They are searching for a regulatory affairs professional to join them in tackling important sector challenges, ensuring they stay ahead of industry risks.
A great opportunity to work with a leading and trusted organisation.
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.
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.
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.
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.
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.
The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials.
They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes.
General
SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote.