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• United States of America
• Negotiable
• Posted 4 days ago

Job Overview The Clinical Evaluation Reporting Specialist is tasked with creating Clinical Evaluation Reports (CERs) for Terumo Blood and Cell Technologies (TBCT) products. This involves utilizing product labeling, preclinical and clinical data, published literature, risk management documents, co...

• Italy
• Negotiable
• Posted 5 days ago

ABOUT US We are a European organization recognized as an official Notified Body under Regulation (EU) 2017/745, specializing in verifying the conformity of medical devices with the stringent requirements of the MDR 2017/745 regulation. Our work ensures that medical devices meet the necessary stan...

• Connecticut
• US$160000 - US$200000 per annum
• Posted 7 days ago

Title: Director Regulatory Affairs A small sized diagnostics company is seeking a Director of Regulatory Affairs to lead the regulatory submissions, strategy, and maintenance activities for their existing products and new products in development. They are pioneering the field with innovative mach...

• Philadelphia
• Up to US$225000 per annum
• Posted 7 days ago

Director of Regulatory Affairs Strategy This position is with a rapidly growing pharmaceutical company known for its commitment to advancing transformative therapies. In this role you will have a unique opportunity to lead regulatory strategies for innovative pharmaceutical products, making a mea...

• Connecticut
• US$160000 - US$200000 per annum
• Posted 26 days ago

Title: Director Regulatory Affairs A small sized diagnostics company is seeking a Director of Regulatory Affairs to lead the regulatory submissions, strategy, and maintenance activities for their existing products and new products in development. They are pioneering the field with innovative mach...