regulatory genome development Jobs in Basel

pRoche is offering a two-year Early Talent program in Regulatory Affairs that blends hands-on assignments with tailored learning. It provides exposure to the full lifecycle of pharmaceutical products and rotating opportunities within PDR. /ppETs work with global teams, developing scientific writing skills and preparing regulatory documents for Health...

pAt 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...

pAt 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...

Bei 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....

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...

NonStop 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.You will collaborate closely...

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 Biopharmaceutical Company | Northwestern Switzerland Build and Lead Internal Regulatory Affairs Capabilities for Late-Stage Development and NDA Filing. Our client is an innovative, research-driven biotechnology company advancing a portfolio of novel small molecule therapies through late-stage clinical development. As the lead program approaches a...

Global Head of Regulatory Strategy NonStop Consulting is partnering with an established international pharmaceutical organisation to appoint a Global Head of Regulatory Strategy. This is a high-impact senior leadership opportunity for an accomplished Regulatory Affairs executive to shape and drive global regulatory strategy across an international...

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...

ppSelect how often (in days) to receive an alert: /p pThe purpose of Idorsia is to challenge accepted medical paradigms, answering the questions that matter most. To achieve this, we will discover, develop, and commercialize transformative medicines – either with in-house capabilities or together with partners – and evolve Idorsia into a leading...

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,...

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...

If you have hands-on laboratory experience on biomarker assays with special focus on ligand binding assays, this role might be perfect for you! Our client is looking for a Biomarker Development Scientist to execute exploratory biomarker strategies across their clinical pipeline, and deliver innovative biomarker solutions. Responsibilities Hands-on...

Roche seeks a Principal Regulatory Program Director to architect and drive global regulatory strategy for complex drug-device technologies. You will integrate device and pharma regulatory domains, shaping policy while aligning with Roche's strategic objectives.The role emphasizes leadership, cross-functional collaboration, and stakeholder engagement to...

Roche Pharma in Basel seeks a Principal Regulatory Program Director to turn regulatory complexity into strategic advantage across portfolio delivery and global policy shaping. You will steward device and CMC regulatory frameworks with PK/BE bridging knowledge and drive cross-disciplinary execution.You will shape global regulatory strategy for drug-device...

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

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 filings. This individual...

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,...