Jobs für regulatory project bei Basel

## 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...

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....

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...

The Position As a Regulatory Innovation & Sustainment Leader in the Pharmaceutical Development Regulatory (PDR) Innovation & Sustainment chapter, you will drive the digital transformation of regulatory workflows, specifically focusing on AI and data strategy. You will bridge the gap between business needs and technical execution, fostering a culture of...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Home Based position requiring German language...

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...

bOverview /b pYou lead QA-driven, global projects that bring life-changing therapies to market. You provide strategic QA guidance across development teams, ensuring cGMP compliance and high-quality deliverables. You drive inspection readiness and regulator-facing activities, shaping submissions and third-party contracts. This role combines cross-functional...

Be a hero for our rare disease patientsAt 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 won’t go – challenging...

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...

ppDescription /p h3JOB SUMMARY /h3 pThe Global Project Manager (GPM) oversees, leads, and coordinates the cross-functional operational aspects of ongoing global and multi-regional clinical projects to ensure that the clients' goals of time, cost, and quality are met from protocol concept to final clinical study report. This role focuses specifically on...

IQVIA is seeking a Site Activation professional to manage country-level site activation activities (SA) and related regulatory/document tasks. The role emphasizes working under SOPs, WIs, and project timelines, with focus on accuracy of regulatory materials and timely site activation.Requirements include a Bachelor’s degree in life sciences and at least 3...

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...

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...

A global leader in innovative solutions is seeking a Regulatory Affair Specialist in the United Kingdom. This role involves leading regulatory strategy and managing product registrations, particularly in Hygiene and Home Care sectors. Candidates should have a PhD or a degree in natural sciences, with 5-10 years of relevant industry experience. Strong...

GXP CONSULTING Switzerland is a Swiss company made up of a passionate team of life-science professionals. Since 2014, we have been providing our clients with cutting-edge expertise and support covering the entire product life cycle. Join a team where your skills will have a real impact on patients’ lives. We are looking for an Engineering Project Manager...

Job Title: MSAT Technical Lead (DS Biologics)Location: Switzerland or RemoteDuration: ASAP until 31 December 2026FTE: 100%Travel: Up to 30%Our client is seeking an experienced MSAT Technical Lead with deep expertise in Drug Substance (DS) Biologics manufacturing to support commercial and clinical biologics operations. The successful consultant will provide...

Clinilabs in Basel, Switzerland seeks a Study Start-up Lead (SSUL) to oversee regulatory submissions for clinical trials globally or regionally, ensuring startup deliverables and timelines. You will provide strategic submission planning and cross-functional coordination, mentoring junior team members while working under regulatory requirements and company...

bOverview /b pAs a DMPK-PD Project Leader at Roche pRED, you steer nonclinical and translational programs to deliver the right drug at the right dose. You lead cross-functional efforts across discovery to clinic, shaping translational strategies and PK/PD concepts. You apply modelling, PBPK and regulatory insight to de-risk programs and enable patient access...

Alentis Therapeutics, the Claudin-1 Company, is on a mission to treat cancer and reverse fibrosis.To this end, we are rapidly advancing a clinical pipeline of anti-Claudin-1 monoclonal antibodies. Every day, we get opportunities to make a positive impact – on our colleagues, partners, customers and society.Together, we’re pioneering the solutions of the...