Senior Scientific and Regulatory Affairs

An opportunity to join the Regulatory Affairs team at an R&D focussed global PPP company. You will:Manage a portfolio of plant protection products in specific geographical territoriesDevelop regulatory strategy Become the subject matter expert on the regulations/guidelines in your territory. As a regulatory Specialist, you will develop regulatory strategy...

Exciting opportunity to join the regulatory affairs team at an established and highly reputable chemical regulatory science consultancy. This is expansion to cover an increasing workload. The role is delivery focussed with no commercial or business development aspects. We are looking for a regulatory person for a purely regulatory delivery role. This role...

An excellent opportunity to join an ambitious UK based chemical regulatory compliance consultancy. Working closely with the highly experienced and respected Principal Consultant, you will undertake a range of regulatory activities including:Study monitoringWriting up study reportsRisk assessmentsDossier preparationDeveloping regulatory strategyConsortia...

Cure Talent are delighted to be working with a well-established Medical Device company that supply and distribute innovative Medical Devices. Due to their continued growth and success, we have an exciting opportunity for a Senior Regulatory Affairs Associate to join them in West Yorkshire.As the new Senior Regulatory Affairs Associate, you will be working...

A global pharmaceutical company based in Uxbridge is currently looking for a Senior Regulatory Affairs Manager to join their team.You will be a confident Regulatory Lead looking to work in an innovative therapy area, developing and defining regulatory plans across multiple products.This is a great opportunity to work with a team who take provide in working...

Medical Affairs Senior Advisor/Manager - 06 months contract - £43.68 p/h to £58.24 p/h (Depending upon experience)Job Description: Medical Affairs (Senior) Advisor/Manager If you are innovative and passionate about healthcare and want a role where you can drive change and make a difference, this could be one for you.In the Specialty Care Business Unit, we...

Brilliant entry level opportunty for graduates with a scientific background. You will join the team as Raw Material Specialist working with both the R&D team and Suppliers. The function of the role is to support the technical aspects of managing raw material data, building awareness of key chemical legislations (REACH, CLP, GPSR, CSR). You will recieve...

We are looking for a Senior Regulatory Affairs Manager/Consultant with 10+ years of experience in regulatory affairs, including CMC expertise. This challenging role offers the opportunity to work on diverse projects, manage client relationships, and contribute to regulatory strategies in a global pharmaceutical environment.This is a client dedicated project,...

Cure Talent is delighted to be partnered with a global Medical Device company, specialising in emergency medical products, who due to their exceptional continued growth, have an exciting opportunity for Regulatory Affairs Specialist to join them on an initial 6-month Fixed Term Contract. This is a fully remote position and can be based anywhere in the United...

Our client, a global pharmaceutical company, is currently looking for a Senior Regulatory Affairs Associate to join their team in Cambridge or West London (Uxbridge). This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their...

*No recruiters please*THE COMPANYWe are Regulatory Affairs experts who specialise in the UK and EU pharmaceutical industry and offer a bespoke consultancy service to our clients.Our first priority is to have a positive workplace culture where employees feel respected and valued. To achieve this, we only hire talented, dedicated and passionate individuals who...

Position Overview:We are seeking an experienced and driven Manager or Senior Manager, Regulatory Affairs specializing in Cell and Gene Therapy to join our team. This role will play a pivotal part in leading regulatory strategies and ensuring the successful approval and post-approval management of cutting-edge cell and gene therapy products. The Senior...

This job is with Autolus Therapeutics, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Role Summary With a significantly expanding regulatory team, an exciting opportunity has arisen for an experienced Senior Manager, Regulatory...

Senior Director Regulatory Affairs, Global Therapeutic Area HeadLocation: Candidate must have Right to Work in the UKRemote Working with International travel to HQ requiredAbout the company:We are working with a European biotech organisation, who are developing novel therapeutics for a range of rare diseases. They have achieved FDA success with a few of...

Regulatory Affairs Lead - Challenger BrandDriving Compliance Strategy - Rapid Growth CPG Co.Job DescriptionIf you’re an aspiring reg affairs leader with a passion for driving growth via delivery of expert compliance strategy, this is one for you!Reporting directly to the Head of Marketing / Innovation, this newly created role will see you take the lead in...

Regulatory Affairs Lead - Challenger BrandDriving Compliance Strategy - Rapid Growth CPG Co.Job DescriptionIf you’re an aspiring reg affairs leader with a passion for driving growth via delivery of expert compliance strategy, this is one for you!Reporting directly to the Head of Marketing / Innovation, this newly created role will see you take the lead in...

Director of Regulatory AffairsOur client, a global pharmaceutical company is seeking a Director of CMC Operations to lead and grow its CMC capabilities in Europe. This role will be pivotal in shaping early-stage drug development strategy, working across a diverse portfolio including small molecules, peptides, and macromolecules.About the Role:You will be...

A prominent organisation within the clinical trials sector, focusing on early-phase studies for pharmaceutical and biotechnology clients, is seeking a talented and experienced Head of Medical Writing and Regulatory Submissions. This role offers the opportunity to lead and manage teams within a dynamic, research-driven environment, dedicated to advancing...

This is a Senior Scientific Director role heading up a thriving publications account with some medical affairs. Applicants must already have significant experience working at SSD level in a MedComms agency setting.Roles at this incredible agency don't come up often so this is a rare opportunity to join this forward-thinking, truly independent healthcare...

Due to continued expansion we are currently seeking an additional Senior Regulatory Affairs Executive to join our team in a well-established Consultancy. You would have proven success in your current role and an ambition to continually develop together with commercial awareness, a drive to innovate and be a key part of a growing company in the pharmaceutical...