We're currently partnering with a leading
Aumente sus posibilidades de conseguir una entrevista leyendo la siguiente descripción general de este puesto antes de presentar su candidatura.
global consumer health business
to find an experienced
Global Regulatory Operations Medicine Manager
to join their dynamic Regulatory Affairs team.
You'll be working at the heart of a fast-paced, innovation-driven environment, driving dossier strategy, managing global submissions, and collaborating closely with cross-functional teams across markets.
Oversee the planning, preparation, and timely submission of regulatory documentation (e.g., eCTD Modules 1–5) for product registrations, variations, renewals, and withdrawals, ensuring accuracy and compliance.
Collaborate Across Functions:
Work cross-functionally with Regulatory Strategy, R&D, Pharmacovigilance, Quality, and Marketing to ensure regulatory alignment throughout the product lifecycle.
Degree in Pharmacy, Life Sciences, or a closely related field (Bachelor's or Master's level).
At least 5 years of hands-on experience in regulatory affairs within the pharmaceutical or healthcare sector.
Solid track record in preparing and submitting eCTD dossiers, including CMC M3 content development. xohynlm