Regulatory Specialist jobs

• Northern Ireland
• Negotiable
• Posted 3 days ago

We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis. Please apply if you have the skill set and are interested: 6-12 months project Full time (39 hours per week) Hybrid Start - May/June IVDR Regulatory Knowledge, getting ready for clinical trials. GAP Asse...

• Northern Ireland
• Negotiable
• Posted 3 days ago

We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis in Northern Ireland. Please apply if you have the skill set and are interested: 6-12 months project Full time (39 hours per week) Hybrid Start - May/June IVDR Regulatory Knowledge, getting ready for clini...

• Kuala Lumpur
• Negotiable
• Posted 5 days ago

Job Title: Regulatory Affairs Quality Assurance (RAQA) Executive Location: Kuala Lumpur, Malaysia About Us: Our client is a leading medical device company dedicated to improving healthcare through innovative medical devices. Our commitment to quality and regulatory compliance ensures that our pro...

• Malaysia
• Negotiable
• Posted 7 days ago

Job Title: Regulatory Affairs Quality Assurance Executive Location: Malaysia About Us: Our client is a leading medical device company dedicated to improving healthcare through innovative medical devices. Their commitment to quality and regulatory compliance ensures that our products meet the high...

• Negotiable
• Posted 7 days ago

Job Title: Regulatory Affairs Quality Assurance Executive Location: Malaysia About Us: Our client is a leading medical device company dedicated to improving healthcare through innovative medical devices. Their commitment to quality and regulatory compliance ensures that our products meet the high...

• New Jersey
• US$75000 - US$90000 per annum
• Posted 10 days 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 10 days 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 11 days 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 17 days 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...

• Tokyo
• Negotiable
• Posted 28 days ago

Job Title: Regulatory Affairs Specialist Location: Tokyo, Japan Job Type: Full-time (permanent) Our client, a leading pharmaceutical company dedicated to improving global health through innovative medicines. They are committed to excellence in research, development, and regulatory compliance. Job...

• 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...

• Atlanta
• Negotiable
• Posted about 2 months 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 about 2 months 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 about 2 months 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 about 2 months 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...