EU Regulatory Strategist

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...

Our client, a global pharmaceutical company is currently looking for a EU Regulatory Specialist to join their team based on the outskirts of London on a full time, 12-month temporary basis (35 hours per week).In this role, you’ll lead and manage the operational aspects of European regulatory filings, collaborating closely with European Regulatory groups...

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...

BH152140Content Strategist – Medical / Pharma Contract role – 6 months, extendableRate Guide = €550-600 per day (Ireland based) or £450-500pd (UK based)Location: UK based or Ireland based candidates only. NO SPONSORSHIP provided, so You MUST hold UK citizenship OR EU/EEA citizenship, or with existing full rights to work in Ireland or UK.Content...

Content Strategist - Remote (United Kingdom) - 3 to 6 months contract - £500 per day UmbrellaJob purpose:As part of Global Business Solutions, Creative and Digital provides in-house creative and multichannel marketing support to colleagues across client. With unique access to client-owned channels, the capabilities provide a seamless journey from concept...

Overview:A Quality and Regulatory team is seeking a full-time, permanent Regulatory Specialist to support the business in maintaining compliance with ISO 13485, Medical Device Directive 93/42/EEC, and Regulation (EU) 2017/745 (EU MDR).Key Responsibilities:Review, update, and create technical files, and conduct Post Market Surveillance activities for various...

Our client, a global pharmaceutical company which develops a portfolio of prescription generic and branded pharmaceuticals within the CNS, Neurology and respiratory areas. As Regulatory Affairs Manager, you will:Preparation, submission, and management of variation applications to agreed timelinesManage and submit Renewals and PSURs in line with specified...

My client a leading banking organisation are looking to hire a lawyer with 1-4 PQE experience in the regulatory space.This person could come from an inhouse role already or private practice.Desirable skills:Knowledge of key UK/EU regulatory regimes applicable to banks, funds and wealth managersAt the very minimum 1 PQE experience but ideally moreExperience...

Regulatory Labelling Contract:I’m working with a pharmaceutical company in the UK dedicated to improving healthcare as they look for a Freelance Labelling Contractor.Key Details:Fully remote role – anywhere in the EU6 to 12 month contractKnowledge of CCDS, EUspi and UspiKey Responsibilities:Prepare regulatory labelling packages in collaboration with the...

The client: A unique opportunity has arisen with a leading global insurance and reinsurance firm for a regulatory lawyer with an insurance sector coverage or commercial lawyer with regulatory experience.This individual will become a crucial member of the legal team, advising senior stakeholders across the business globally.Key responsibilitiesWorking as part...

An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...

We are seeking a skilled and experienced EU Energy Lawyer to provide legal expertise on complex energy projects and regulatory compliance for our Fortune 500 client! This is a full-time engagament through Epiq Counsel. IntroductionEpiq Counsel is an innovative legal services talent provider that offers meaningful work and flexibility to sophisticated and...

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. Job Title Director, UK & EU Compliance Officer Location: Remote or In Office, UK or EU based About Autolus Autolus is a clinical-stage...

*No recruiters please*Regulatory Affairs Consultant, Fusion Pharma THE COMPANYWe are Regulatory Affairs experts who specialise in the UK and EU pharmaceutical industry, we 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...

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...

Location: Hybrid role, London officeReports to: CEOCompany: Clinical trials stage biopharma company specializing in rare diseasesOverviewIQVIA are seeking an experienced Senior level Medical Affairs leader to join our client’s team, specialising in one specific rare disease area. Employed directly by the company in question (not on IQVIA contract), this...

Role: EMEA Regulatory Affairs ConsultantDuration: 5 MonthsLocation: High Wycombe, UK - Hybrid working (2 /3 days in High Wycombe office)KEY RESPONSIBILITIESManagement of post-approval activities for specified OTC products• Supports the EMEA Regulatory Affairs team for post-approval activities for MRP/DCP products across EEA and coordinate worksharing (WS)...

Title: Regulatory Affairs ManagerDuration: Till March 2024Location: Hybrid. 1 - 2 days in the office per week at High Wycombe HP12 4PTNotes: Inside IR35 - till March 2024 initially - OTC experience is essential.Job Description:EMEA REGULATORY AFFAIRS –REGULATORY CONSULTANTKEY RESPONSIBILITIESManagement of post-approval activities for specified OTC...

Head of Chemical RegulationsLocation - Hybrid/ Remote Options AvailableSalary - Negotiable & related to level of experienceOur client is an international Service Company, operating in over 80 countries. They Provide Heath & Wellbeing Products and Services that protect people’s lives and the reputation of their customers brands.We are seeking a Head of...

G&L is seeking a skilled, mid-level Regulatory Affairs CMC professional to support the authoring of various global post-approval CMC submissions for plasma protein therapeutic products. This role is solely focused on authoring the Chemistry, Manufacturing, and Controls (CMC) sections of the Common Technical Document (CTD). Our ideal candidate has experience...