Regulatory jobs

• United States of America
• Negotiable
• Posted 2 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...

• Nottingham
• Negotiable
• Posted 2 days ago

We have a current opportunity for a Regulatory / Medical Writer on a contract basis for up to 40 hours per week. The position will be fully remote, dedicated to a renowned CRO. Experience within oncology is desired. Further information about this position please apply.

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

A leading organization in the pharmaceutical and regulatory affairs industry, dedicated to increasing project efficiency and establishing project management standards; are looking for a talented and experienced Project Manager to join the Project Management Office (PMO) team. Key Responsibilities...

• Cork
• Negotiable
• Posted 15 days ago

Role: Clinical Evaluation Specialist Consultant Tasks: Writing Clinical Evaluation Plans Writing Clinical Evaluation Reports Post market Clinical Follow Up Plans & Reports All focusing around EU Medical Device Regulation with a specific focus on Implantable Bio-materials. Start date: ASAP Contrac...

• Barcelona
• Negotiable
• Posted 17 days ago

I am working with a highly innovative biotech company based in Barcelona, specializing in the development of groundbreaking medical devices. We are looking for a Regulatory Affairs & Quality Assurance Specialist to join their team. Ideal Profile: Experience in regulatory strategies and documentat...

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

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