regulatory documents across NDA/MAA/IND programs.The ideal candidate has Swiss work permit, a Master’s degree in a science field, 10+...

Monte Rosa Therapeutics seeks a seasoned Associate Director of CMC Regulatory Affairs to shape global CMC strategy and author critical submission content. You will collaborate with Process Chemistry, Analytical Development, Drug Product, Quality, and Clinical Supply to ensure compliant, high-quality filings.You will drive Module 3 content, quality summaries,...

Senior Regulatory Transformation / Programme Advisory Lead Basel, Switzerland | Posted on 09/25/2026 Industry Pharma/Biotech/Clinical Research Date Opened 09/25/2026 City Basel Job Posting ID ZR_4453_JOB What is the mission about? See JD Job Description Overview We are looking for a senior Regulatory Transformation /Programme Advisory professional to...

Veeva Vault RIM / Regulatory Technology SMEBasel, Switzerland | Posted on 09/25/2026We are looking for a senior Veeva Vault RIM specialist withstrong pharmaceutical regulatory technology experience to provide independentadvisory support for a major regulatory transformation programme.The consultant will assess implementation approaches,dependencies, risks...

Zohorecruit in Basel, Switzerland seeks a Senior Regulatory Transformation / Programme Advisory Lead to support a major pharmaceutical regulatory transformation programme involving Veeva Vault RIM, data migration, validation and release readiness. This advisory role delivers independent assessments and decision-support materials to senior stakeholders,...

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...