Global Regulatory Submission Manager

Our Development Team is guided by our purpose: to reimagine medicineto improve and extend people's lives.To do this, we are optimizing and strengthening our processes and ways of working. We are investing in new technologies and building specific therapeutic area and platform depth and capabilities – all to bring our medicines to patientseven faster.We...

Role - Principal Regulatory Affairs Specialist Location - Hampshire or Remote ( must be based in UK or Europe ) Salary - Negotiable Role Status- Perm Scope: Supports Regulatory Affairs Project core team members on development teams, providing regulatory guidance, and project regulatory assessments. Liaises with internal functions such as Manufacturing,...

We Want You for Our Team! This global manufacturer is in search of an exceptional regulatory specialist with at least 5 years of experience in the regulatory field. If you are up for a challenge and ready to showcase your skills, this position might be the perfect fit! About the Company: Looking for a Senior Regulatory Affairs Specialist Focus on MENA...

Regulatory Affairs Manager, Global Regulatory Affairs Pharmaceuticals, EU page is loaded Regulatory Affairs Manager, Global Regulatory Affairs Pharmaceuticals, EU Apply locations UK - Hook IT - Milano AT - Vienna BE - Antwerp ES - Madrid time type Full time posted on Posted 2 Days Ago job requisition id R At Elanco (NYSE: ELAN) – it all starts with...

Global Regulatory Compliance Manager – London – £50-60, Do you have an eye for detail and accuracy, even in a fast-paced environment? Are you ready to create compliant products that captivate consumers? Join one of the world's fastest-growing and most influential beauty brands and take responsibility for regulatory compliance and all related...

Our Client is a leading biopharmaceutical company dedicated to discovering, developing, and delivering innovative therapies that improve the lives of patients. Their commitment to excellence is reflected in our pioneering research, groundbreaking treatments, and unwavering dedication to quality and compliance for innovative medicines. Position Summary:The...

Precision for Medicine (CRO) are recruiting a Regulatory Manager to join our team, candidates can be based in the following countries: UK, Spain, Hungary, Slovakia, Serbia, Romania or Poland. The Regulatory Manager (RM) provides regulatory strategy and development guidance for optimal conduct of clinical trials, regulatory agency meetings, orphan...

An opportunity to join the Product Stewardship / Regulatory Compliance team at a global chemical business; you will ensure the compliance of globally sold, highly complex mixtures.Key duties will be SDS authoring, classifications, labelling, component compliance checks and providing regulatory advice to the technology, R&D, and customer service teams.This is...

Position:Regulatory Affairs ManagernLocation:Uxbridge (UK)nContract Length:6-month (View to extend)nWork Structure:Monday - FridaynPay Rate:Available on request - (Inside IR35)The new Regulatory Affairs Manager must be an individual who has proven experience within a CMC (Chemistry, Manufacturing & Controls) focused environment.The client is a leading global...

Our Development Team is guided by our purpose: to reimagine medicineto improve and extend people's lives.We are investing in new technologies and building specific therapeutic area and platform depth and capabilities – all to bring our medicines to patientseven faster.We are seeking key talent, like you, to join us and help give people with disease and...

Position: Regulatory Affairs ManagerLocation: Uxbridge (UK)Contract Length: 6-month (View to extend)Work Structure: Monday - FridayPay Rate: Available on request - (Inside IR35)The new Regulatory Affairs Manager must be an individual who has proven experience within a CMC (Chemistry, Manufacturing & Controls) focused environment.The client is a leading...

Regulatory Affairs Manager- (EU CTR) Homebased in UK/Ireland OnlyDue to recent success within one our Innovative Biotech Clients I am recruiting for a Regulatory Affairs manager at ICON - Working in a client-dedicated yet fully embedded role ICON's Regulatory Strategy group, you will lead or contribute to the development and execution of the drug development...

Regulatory Publishing Associate or Specialist Job ID REQ Our Regulatory Operations Team is guided by our purpose: to reimagine medicineto improve and extend people's lives.We are investing in new technologies and building specific therapeutic area and platform depth and capabilities – all to bring our medicines to patients even faster.We are seeking key...

Senior Global Program Regulatory Manager Job ID REQ Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people's lives.We are investing in new technologies and building specific therapeutic area and platform depth and capabilities – all to bring our medicines to patientseven faster.We are seeking key talent, like...

Why Join Us? Be a hero for our rare disease patients_Our commitment and care for patients extends to our people, so culture is an essential cornerstone for Ultragenyx. We remain continuously focused on creating a supportive and inclusive environment of profound learning and growth - so employees can thrive in all areas of their lives, in and outside of work....

Regulatory Affairs Manager CMCDuration: 6 month Contract Inside IR35Location: Uxbridge, 3 days on-site per weekHourly Rate: £40-£55 per hour dependent on experience.This role focuses on the critical aspect of Chemistry, Manufacturing, and Controls (CMC) within regulatory affairs.Responsibilities include:Leading global regulatory strategies with a strong...

Location: London, UK (or Boston, US)Reporting to: Director, Regulatory Science Early-Stage Programs Job SummaryThis role will report to the Director, Regulatory Science for Early-Stage programs. The successful candidate will have the opportunity to primarily work with Global and Regional Regulatory Leads who are responsible to develop the regulatory strategy...

Device Regulatory Affairs, Senior Director This is a rare opportunity to join a young, exciting clinical-stage biotechnology company. Our client is focused on the discovery and development of novel therapies, with the potential to fundamentally change the course of progressive, debilitating diseases. With an impressive proven track record of success in...

Closing Date: Thursday 30 May at 5pm GMT.REPORTING RELATIONSHIP: Director Global Project OperationsTEAM/PROGRAM: Academic Project OperationsFULL TIME EQUIVALENT: 1 FTECAREER STEP: Specialist (Projects)EMPLOYMENT DURATION: Per contract (2-3 years)START DATE: ASAPAbout The George Institute for Global HealthThe George Institute for Global Health was established...

The role forms part of Citi ICG Operations leadership team and is responsible for the management and oversight of all the ICG Operations functions supporting Global Markets as well as the Regulatory (Reg) reporting team, performing trade and transaction reporting.This role is being created as a result of consolidating two existing functions to ensure more...