Ad-Hoc Senior Regulatory Affairs Consultant

BaxMed – Ad-Hoc Senior Regulatory Affairs Consultant

Led by Stuart Baxter, a seasoned professional with a distinguished career in Regulatory Affairs, BaxMed Regulatory Ltd is an exciting early-stage organisation formed to provide Regulatory and Quality Compliance Services for the global Medical Device / healthcare sector. With a core ethos and commitment to simplifying the complexities of Regulatory Affairs, BaxMed offers a comprehensive range of services tailored to guide organisations to success in the highly regulated medical device and in vitro diagnostic space.

Role – Ad-Hoc Senior Regulatory Affairs Consultant

Brightwork is delighted to be supporting BaxMed as they seek to recruit an Ad-Hoc Senior Regulatory Affairs Consultant. Supporting a highly varied client base, start-up / early stage to well established, you will have a varied and interesting role providing support on an ad-hoc / as required basis, your role including;

• Working on dedicated client projects as a Regulatory Affairs Consultant
• Provision of comprehensive regulatory affairs support to a highly varied client base, predominantly within the Medical Device and related sectors
• Provide leadership and expertise in regulatory and submissions-related aspects for all elements of product development from initial concept through all design stages, through clinical trials to scale-up
• Providing technical support and guidance to clients in relation to Regulatory Affairs requirements, provisions and submissions
• Supporting delivery of submission-specific regulatory milestones

Ideally min degree qualified within a relevant discipline, you will be a highly experienced Regulatory Affairs Consultant / Specialist. You will be able to demonstrate a proven background in providing Regulatory Affairs support, guidance and management within a highly diverse client base – direct experience within the Medical Device and associated sectors is essential. This post will be offered on a remote on-going ad-hoc basis supporting BaxMed’s clients – travel to client sites may be required to meet business demands.

BaxMed Regulatory Ltd is poised to become a trusted name in the medical device sector, offering a full suite of services that span quality management systems, regulatory strategy development, in vitro diagnostic regulatory affairs, companion diagnostics regulatory affairs, medical device regulatory affairs and clinical affairs.

For further information on this excellent opportunity within an exciting early-stage organisation, please call Ian Grant on 07929 385 737 or email [email protected].