Regulatory Specialist jobs

• United States of America
• Negotiable
• Posted 7 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 8 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 8 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 1 month 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 1 month 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 1 month 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...

• 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...

• Germany
• Negotiable
• Posted about 2 months ago

Job Title: Labelling Specialist - Exciting Freelance Opportunity in Medical Device Sector Location: Germany (Remote/On-site) Leading medical device company committed to improving patient outcomes through innovative solutions. their products, including Class II medical devices, are used globally, ...

• Florida
• Negotiable
• Posted about 2 months ago

Here is your chance to join an innovative and cutting-edge medical device company! The company I am supporting has innovated and launched over 100 products and doesn't plan on slowing down any time soon. This company dominates the market share, and its products can be found in over 50 countries. ...

• United States of America
• Negotiable
• Posted about 2 months ago

Here is your chance to join an innovative and cutting-edge medical device company! The company I am supporting has innovated and launched over 100 products and doesn't plan on slowing down any time soon. This company dominates the market share, and its products can be found in over 50 countries. ...