EMEA Principal Regulatory Affairs Lead

A global healthcare company seeks a Principal Regulatory Affairs Specialist to lead regulatory support in the UK&I, BeNeLux, and Nordic regions. The ideal candidate will have 6-8 years of medical device regulatory experience and technical writing skills. Responsibilities include reviewing regulatory documents, ensuring compliance, and mentoring junior team members. The role offers competitive compensation and extensive training opportunities for career growth.#J-18808-Ljbffr…