Regulatory Affairs – Senior CMC Dossier Manager

Reference Number: JO Associate Director, Regulatory Affairs CMC Rate: Negotiable Job Type: Permanent Location: Hatfield Associate Director, Regulatory Affairs CMC/ Senior Manager Hertfordshire, UK An exciting opportunity to join an established pharmaceutical company that specialises in Oncology and Neurology. The role will be working across both...

Senior Manager Regulatory Affairs CMC | Biologics | RemoteSenior Regulatory Affairs Manager CMC Role available for an innovative, world renowned, research-based biopharmaceutical company that focuses on the discovery, development, and commercialisation of new, cutting edge medicines. Specialising in therapeutic areassuch as Viral Diseases, Inflammatory...

BioTalent are pleased to be supporting a longstanding client, a mid-sized biopharmaceutical business with offices across Europe, in their search for a Senior Manager Regulatory CMC, responsible for Dossier Management.The client would like to speak to candidates with experience in:Developmentactivities forBiologicsin theEUandUS.nPost-approvalactivities...

BioTalent are pleased to be supporting a longstanding client, a mid-sized biopharmaceutical business with offices across Europe, in their search for a Senior Manager Regulatory CMC, responsible for Dossier Management.The client would like to speak to candidates with experience in:Developmentactivities forBiologicsin theEUandUS.nPost-approvalactivities...

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Associate Director, Regulatory Affairs CMC Associate Director, Regulatory Affairs CMC United Kingdom - Uxbridge, United Kingdom - Cambridge Regulatory Regular Job Description At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly...

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...

We are an industry-leading independent scientific consultancy providing Pharmaceutical and Biotechnology clients throughout the world with expert Regulatory Affairs consultancy and Quality Assurance solutions.As demand for our services and solutions continues to grow we are looking for a CMC consultant to join our team of Regulatory Affairs professionals on...

An exceptional opportunity awaits with our client, a dynamic Regulatory Affairs Consultancy with a presence in the UK, Switzerland, and Ireland, serving global clients. In this role, you will join a team of seasoned experts in Regulatory, CMC, Clinical, and Non-Clinical fields, leveraging your CMC and Regulatory expertise to provide comprehensive support and...

An exceptional opportunity awaits with our client, a dynamic Regulatory Affairs Consultancy with a presence in the UK, Switzerland, and Ireland, serving global clients. In this role, you will join a team of seasoned experts in Regulatory, CMC, Clinical, and Non-Clinical fields, leveraging your CMC and Regulatory expertise to provide comprehensive support and...

Are you looking for a new opportunity where your expertise will be pivotal in navigating the complexities of UK/EU regulatory frameworks? Based in Berkshire, this role offers the chance to become an integral part of a leading Pharmaceutical company, ensuring that innovative health solutions reach the market efficiently and safely. As a Regulatory Affairs...

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...

Job Description Regulatory CMC Consultant Join an unprecedented team, supporting a range of different projects. In this role, you will be driving a number of projects, including developing the eCTD for BLA filngs of Biologicals. Responsibilities: Represents the department on multi-functional project development teams to support regulatory filings ...

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...

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...

Job Title:Regulatory Affairs Specialist - Medical DeviceLocation:Fully remoteCompany Description:We are a leading healthcare company dedicated to improving patient outcomes through innovative medical technologies.nOur commitment to quality and compliance drives us to seek talented professionals to join our Regulatory Affairs team.Position Overview:As a...

Regulatory Affairs Specialist - Medical Device 3 weeks ago Be among the first 25 applicants Job Title: Regulatory Affairs Specialist - Medical Device Location: Fully remote Company Description: We are a leading healthcare company dedicated to improving patient outcomes through innovative medical technologies. Our commitment to quality and compliance...

Job Description Our client, an independent pharmaceutical company who manufacture and specialising in generics, have an opportunity for an experienced EU/ UK Regulatory team leader to join their team in Hampshire. As Regulatory Affairs manager, you will: Leading a small team, handling the regulatory activity across a large portfolio of medicine and...

Proclinical is seeking a Director for Global Regulatory Affairs CMC. The successful candidate will be responsible for authoring global quality regulatory documentation for multiple medium-complexity projects. The role also involves defining and establishing platform approaches to the preparation of quality regulatory documentation used in development,...

Job Title:Senior Regulatory Affairs OfficernEmployment Type:PermanentnLocation:East London, 3 days on-site per week.(Hybrid)nSalary:Up to £50,000Senior Regulatory Affairs Officer opportunity working for a growing pharmaceutical company that specialising in medicinal, non-medicinal, medical devices, and OTC products. The business is increasingly growing and...