Trabajo Regulatory Affairs Manager

Pharmacovigilance Quality Assurance Lead page is loaded Pharmacovigilance Quality Assurance Lead Apply locations Barcelona time type Full time posted on Posted 4 Days Ago job requisition id JR008704 With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the pu...

Do you have a solid knowledge of European regulations regarding product safety and stewardship? Are you eager to use your expertise to support global organizations in bringing safe, health and environment friendly products to the market? Does the idea of collaborating with an international team and ...

Vantive: A New Company Built On Our LegacyBaxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Va...

Yes, you, individuals eager to start new professional adventures.Who we are?QGMI is a global infrastructure group specialised in the development, structuring and implementation of infrastructure projects.Within our company, we're dedicated to exceeding the expectations of our clients, navigating the...

Pharmacovigilance Quality Assurance Lead With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and s...

Global Project Manager, Regulatory AffairsDo you love playing an integral role in driving innovation in a new and transformational industry? Are you passionate about the environment? Do you want to play a part in supporting the world’s farmers to adopt new methods of sustainable agriculture?Suterra ...

With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that spans the full spectrum of t...

Manage day-to-day operations of the Cargolux (CV) Compliance ProgramDesign, implement & monitor effective measures aiming to manage adequately Compliance related risks in Cargolux linked to the topics of Anti-Corruption, Anti-Trust, Fraud and AML, GDPR. Additionally, some involvement in Export Contr...

Precision for Medicine (CRO) are recruiting a Regulatory Manager to join our team, candidates can be based in the following countries: UK, Spain, Hungary, Slovakia, Serbia, Romania or Poland. Position Summary: The Regulatory Manager (RM) provides regulatory strategy and development guidance for opti...

This position it's intended for a person with broad skills in the most used and well known biotechnology and cellular biology techniques, as well as knowledge of the market trends and the latest technology updates. Whithin the Life Science department, the individual will contribute in the implementa...

Winid is a talent acquisition consultancy that offers Executive Search, RPO and Talent Solutions. Our purpose is to drive the growth and fulfillment of individuals and organizations. We facilitate individuals in finding inspiring opportunities and help organizations discover professionals who will t...

1 week ago Be among the first 25 applicants Direct message the job poster from RED GlobalQuality and Compliance Lead - Contract - 6 months - RemoteAs Quality and Compliance Lead you will play a pivotal role within the Digital team, offering vital expertise in Quality and Compliance. A core focus inv...

Regional Regulatory Director page is loaded Regional Regulatory Director Apply locations Remote - Spain time type Full time posted on Posted 6 Days Ago job requisition id R-1516 Vantage is a leading supplier of naturally derived specialty ingredients and formulations that cater to the evolving needs...

Employment Type: Permanent Contract Duration: At IATA, we speak for the airlines of the world, serving and supporting over 300 of them across all continents. We are passionate and knowledgeable about the aviation industry, and we strive to make it safer, smarter, more sustainable and more inclusive....

Join Caidya as a Senior Study Start-Up Lead (Sr. SSUL). You'll focus on managing the submission of global applications for clinical trials. The ideal candidate will independently handle CORE study documents, understand regulatory submissions globally, and manage submission processes with ethics comm...