EU Regulatory Affairs Specialist

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...

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...

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...

*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...

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...

Global household name speciality chemical companyResponsibility for National and Regional regulatory compliance Diverse business units – complex aqueous mixtures and substancesBecome a regulatory subject matter expert This will be a highly diverse role; typical duties include answering complex customer regulatory enquiries, researching/impact assessing...

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...

An opportunity to join the Chemical Regulatory science team at an R&D focussed global PPP company. We are looking for an:Ecotoxicology regulatory specialist 2-5 years industry experienceIdeally with aquatic knowledge and some experience of risk assessment. The role involves developing data, risk assessments and producing the ecotoxicology section of...

Our client, a global pharmaceutical company is currently looking for a EU Regulatory Strategist 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...

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 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...

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...

Company Overview:As a proud United Arab Emirates company based in Abu Dhabi, Medisal Pharma is dedicated to excellence in manufacturing high-quality pharmaceutical products. To support our expanding international operations, we are looking to hire a skilled Regulatory Manager to oversee our regulatory affairs and ensure compliance in the United Kingdom.Job...

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...

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...

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 Director, Regulatory Affairs to...

We have an opportunity for a Senior Scientific and Regulatory Affairs - UK/IRL Market Lead (known internally as - Program Manager SRA (Science & Regulatory Affairs) UK/IRL) to join us at Mars. You will lead a variety of regional regulatory activities related to raw materials, finished products, labelling, claims, packaging and supporting UK/IRL. In this...