Senior Regulatory Affairs Consultant
2 weeks ago
We’re looking for an experienced Senior Regulatory Consultant to join my client. The ideal candidate will have deep expertise in regulatory affairs for medical devices and digital health, with a focus on FDA and EU MDR, and experience managing submissions for Software as a Medical Device (SaMD).
Act as a regulatory expert on FDA, MDR, and other frameworks
Develop and execute regulatory strategies for digital health products
Guide clients through regulatory submissions and communications with authorities
Prepare regulatory documentation (e.g., Technical Files, Risk Management Files)
7+ years in Regulatory Affairs, specializing in medical devices and digital health
~ Bachelor’s degree required; SaMD and AI/ML regulatory frameworks
Digital health product development
At Life Sciences Recruitment Ltd (LSR), we are a Global Life Science recruitment firm that specialises in partnering with start-ups and fast-growing biotech and pharmaceutical organisations.
As one of the most competitive and fast-paced industries globally, succeeding and growing in the life sciences business requires a combination of creativity, technical expertise, and business savvy. At LSR, to find the best talent for your organisation, our dynamic recruitment consultants tap into our unparalleled network of contacts and apply a quality-based approach to a contingent search model tailored to your needs. We provide the most sought-after candidates to fit your requirements, from temporary placement to Fortune 500 companies
We are a subsidiary of Morgan Prestwich (MP), Europe's leading boutique Life Sciences executive search and advisory firm.
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