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Regulatory Affairs Jobs in Basel

1 - 15 of 27
1 - 15 of 27
Search Results - Regulatory Affairs Jobs in Basel
EPM Scientific-Basel
Regulatory Affairs & CMC Ready to make a real impact in regulatory affairs? We're looking for a dynamic Regulatory Affairs Expert (CMC & Compliance) to join a leading international pharmaceutical manufacturer. In this role, you'll help define global...
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Uniboard-Basel
<< ZURÜCK BEWERBEN von: Uniboard Student Internship in Technical Regulatory Affairs (starting September 2025, 12 Months, in Basel) Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing...
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stellen-basel.ch -
Novartis Farmacéutica-Basel
Regulatory Affairs team.The role involves directing the development and submission of regulatory documents, providing strategic direction and negotiating with agencies to expedite approvals. It also ensures timely approval and compliance of new and marketed...
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appcast.io -
Novartis-Basel
is responsible is an advantage.  •  Demonstrable experience in Pharmaceutical Industry within Medical Affairs and/or Clinical Development. Firm working knowledge of GCP, scientific and clinical methodology, protocol designs, management and regulatory requirements...
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Novartis Farmacéutica-Basel
into analysis and interpretation of scientific data, to key documentation, - Leverage scientific knowledge and acumen in the analysis, interpretation and communication of data to colleagues. Lead interactions with Regulatory Affairs and Development Unit...
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appcast.io -
Boehringer Ingelheim-Basel
and/or regulatory affairs Proven experience as a medical advisor or Medical Science Liaison in prescription medicines Strong clinical and/or scientific experience in at least one of our active therapeutic areas: cardiovascular, renal, metabolic Experience...
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Novartis Farmacéutica-Basel
Job Description Summary As a member of the Knowledge & Content Management Platform team, the Knowledge Management Capability Lead contributes to the strategic vision of Regulatory Affairs and supports the digitalization and centralization...
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Syneos Health Commercial Solutions-Basel
As Oncology Field Medical Affairs, your day may include: Building and maintaining relationships with key therapeutic area experts and investigators to foster collaboration and insights. Responding to inquiries about study indications, disease states...
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F. Hoffmann-La Roche AG-Basel
related to the medical affairs activities within the designated disease area(s).  •  Ensure alignment with regulatory and ethical standards, collaborating with relevant departments to maintain high-quality standards.  •  Drive, embed and maintain a culture...
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Roche-Basel
of collaboration with a very close liaison between early and late-stage functions You have a demonstrated experience of Phase II - III drug development You will take an active role with other CST members, regulatory and other internal partners/stakeholders...
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Coopers Group GmbH-Basel
Duration: 1 year Readytotravelinternationally-Europe,US,APAC-10-20% The CTSM serves as a broker role between study vendors involved in IMP packaging and further management (e.g. Packaging and Labelling CMO), Clinical development, Regulatory...
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Sobi-Basel
e.g. Operations, Regulatory Affairs, Supply Chain, Validation, IT) to implement and sustain GMP requirements within the quality systems.  •  Work closely with global QA and IT teams to maintain and enhance electronic Quality Management Systems (eQMS...
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stellen-basel.ch -
Roche-Basel
satisfaction and maximize business value for patients, the healthcare system and Roche. You will work in a dynamic environment and collaborate across the RPS network (Marketing, Medical, Pipeline, Supply Chain, Regulatory Affairs, Patient Partnership, Quality...
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roche.com -
ARX | smart minds-Basel
Elektroinstallationen Gebäudetechnik Vice President / Bereichsleiter Qualitymanagement & Regulatory Affairs (m/w/d) Rheinfelden (Baden), Baden-Württemberg, Germany 3 weeks ago Oftringen, Aargau, Switzerland 2 weeks ago #J-18808-Ljbffr...
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Novartis-Basel
is an advantage. Demonstrable experience in Pharmaceutical Industry within Medical Affairs and/or Clinical Development. Firm working knowledge of GCP, scientific and clinical methodology, protocol designs, management and regulatory requirements for clinical...
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