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Act as a subject matter expert on global regulatory requirements, including for ATMPs, ensuring company-wide compliance and integrating relevant regulatory intelligence. Lead regulatory interactions with authorities such as the FDA, EMA, and national agencies, while overseeing the preparation and...

Job Title: Lead Factory Trainer (Maternity Cover- 12 months)Department: Group People and DevelopmentReports To: Factory Training ManagerLocation: Site BasedShift Pattern: Monday to Friday 12:00pm to 09:00pm (Tuesday and Wednesday) 8:00am to 5:00pm (Monday, Thursday and Friday)Pay Rate: Competitiv...

Regulatory Affairs Manager / Regional Regulatory Lead. Regulatory Strategy Development: Lead the development of regulatory strategies for CTAs in alignment with EU regulatory requirements. To act as the subject matter expert (SME) and provide valid regulatory guidance to support ongoing regulator...

Senior Manager, Regulatory Medical Writing. May act as the departmental expert on IND/IMPD dossier components, briefing documents, and responses to regulatory authorities across programs. Reviews documents within a therapeutic area with respect to consistency with the team/corporate established s...

Are you a hands-on Regulatory Affairs professional with a passion for clinical trials and a drive to grow into leadership? Join a dynamic, fast-paced SME-sized CRO specialising in oncology, where your expertise will shape the future of our expanding Regulatory Affairs team. Senior Clinical Regula...

We are working exclusively with a well-established and growing UK-based manufacturer of bespoke cleaning and hygiene chemical products is seeking a talented Development & Regulatory Chemist Manager. The company operates under internationally recognised quality standards and is committed to contin...

Mantell Associates is currently partnered with an exciting Biomedical Research organisation, who are looking to bring in a Global Regulatory Affairs Senior Manager to take the company to new heights as they continue to grow. Senior Manager Global Regulatory Affairs - Requirements:. Demonstrated s...

Senior Manager, Regulatory Medical Writing. Demonstrated and substantial experience in leading/managing the creation of IND/IMPD and NDA/MAA components, briefing documents, and responses to regulatory authorities. The individual provides leadership with respect to all program documents and may ac...

Regulatory Strategy Development: Lead the development of regulatory strategies for CTAs in alignment with EU regulatory requirements. Regulatory Affairs Manager / Regional Regulatory Lead. Regulatory Intelligence: Stay current on regional regulatory changes, guidelines, and best practices related...