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 guidanc...