All jobs near North America

• Massachusetts
• Negotiable
• Posted 14 days ago

We have a current opportunity for a Regulatory Affairs Specialist on a contract basis. The Regulatory Affairs Consultant will be responsible for providing strategic guidance on regulatory requirements and submissions for medical devices. This role involves ensuring compliance with global regulati...

• New Jersey
• US$75000 - US$90000 per annum
• Posted about 1 month ago

Title: Senior Associate of Regulatory Affairs Summary: A leading, global pharmaceutical client of ours is looking to hire a Senior Associate of Regulatory Affairs, based out of their New Jersey office. This rapidly growing client has drug products spanning generics, branded prescriptions, and inj...

• New Jersey
• Negotiable
• Posted about 1 month ago

Title: Senior Associate of Regulatory Operations/CMC Summary: A leading, global pharmaceutical client of ours is looking to hire a Senior Associate of Regulatory Operations and CMC, based out of their New Jersey office. This rapidly growing client has drug products spanning generics, branded pres...

• Morristown
• Negotiable
• Posted about 1 month ago

Job Title: Senior Associate, Regulatory Affairs Location: Morristown, New Jersey About the Role: We are seeking a highly motivated and detail-oriented Senior Associate, Regulatory Affairs to join our team. In this role, you will help author, compile, review, and submit high-quality regulatory sub...

• United States of America
• Negotiable
• Posted about 1 month ago

* Authoring high-quality CMC documentation for US/ EU / UK countries, with support and guidance, applying agreed CMC global regulatory strategies, assuring technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements throughout project lifecycle. * P...

• Cincinnati
• US$90000 - US$120000 per annum
• Posted about 2 months ago

Title: Senior Regulatory Affairs and Quality Systems Specialist The Regulatory Affairs and Quality Systems Specialist is responsible for supporting regulatory and quality assurance processes related to in vitro diagnostic (IVD) medical devices. This organization offers a dynamic and collaborative...