PHARMAFull-time
Regulatory Operation - Publishing & Registration
BANGALORE (India)ONSITEPOSTED: 9/21/2026
PHARMAFull-time
HIRING ORGANIZATIONALCONMedical Devices and Eye Care
ROLE OVERVIEW
Regulatory Operations role focused on submission-ready document formatting, regional regulatory publishing, registration package preparation, and controlled regulatory documentation.
ROLE DEFINITION & RESPONSIBILITIES
- •Apply submission-ready formatting and ensure template compliance
- •compile regulatory submission packages according to US, EU, and Canada requirements
- •render PDFs with bookmarks, hyperlinks, and cross-references
- •operate Veeva RIM Publishing tools
- •draft Powers of Attorney and Letters of Authorization
- •prepare Free Sale Certificates and request CFG-NE where eligible
- •populate controlled templates with version control
- •cross-map documents across eSTAR, IMDRF ToC, and MDR requirements
Reporting Hierarchy: Reporting structure is not explicitly stated; role operates within Alcon regulatory operations and publishing/registration activities.
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Regulatory operations knowledge
- document formatting and publishing skills
- ability to follow controlled templates and version-control procedures
- familiarity with regulatory submission documentation
- attention to detail and document quality
PREFERRED QUALIFICATIONS
- •Experience with Veeva RIM Publishing
- •knowledge of US, EU, and Canada regulatory submission formats
- •familiarity with eSTAR, IMDRF Table of Contents, and MDR
- •experience preparing POA, LOA, FSC, or CFG-NE documentation
REQUIRED VERIFIED SKILLS
Regulatory publishing
document formatting
submission preparation
Veeva RIM Publishing
PDF publishing
template compliance
version control
regulatory documentation
cross-referencing
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Company benefits not specified in the provided posting; role provides exposure to regulatory publishing, registration, and global submission operations
Salary is not stated in the provided posting; no salary figures are inferred.
ORGANIZATION CONTEXT & CULTURE
Alcon is a global eye care company focused on developing and delivering products and technologies for eye care professionals and patients.
TEAM SIZE: Large global organization
INDUSTRY: Medical Devices and Eye Care
Culture: Diversity-focused, inclusive, compliance-oriented, and quality-driven.
EXPECTED CAREER ROADMAP
Potential progression into Regulatory Operations, Regulatory Publishing, Regulatory Submission Management, or broader Regulatory Affairs roles.
APPLICATION ADVISORY
Emphasize regulatory document publishing, submission formatting, Veeva RIM experience, controlled-document practices, version control, and knowledge of regional regulatory requirements. Highlight accuracy and attention to detail.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.