Employment Type : Full-Time
Regulatory Affairs Specialist, RA Specialist, FDA, 510(K), SaMD, Remote, COR5716 The Role This is an excellent Regulatory Affairs Specialist / RA Specialist, working for a company with a growing reputation in their field. The successful Regulatory Affairs Specialist / RA Specialist will have hands-on knowledge of FDA regulations, ISO standards & SaMD - as well as proven experience working with medical devices that use AI & Mach...
Employment Type : Full-Time
Senior Regulatory Specialist Cardiff 40,000 - 50,000 Yolk Recruitment is partnered with a pioneering medical device business during an exciting period of sustained expansion and has a new opportunity for a Regulatory Specialist to join the team. The role offers not only the opportunity to be a part of a high growth, high innovation business in a rewarding field, but to make your mark in a lead role providing guidance on a wide range of regulator...
Employment Type : Full-Time
Senior Regulatory Specialist Cardiff CF14 40-50,000 Commutable from Cardiff, Newport, Bridgend, Caerphilly, Barry, Llantrisant, Pontypridd Benefits:- Highly competitive salary Bonus Opportunity 25 Days Bank Holidays Employee assistance programme Matched 5% pension Funded company social events Free on-site parking and secure cycle shelter Discounts at local restaurant and local gym Are you an experienced Regulatory Affairs professional? This coul...
Employment Type : Full-Time
My client, a forward-thinking medical device company at the forefront of bioelectronic medicine. Their mission is simple, they're set to revolutionise healthcare by developing cutting-edge therapies for individuals battling chronic diseases. With their breakthrough, they have been granted the Breakthrough Device Designation by the United States FDA, enabling accelerated market access for devices addressing life-threatening or irreversibly debili...
Employment Type : Full-Time
Senior Regulatory Specialist - Biocides - Hybrid/Remote Are you a Senior Regulatory Specialist / Regulatory Affairs Manager who would you like to work with a fast-growing business with lots of technical development planned for the next 3 years?? The role of Senior Regulatory Specialist offers you the chance to work with a globally recognised business with a strong client base who are even having to currently turn down work! The successful Senior...
Employment Type : Full-Time
We are seeking a talented Regulatory Affairs Specialist to join our client's regulatory team in support of the expansion of their ISO 13485 diagnostics product pipeline. Reporting to the Regulatory Affairs Manager, you will play a crucial role in ensuring regulatory compliance and supporting the successful submission of our products to global regulatory agencies. As Regulatory Affairs Specialist responsibilities include: * Collaborate closely wi...
Employment Type : Full-Time
We are currently looking for a Regulatory Affairs Specialist to join a leading Distribution company based in the Kent area. As the Regulatory Affairs Specialist you will be responsible for maintaining the integrity and compliance of medicinal product imports, ensuring the highest standards are met in line with industry regulations. This will be a hybrid role consisting of 3 days on site and 2 days working from home. KEY DUTIES AND RESPONSIBILITI...
Employment Type : Full-Time
We are looking for a regulatory affairs professional to join a chemical products manufacturing business. Key elements of the role include regulatory research and analysis, maintenance of key chemical regulatory documents, compilation of regulatory dossiers to support product approval globally and, authoring and maintenance of safety data sheets. This is a challenging and diverse role within a friendly regulatory team that offers excellent career...
Employment Type : Full-Time
TEC Partners is pleased to have partnered with a pioneering medical device company who is set to pave the way for AI-based automated analysis software to overcome a global crisis affecting millions of lives. Quality and Regulatory Specialist As the Quality and Regulatory Specialist, you will play a pivotal role in my client's mission to deliver groundbreaking solutions in global diagnostics. Your key responsibilities will include document contro...
Employment Type : Full-Time
Summary Thanks for checking out our vacancy, we're delighted you want to learn more about Dechra. Dechra are a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide. Here at Dechra, our values are embedded within our culture and thrive within our family of almost 2500 colleagues globally. Fro...