Medtronic · Hyderabad, India
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
This senior-level regulatory affairs position supports medical device design, development, and global registrations at a healthcare technology company. The role encompasses managing regulatory information systems, preparing international submission packages, maintaining compliance documentation, and collaborating with internal teams and regulatory agencies. Candidates should hold a relevant bachelor's degree and possess 7+ years of experience in medical device or pharmaceutical regulatory affairs.
This role links to Medtronic's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.
This role is listed from an approved source. RoleLantern checks that the application link is live and how recently the role appeared — the employer has not confirmed it directly on RoleLantern.
Upload your CV to see which of this role's requirements your background supports, where there may be gaps, and what needs clarification. Private by default — we never sell your CV.
See my match