Senior Director Regulatory Affairs

Join the regulatory affairs team at a global pest control products company. Friendly and experienced team Work on compliance and registrations for a global portfolio of products. Duties will be varied and will include biocide product registrations / notifications, gathering data, compiling dossiers, liaison with testing teams, SDS authoring, classifications,...

Global Healthcare Company currently seeks a Regulatory & Quality Director to join their team based in Surrey. The Regulatory & Quality Director leads a team of technical, regulatory, and quality specialists, to ensure compliance for all regulated activities. This is a broad remit which includes responsibility for government relations, issue management,...

Associate Director (Regulatory Affairs)My client are a dynamic and innovative medical technology company focused on developing advanced healthcare solutions. As we navigate through the transition to the Medical Device Regulation (MDR), we are seeking a highly skilled and experienced professional to join our team as Associate Director of Regulatory...

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

Regulatory Affairs Specialist - Lifecycle MaintenanceLocation: RemoteWe are seeking an experienced Regulatory Affairs Specialist to oversee lifecycle maintenance for our mature product portfolio. The successful candidate will manage compliance activities, coordinate with EU member states under the MRP, handle national product regulations, and ensure all...

Group Director of Regulatory ComplianceLondonBoston Link's client, a prominent company in the online gambling and entertainment industry, is seeking an experienced Director of Compliance and Regulatory Affairs to join their team. The successful candidate will play a crucial role in embedding and refining the compliance framework, focusing on team management,...

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...

Senior Regulatory Affairs Specialist - Medical Device Main Purpose of Job and Objectives:Perform Regulatory tasks to ensure compliance with regulations.Prepare regulatory documentation and submissions for product approvals.Develop regulatory plans/strategies for new products and changes to existing products.Participate in Design Control and Risk Management...

Job Title: Senior Regulatory Affairs and Clinical LeadJob Type: Full-time, permanent positionLocation: West Oxfordshire, (On-site) Remuneration: £100,000 +This is an excellent opportunity to join a leading medical device manufacturing that is the world leader in Glucose Monitoring, their ranging product portfolio, develops and manufactures glucose...

Regulatory Affairs Custom Device Team Lead / Senior Regulatory Affairs Custom Device AssociateMain Purpose of Job and Objectives:Perform Regulatory tasks to ensure compliance with regulations.Prepare regulatory documentation and submissions for product approvals.Develop regulatory plans/strategies for new products and changes to existing products.Participate...

Regulatory Affairs Advisor (French Speaking)At Campden BRI, we have a dedicated Regulatory Affairs Team who offer a valuable and expert advisory service, as we're the leading authority, helping our clients stay compliant with food regulations in more than 80 countries! We are widely recognised for our expertise in the interpretation and commercial...

The business provides scientific, technical, and legislative support to the food and beverage industries worldwide. About the Regulatory Affairs Advisor jobThe purpose of your role will be to ensure provision of safe, honestly marketed food meets legal, commercial and moral standards. Key tasksMaintain and extend a high level of awareness of current food...

I am working with a growing pharmaceutical company who provide over-the-counter (OTC) pharmaceutical products dedicated to enhancing the health and well-being of customers. They're currently in the next phase of growth for the company as they're overtaking a consumer portfolio from a huge company in the pharmaceutical industry.....Position Overview: We are...

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...

Leading independent strategic communications consultancy looking for Public Affairs Account Executive / Senior Account Executive to join their growing team.Headquartered in London with global offices, the agency works with clients across a range of sectors including:Financial servicesFintechEnergyReal EstateTechnologyThey are expanding their public affairs...

Senior/Principal EU Regulatory Consultant - RemoteNAMSA pioneered the industry and was the first independent company in the world to focus solely on Medical Device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976.We are shaping the industry. NAMSA has been a key...

We are looking for UK-based senior business lawyers who are qualified in England & Wales with significant in-house experience and at least 10 years PQE.Selling legal services in a way that no-one else does, The Legal Director provides businesses with high-calibre, experienced lawyers on a part-time and/or flexible basis. The Legal Director is ideal if you...

BioTalent are working with a Global Consultancy business in their search for an Associate Director Regulatory Labelling for a 12 month contract. Candidates must have at least 8 years of experience in:An exclusively labelling focussed role (not regulatory roles which include aspects of labelling)Labelling strategyCCDS creation and maintenance End-to-end...

SENIOR MEDICAL WRITER (Germany, UK, USA, Canada, Portugal, Italy, Ireland)Only candidates who meet the following requirements will be considered:Candidate must live in one of the following countries: Germany, UK, USA, Canada, Portugal, Italy, Ireland. Applicants will work from one of our offices (Frankfurt, Germany; Cambridge, UK; Durham, NC, USA) or...

Our client is a global pharmaceutical brand who are expanding their programming and statistical teams. They are currently looking for senior level (and above) programmers who will be engaged on inital 12 month contracts on a fully remote basis.Programming is the department that oversees and delivers the programming aspects of clinical drug development,...