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 with the Regulatory Affairs Manager to develop and maintain technical files and submissions for global regulators.
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 development.
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 & Machine Learning.
Regulatory Affairs Specialist, RA Specialist, FDA, 510(K), SaMD, Remote, COR5716
This is an excellent Regulatory Affairs Specialist / RA Specialist, working for a company with a growing reputation in their field.
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 regulatory affairs.
As a Regulatory Affairs Executive, your role will be instrumental in supporting the administrative backbone of the department, maintaining the precision of the regulatory database, and orchestrating the preparation and tracking of regulatory submissions across various stages.
Are you looking for a new opportunity where your expertise will be pivotal in navigating the complexities of UK/EU regulatory frameworks?
Based in Berkshire, this role offers the chance to become an integral part of a leading Pharmaceutical company, ensuring that innovative health solutions reach the market efficiently and safely.
A Regulatory Specialist is urgently required or the responsibility of providing global regulatory and scientific support for new and existing products, raw materials and processes.
We are looking to hire a candidate strongly interested in Regulatory Affairs - with experience in medicinal products.
The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position available to build Medicinal Product capability in and outside Europe.
You will grow and maintain major portfolio in particular for the European region, you will coordinate changes to existing products/dossiers keeping them on the market.
We are looking to hire a Regulatory Specialist permanently for a Medical Device manufacturer taking full ownership for their biocide product range.
If you've been looking for a company allowing you to work remotely, this is it.
Here's a sneak peek into what your role will entail
Technical documentation: You will be responsible for maintaining and updating technical documentation, ensuring compliance with regulations such as MDD to MDR (Medical Device Regulation).
Global Regulatory Affairs - Due Diligence Manager / Senior Manager
This US Biotech are looking for a Regulatory Affairs professional with strong Due Diligence experience to join an exciting, high-profile project, this is initially a 6 month contract but has scope for extension.