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.
We are currently looking for a Regulatory Affairs Specialist to join a leading Distribution company based in the Kent area.
This will be a hybrid role consisting of 3 days on site and 2 days working from home.
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.
They are searching for a regulatory affairs professional to join them in tackling important sector challenges, ensuring they stay ahead of industry risks.
This individual will be critical in contributing to major sector reforms and conversations, from product health and safety to the organisation's contribution to climate change.
A great opportunity to work with a leading and trusted organisation.
We are seeking a Quality Assurance / Regulatory Affairs Officer to support this global medical device company in meeting its quality and regulatory requirements.
Provide technical support for medical device manufacturing, engineering, and distribution.
Do you have quality assurance and regulatory affairs experience within the medical devices sector?
An excellent role on offer for an individual with quality assurance and regulatory experience within the medical sector looking to play a key role at an industry leading company.
Would you like to work for a world leading company?
An opportunity has now become available for an experienced Regulatory Affairs Manager to join the company and undertake a leading role in product compliance with industry standards and regulatory requirements.
As a fully regulatory compliance facility, our client are able to provide technical innovation supporting with the formulation and development of novel cleaning products across many sectors.
Our client is an established contract manufacturing organisation (CMO) providing services on a global scale.
WE Talent are working with a regulatory business in the City of London who are recruiting for a Policy and Regulatory Standards Officer to join their team.
This is an ideal role for an experienced Policy and Regulation expert who is looking for a role where you will have autonomy and work closely with the Head of Policy and leadership team.
Responsibilities will include
Project manage policy projects and reviews, drafting policy options and making recommendations.
Regulatory Affairs Specialist, RA Specialist, FDA, 510(K), SaMD, Remote, COR5716
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.
This is an excellent Regulatory Affairs Specialist / RA Specialist, working for a company with a growing reputation in their field.