regulatory Jobs in Basel

ul liInternational tätiges Unternehmen mit starkem Wachstumskurs /li liStart: Sofort/Vereinbantragung | Hybridmodell | Attraktive Vergütung Benefits /li /ul h3About Our Client /h3 pUnser Kunde ist ein erfolgreiches und schnell wachsendes Einzelhandelsunternehmen mit einer starken Filialpräsenz in ganz Europa. Im Rahmen einer ambitionierten...

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...

ulliInternational tätiges Unternehmen mit starkem Wachstumskurs /liliStart: Sofort/Vereinbanbarung| Hybridmodell | Attraktive Vergütung Benefits /li /ulh3Firmenprofil /h3pUnser Kunde ist ein erfolgreiches und schnell wachsendes Einzelhandelsunternehmen mit einer starken Filialpräsenz in ganz Europa. Im Rahmen einer ambitionierten Expansionsstrategie baut...

pRevolution 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...

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...

pNonStop Consulting AG is seeking a Global Head of Regulatory Strategy to shape and drive regulatory direction across an international pharmaceutical portfolio from Basel. This senior role combines strategic oversight with hands-on leadership of an experienced global team, influencing critical development and commercial decisions. /ppYou will collaborate...

International tätiges Unternehmen mit starkem WachstumskursStart: Sofort/Vereinbanbarung| Hybridmodell | Attraktive Vergütung & BenefitsFirmenprofilUnser Kunde ist ein erfolgreiches und schnell wachsendes Einzelhandelsunternehmen mit einer starken Filialpräsenz in ganz Europa. Im Rahmen einer ambitionierten Expansionsstrategie baut das Unternehmen seine...

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...

pRevolution Medicines, Inc. is seeking a Director, Regulatory Affairs, Switzerland, to lead regulatory activities and strategy for Swiss projects in alignment with Swissmedic and ICH guidelines. /ppYou will collaborate with medical, clinical, marketing and global RA teams to support lifecycle management, submissions, and compliance across regions. The role...

h3bGlobal Head of Regulatory Strategy /b /h3 pNonStop Consulting is partnering with an established international pharmaceutical organisation to appoint a Global Head of Regulatory Strategy. /p pThis is a high-impact senior leadership opportunity for an accomplished Regulatory Affairs executive to shape and drive global regulatory strategy across an...

pHeadcount 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. /ppThe...

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...

pF. Hoffmann-La Roche AG in Basel is launching a two-year One Product Development Regulatory (PDR) Early Talent Program. It provides foundational regulatory experience through hands-on assignments, with mentorship and learning solutions across therapeutic areas. /ppEarly exposure includes Health Authority interactions and regulatory document preparation,...

h3Innovative Biopharmaceutical Company | Northwestern Switzerland /h3 h3Build and Lead Internal Regulatory Affairs Capabilities for Late-Stage Development and NDA Filing. /h3 pOur client is an innovative, research-driven biotechnology company advancing a portfolio of novel small molecule therapies through late-stage clinical development. /p pAs the lead...

Aequor Consulting GmbH is seeking a technically skilled professional with proven experience in TRD Composer, regulatory documentation, and pharmaceutical data management. This role focuses on integrating and advancing regulatory IT systems while coordinating data governance in a highly regulated environment.The ideal candidate will coordinate data governance...

pMonte 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. /ppYou will drive Module 3 content, quality...

pParexel 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. /ppThe role...

pSkilled – Recruitment Solutions GmbH is seeking a Senior Documentation Quality Specialist to ensure rigor across clinical, nonclinical, and regulatory documents within global development programs. The role emphasizes clarity, regulatory compliance, and governance of templates and standards. /ppThe ideal candidate has a Master’s degree in life sciences...

pMonte Rosa Therapeutics, Inc. is seeking an Associate Director of CMC Regulatory Affairs to lead global regulatory strategy for Chemistry, Manufacturing and Controls. /ppYou will author Module 3 submissions, coordinate with Process Chemistry, Analytical Development, Drug Product, Quality, and Clinical Supply teams, and represent CMC in health authority...

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...