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Following recent expansion, they are seeking a Regulatory Officer to join their Regulatory team. Regulatory Affairs Officer - Beauty. Request and organise key regulatory documents such as INCIs, MSDSs, and compliance certificates.

Preparing and compiling regulatory documentation, coordinating and executing regulatory submissions in compliance with ISO13485, IVD 2017/746 Regulation, FDA 21 Code of Federal Regulations (CFRs), Biologics License Applications (BLA), Medical Device Approvals (510(k)), Canadian Medical Device Reg...

Company OverviewRainbird Technologies is a pioneering leader in Decision Intelligence, delivering "AI the world can trust." Founded in 2013, we are revolutionising how organisations make complex decisions through our no-code platform that combines extended knowledge graphs, symbolic r...

Quality Assurance and Regulatory Affairs Lead. A London based Start-up Medical Device company developing a Class 1 Measuring Device is on the look out for a Quality and Regulatory Lead to join their growing business. Developing and executing regulatory strategies for FDA clearance, followed by ot...

Role:Chief Financial Officer Location: London, UKContract:Full-time, PermanentReporting Line:CEOPTW is seeking a veteran Chief Financial Officer (CFO) to join our executiv...

Stay ahead of regulatory trends and ensure compliance with evolving standards. Are you an experienced regulatory professional ready to take the lead in shaping innovative CMC strategies? Barrington James is recruiting for a. If you’re passionate about guiding clients through complex regulatory la...

Reporting directly to the Global Head of Regulatory, you will play a pivotal role in ensuring regulatory approval across a diverse pipeline of assets. Senior Director Regulatory Affairs, Global Therapeutic Area Head. This role is an exciting opportunity to join as Senior Director Regulatory Affai...

Participate in the regulatory meetings with internal or external clients  Co-ordinate and provide regulatory support to the licensing partners in the respective territories for post approval regulatory activities. Liaise and follow up with regulatory authorities submissions and regulatory issues...

Senior Risk ActuaryLondon - Hybrid (50/50)Role Overview:My client, a prestigious BPA provider, is seeking a highly skilled Senior Risk Actuary to join our wider Risk department. The Risk department plays a critical role in e...

You will be enthusiastic, highly motivated, have a strong work ethic and be well-equipped to work closely with the other members of the Legal Department on the types of matters described below in addition to other matters that may arise. About the Team:The Legal Dep

Role: Chief Financial OfficerLocation: London, UKContract: Full-time, PermanentReporting Line: CEOPTW is seeking a veteran Chief Financial Officer (CFO) to join our executive team. The CFO will play...

We are Regulatory Affairs experts who specialise in the UK and EU pharmaceutical industry and offer a bespoke consultancy service to our clients. We continue to grow and are delighted to be recruiting for our next member of the team in the Regulatory Affairs Department. Update to Regulatory track...

Utilize regulatory tools and databases to streamline operations and ensure regulatory deliverables are met. As we expand our footprint, we are on the lookout for passionate and skilled Regulatory professionals to join us in shaping the future of regulatory services. Candidates should be equipped ...

Support the Director, Global Clinical Affairs in implementing the vision for Clinical Affairs to drive the quality, cost, speed, and efficiency of clinical studies delivery. Clinical sites: selection, contract development, budget negotiation, and monitoring; recruitment; regulatory and ethics sub...

Experience and qualifications for the Compliance & Licensing Specialist – Government and Regulatory Affairs::. Licensing Specialist – Government and Regulatory Affairs. Key Responsibilities for the Compliance & Licensing Specialist – Government and Regulatory Affairs:.

An individual contributor position in Regulatory Affairs Operations responsible for supporting the implementation of Regulatory Records Management (categorizing and classifying information) related to the client’s product portfolios and Mergers, Acquisitions and Divestment (MA&D) activities. Resp...

Regulatory Affairs Manager, Market Access Strategy. Market Access Strategy Manager. Global Regulatory Affairs team.

Senior Regulatory Affairs Associate.West Lothian ~ remote working available but hybrid preferred.After an incredible 12 months of working towards FDA approval and opening overseas manufacturing sites, this Scottish born medical device company are going global due to demand for their product.As pa...

As a Regulatory Consultant, your expertise is instrumental in helping them navigate the complex landscape of global submissions, ensuring compliance with MDR, IVDR and FDA requirements. Leading regulatory submissions, including EUMDR and EU IVDR, US FDA 510(k)s, PMAs, IDEs, and global market appr...

We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, Risk Assessment, Regulatory Toxicology, Regulatory Ecotoxicology and Environmental Fate in the chemicals, agrochemicals and biocides sectors. We are looking for a chemical regulato...

You will serve as the primary point of contact for internal teams and external sponsors, providing strategic advice on regulatory affairs and medical writing. Lead recruitment efforts for the medical writing team, ensuring clear career progression and succession planning. Medical Writing Responsi...

An individual contributor position in Regulatory Affairs Operations responsible for supporting the implementation of Regulatory Records Management (categorizing and classifying information) related to company product portfolios and Mergers, Acquisitions and Divestment (MA&D) activities. Looking f...

The Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory res...

An individual contributor position in Regulatory Affairs Operations responsible for supporting the implementation of Regulatory Records Management (categorizing and classifying information) related to the product portfolios and Mergers, Acquisitions and Divestment (MA&D) activities.Under the supe...