Regulatory Submissions Jobs in Switzerland
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Manager Sr. Manager – Quality Gmp
Monte Rosa Therapeutics
OverviewThe Manager GMP Quality is responsible for the oversight and day-to-day quality interface with CDMO producing DS & DP for MRTxs ongoing clinical programs.. This includes supporting the review of MBRs/EBRs analytical methods validation protocols/reports specifications release data packages an...
Scientist, Pharmaceutical Development & Data Analy...
Roche
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 allowing you to thrive both personally and professionally. This is how we aim...
Global Program Safety Team Lead
Novartis
BandLevel 7Job Description SummaryStep into a career-defining opportunity where your leadership can transform patient outcomes on a global scale! As our Global Program Safety Team Lead in Neuroscience youll be the driving force behind our Medical Safety organization championing innovative safety str...
Clinical Development Director
Rhygaze Ag
RhyGaze is an innovative growing biotech company developing next-generation therapies for serious eye diseases. We are seeking a highly motivated Clinical Development Director with expertise in ophthalmology particularly gene therapy to help advance our cutting-edge pipeline. Retina experience is re...
Device Documentation Lead
Ucb
Make your mark for patientsWe are looking for a Device Documentation Lead who is methodical detailfocused and qualitydriven to join our Devices Artwork & Packaging (DAP) team supporting the development and lifecycle of drugdevice combination products. This role can be based in BrainelAlleud Belgium...
Faas Senior Manager Regional Controller (ifms) Zur...
Ey Studio+ Nederland
At EY were all in to shape your future with confidence.Well help you succeed in a globally connected powerhouse of diverse teams and take your career wherever you want it to go.Join EY and help to build a better working world.EY is expanding its Integrated Finance Managed Services (IFMS) offering in...
(sr.) Site Activation Specialist (mwd), Office-bas...
Iqvia
IQVIA currently offers the exciting opportunity for a (Sr.) Site Activation Specialist (m/w/d) to work in the Country Site Activation Department in ourBasel office Switzerland.In this role you will perform tasks at a country level associated with clinical research site activation activities in accor...
Faas Manager Assistant Controller (ifms) Zurich, B...
Ey Studio+ Nederland
At EY were all in to shape your future with confidence.Well help you succeed in a globally connected powerhouse of diverse teams and take your career wherever you want it to go.Join EY and help to build a better working world.EY is expanding its Integrated Finance Managed Services (IFMS) offering in...
Director Biotherapeutics Rd
Johnson & Johnson
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...
Sr Scientist Biotherapeutics Rd
Johnson & Johnson
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...
Senior Director, Regulatory Affairs Cmc Europe & I...
Cytokinetics
Cytokineticsis a specialty cardiovascular biopharmaceutical company building on its over 25 years of pioneering scientific innovations in muscle biology and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction.Position SummaryThis is a pe...
Senior Director, Regulatory Affairs Cmc Europe
Cytokinetics
Cytokineticsis a specialty cardiovascular biopharmaceutical company building on its over 25 years of pioneering scientific innovations in muscle biology and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction.Reporting to the Executive D...
Director Associate Director – Toxicology
Monte Rosa Therapeutics
OverviewMonte Rosa Therapeutics is searching for a Toxicology Lead to direct nonclinical safety and toxicology work for programs to enable drug candidates from discovery through development. This position will lead and develop nonclinical toxicology strategies to support Monte Rosas diverse drug can...
Therapeutic Area Head, Pk Science- Neuroscience
Novartis
Job Description Summary#LI-Hybrid Internal Title: TA Head PKS NeuroscienceLocation: BaselWe are seeking an accomplished and visionary scientific leader to join us as TA Head PKS this highly visible role you will lead a cross-functional scientific organization spanning pharmacokinetics bioanalysis q...
Regulatory Affairs Expert
Tandem Diabetes Care International Sàrl
Job DescriptionGENERAL SUMMARY:The Regulatory Affairs Expert is responsible for developing and executing strategies to support products registrations entity set-up and ongoing compliance with country-specific requirements. Acting as the local subject matter expert the role ensures adherence to appli...
Senior Director, Epidemiologist
Novartis
Job Description SummaryThis is a seat at the table where science becomes strategy. As Senior Director Epidemiologist in the Quantitative Safety & Epidemiology Team you will define and drive global epidemiology direction across multiple oncology programs shaping benefit-risk decisions from developmen...
Scientist Stability (mfd) – Hybrid Role
Gloor&lang Ag
Stability testing Drug Substance/Product 7-Months contractExciting Opportunity in a Global Pharmaceutical EnvironmentFor our client a leading international biopharmaceutical company we are currently looking for a motivated and experienced Scientist Stability to join the Global Biopharmaceutical Stab...
Regulatory Affairs Postgraduate Program Switzerlan...
Novartis
Job Description SummaryThe Regulatory Affairs Postgraduate Training Program is an opportunity to discover the global functions of Regulatory Affairs and Regulatory Chemistry Manufacturing and Controls. Successful candidates will be offered a training position consisting of two rotational assignments...
Sr. Mgr, Regulatory Program Management
Johnson & Johnson
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...
Principal Scientist, Cmc Science
Csl Plasma
The Principle Scientist CMC Science is responsible for supporting and executing Chemistry Manufacturing and Controls (CMC) strategies for pharmaceutical and/or biologic products across clinical development and early commercialization. This role ensures that drug substance and drug product developmen...