Regulatory Specialist jobs

• Cincinnati
• US$90000 - US$120000 per annum
• Posted 5 days 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...

• Atlanta
• Negotiable
• Posted 14 days ago

Quality Specialist - Regulatory Affairs Overview: Join an industry leading biotech organization leading development of In vitro Diagnostic Medical Devices. This expert role within the Quality Assurance team involves supporting regulatory activities for In vitro Diagnostic Medical Devices. You wil...

• United States of America
• Negotiable
• Posted 21 days ago

Regulatory Affairs Contractor (Remote, USA) As a Regulatory Affairs Contractor, you will support the development and implementation of global regulatory CMC strategies for our partners' marketed and development products. You will assist with regulatory activities for both internal and external pr...

• Singapore
• Negotiable
• Posted 22 days ago

Job Title: Regulatory Pharmacist Location: Singapore About Us: Our client is a leading innovator in the pharmaceutical industry, dedicated to advancing healthcare through cutting-edge research and development. Our client specializes in developing groundbreaking therapies and medications that addr...

• Seoul
• Negotiable
• Posted 22 days ago

Job Title: Quality and Regulatory Specialist Location: Seoul, South Korea About the Company: Our client is a leading innovator in the biotech industry, dedicated to advancing healthcare through cutting-edge research and development. Our client specializes in developing groundbreaking therapies an...

• 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...

• 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...

• Denmark
• Negotiable
• Posted about 2 months ago

EPM Scientific are looking for a team of experienced consultants, to join our Medical Device client based near Copenhagen, Denmark. The initial project is focussed around a 510k submission, once completed focus will shift towards improving and maintaing compliance to ISO 13485. We are looking for...