Regulatory Affairs Specialist 2

Supports implementation of regulatory strategies for smaller, less complex projects by collaborating with regulatory and cross-functional SMEs. Assists in preparing and coordinating product submissions, conformity assessments, and change control processes. Reviews labeling, marketing communications, and development quality reports to ensure regulatory compliance.

Bachelor's Degree / Vocational Education in Biomedical Engineering, Business Administration, Health Sciences, Pharmaceutical, Law or equivalent. No prior experience required with bachelor's degree OR minimum 4 years of experience with Vocational Education in Regulatory Affairs, Quality Compliance, Product Development in Medical Devices Industry or equivalent. Ability to fluidly communicate in English is required.

This role is an office role with Administrative shift. For office-based teams, working in-person at least 3 days per week is required.