REGULATORY AFFAIRS COPY REVIEW jobs in United Kingdom

Affairs team. Planning, coordination, and management of regulatory documentation activities. Review and compilation... and Medicine, Manufacturing, Scientific 12/04/2024 Omega Diagnostics Ltd are recruiting for a Regulatory Affairs Supervisor...

to translate novel technologies to the clinic. We welcome applications from individuals with experience in: Regulatory Affairs...We are seeking experts in medical device design regulatory processes to join our team and work with project groups...

technologies to the clinic. We welcome applications from individuals with experience in: Regulatory Affairs supporting MedTech.... About us We are seeking experts in medical device design regulatory processes to join our team and work with project groups to translate novel...

classes. Regulatory review and approval and advertising or promotional copy for Cosmetics and other non-OTC. Work with the... Regulatory Consultant Role: Regulatory review and approval of product labelling for Cosmetics and other non over the counter...

The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position... Regulatory Affairs - with experience in medicinal products. You will grow and maintain major portfolio in particular for the...

classes. Regulatory review and approval and advertising or promotional copy for Cosmetics and other non-OTC. Work with the... Regulatory Consultant Role: Regulatory review and approval of product labelling for Cosmetics and other non over the counter...

company portfolio in mainly UK & Ireland Regulatory review and approval and advertising or promotional copy for Cosmetics... Responsibilities and Deliverables: Regulatory review and approval of product labelling for Cosmetics and other non-OTC classes per the...

and regulatory bodies. The post holder will also work with relevant professional team to ensure scanning protocols and SOPs are in... to submit a copy of their CV, and a supporting statement, detailing how they meet the essential criteria listed in the advert...

, contributing to the authorship and review of regulatory documents, leading multi-jurisdiction programs, and representing clients in... area of biotechnology and regulatory affairs Clinical development experience across a range of therapeutic indications...

affairs. This role will involve providing strategic, technical, and regulatory advice to clients in the development of human... authorship and review of regulatory documents and provide leadership within the consultancy team. Please note...

affairs. This role will involve providing strategic, technical, and regulatory advice to clients in the development of human... authorship and review of regulatory documents and provide leadership within the consultancy team. Please note...

relations activities; collaborative initiatives etc.. · Labelling support: Input to and review of regulatory applications... to join Norgine. The person holding this position will report to Senior Global Director of Medical Affairs and be a member of the...

relations activities; collaborative initiatives etc.. · Labelling support: Input to and review of regulatory applications... to join Norgine. The person holding this position will report to Senior Global Director of Medical Affairs and be a member of the...

with Product Category Managers, R&D and Regulatory Affairs for technical claims communication audit/s and maintain copy compliance... campaign copy Support Global PR team with review of press materials Lead key process improvement initiatives for Product...

with Product Category Managers, R&D and Regulatory Affairs for technical claims communication audit/s and maintain copy compliance... campaign copy Support Global PR team with review of press materials Lead key process improvement initiatives for Product...

on Discovery & Translational Science, Bioinformatics, and Regulatory Affairs & Intelligence 3.) Technology Consulting... this role? Undertake systematic literature review projects (protocol, screening, data extraction, quality control, qualitative...

assets or in clinical development and/or the post-marketing setting. Our safety group ensures scientifically sound review... and interpretation of data and management of safety issues and escalates safety issues identified through the safety review process...