Description
ClinChoice is seeking a Regulatory Affairs Associate Consultant to work for a client for a 12-month contract with possible extension. The role is client-facing and involves preparing and submitting new registrations, changes, renewals, and establishment registrations; managing dossiers, labels, post-approval communications, audits, stakeholder interactions, compliance, INMETRO certification, and GMP activities. Candidates need 1–2 years of regulatory experience, preferably in medical devices or pharmaceuticals, a bachelor’s degree in engineering, pharmacy, or a related life science, strong English reading and writing skills, and fluency in Portuguese.
