Help bring innovative medical technologies to patients by driving regulatory excellence across the product lifecycle. In this role, you will shape registration strategies, navigate evolving regulatory landscapes, and ensure compliant, timely access to life‑changing devices. If you thrive in a fast‑moving environment where your expertise directly impacts market success, this is an exciting opportunity to make a meaningful difference.

What you will do

+ Prepare, coordinate, and submit regulatory applications to local health authorities to support timely product approvals.
+ Compile and complete regulatory submission dossiers including new products, line extensions, amendments, updates, renewals, and change notifications in accordance with applicable regulations and guidance.
+ Evaluate products for regulatory classification and determine appropriate submission pathways to enable efficient market access.
+ Monitor local regulatory changes, assess impact, and imp...