Trabajo Regulatory Affairs

We invite you to bring your knowledge of European regulations governing product safety and stewardship into play as you support organisations around the world bring to the market products in a range of uses that meet relevant requirements and are safe for human health and the environment. The ideal ...

¿Tienes experiencia como en gestión de la documentación como Regulatory Affairs? ¿Te gustaría trabajar en una de las principales empresas del sector químico de la zona del Alt Penedés? Si es así... sigue leyendo, ¡esta oferta te interesa!Empresa química principal fabricante en Europa de productos qu...

Business Development Lead Global Health Job Purpose This role is critical to support senior management as well as Gov Affairs and Global functions by providing expert BD support and leadership on a range of activities covering the strategic design of Global Health (GH) partnerships based on the need...

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...

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...

**Company Description**We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within:...

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....

As a leading contract development and manufacturing organization (CDMO) within the pharmaceutical industry, Ardena is dedicated to supporting pharmaceutical companies, from virtual biotech to major players, in bringing their valuable molecules to the clinic and market. Our commitment extends to prov...

Post Market Quality, Regulatory and Vigilance Senior Specialist page is loaded Post Market Quality, Regulatory and Vigilance Senior Specialist Apply locations ESP - Malaga time type Full time posted on Posted Yesterday job requisition id JR104765 Do you want a job with a purpose?And do you want to m...

Medical Information Associate- Italian languageFull-timeDepartment: Medical InformationWe are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially established in 2008. We are proud to have achieved global organic growth year after year, with staff...

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...

Auditor & Product Expert for IVD Expert Devices- As a Product Specialist/Expert you evaluate IVD Expert medical products in accordance with European guidelines and standards. You are responsible for the review of the technical documentation of selected product groups in non-active products area in y...

DescriptionPrincipal Medical WriterSyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Developmen...