regulatory affairs associate

Teleflex is seeking an Associate Regulatory Affairs Specialist (3-year contract) to ensure medical devices are developed, manufactured and registered in Europe, US and Canada.The role coordinates regulatory changes, maintains documentation, and supports CE/US/Japan registrations. Fluency in English is mandatory; university degree in a relevant field...

Teleflex in Zürich, Switzerland seeks a Regulatory professional to ensure vascular intervention medical devices are developed, manufactured and registered in line with global healthcare laws. You will manage regulatory assessments of changes and maintain worldwide documentation.Responsibilities include design/manufacturing change assessment, supporting...

pAcadia Pharmaceuticals is seeking an Associate Director of Regulatory Affairs Europe to lead regulatory development, submission and lifecycle maintenance for products in Europe. The role requires experience in EU regulatory strategy, cross-functional collaboration, and managing major submission components. /ppThe successful candidate will drive regulatory...

Acadia Pharmaceuticals is seeking an Associate Director of Regulatory Affairs Europe to lead regulatory development, submission and lifecycle maintenance for products in Europe. The role requires experience in EU regulatory strategy, cross-functional collaboration, and managing major submission components.The successful candidate will drive regulatory...

Primary purpose of the position: The Associate Director, Regulatory Affairs leads IFPMA's policy and regulatory strategies on manufacturing innovation, quality systems, good manufacturing practices and reliance while ensuring cross-team integration. In addition, provides technical and functional leadership for strategically relevant regulatory policy areas....

About Acadia PharmaceuticalsAcadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson’s disease psychosis and Rett syndrome. We are developing the...

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...

ph3Position Summary /h3 pThe Associate Director, Regulatory Affairs Europe is responsible for the implementation and execution of global regulatory development, submission and lifecycle maintenance strategies for assigned products in Europe. Staying abreast of the ever evolving regulatory and therapeutic landscapes, the Associate Director will inform...

h3About Acadia Pharmaceuticals /h3pAcadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson’s disease psychosis and Rett syndrome. We are...

About Acadia PharmaceuticalsAcadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson’s disease psychosis and Rett syndrome. We are developing the...

ppbAbout Acadia Pharmaceuticals /bAcadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson’s disease psychosis and Rett syndrome. We are...

Select how often (in days) to receive an alert:As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine,...

h3bCareer Category /b /h3pRegulatory /ph3bJob Description /b /h3pIf you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching,...

pIf you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that read over...

h3Career Category Regulatory Job Description /h3pIf you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and...

Regulatory Job Description If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better...

If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that read over 10...

ph3Overview /h3pMonte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of CMC Regulatory Affairs. The CMC Regulatory Affairs will serve as a key regulatory strategist and author for the Chemistry, Manufacturing, and Controls components of Monte Rosa's global regulatory filings....

ph3Overview /h3pMonte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of CMC Regulatory Affairs. The CMC Regulatory Affairs will serve as a key regulatory strategist and author for the Chemistry, Manufacturing, and Controls components of Monte Rosa's global regulatory filings....

Monte Rosa Therapeutics, Inc is seeking an Associate Director of CMC Regulatory Affairs to lead global regulatory strategies for Chemistry, Manufacturing, and Controls across development stages. You will author Module 3 content, review summaries, and partner with Process Chemistry, Analytical Development, Drug Product, Quality, and Clinical Supply teams to...