Flexible Hybrid Regulatory Specialist Jobs

We are looking for an experienced Regulatory Affairs Consultant to support MDR transition, risk management, and validation documentation activities within a highly regulated pharmaceutical/medical device environment. This 12‑month hybrid assignment is based in Antwerp, working 2-3 days on‑site. Key ResponsibilitiesUpdate and rewrite Risk Management...

A key client of EPM Scientific is seeking a Sr. Regulatory Affairs Specialist to join their team on a 12 month contract, supporting primarily around Regulatory Submissions & Intelligence in their Joint Replacement Orthopaedics division.This is a full time role, ASAP start, hybrid on site in Southern Ireland (negotiable).Assesses Regulatory Intellig...