Senior Specialist Medical Device

IndiaIndia·Bangaloresenior
Other
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Quick Summary

Overview

Manage global regulatory product documentation, including technical files, registration dossiers, IFUs,

Technical Tools
Other
  • Manage global regulatory product documentation, including technical files, registration dossiers, IFUs, and labeling
  • Ensure compliance with regulatory standards and testing requirements throughout product design and development
  • Coordinate regulatory approvals and change notifications with Notified Bodies and Authorities
  • Ensure global regulatory product availability aligned with commercial strategy by managing registrations, renewals, and submissions
  • Coordinate regulatory product strategies
  • Lead regulatory aspects of product and process changes, including regulatory documentation.

Location & Eligibility

Where is the job
Bangalore, India
On-site at the office
Who can apply
IN

About this job

Who can apply
India
Posted
21 days ago
Employer
has 5,111 open jobs on Jobera in 41 countries.

Listing Details

First seen
September 29, 2026
Last seen
October 21, 2026

Posting Health

Days active
21
Repost count
0
Trust Level
17%
Scored at
October 21, 2026

Signal breakdown

freshnesssource trustcontent trustemployer trust
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Senior Specialist Medical Device