Alcon has announced an opportunity for Regulatory Operations – Regulatory Data Management in Bangalore, India. The position is part of Alcon’s Quality & Regulatory Affairs function and involves regulatory data management, compliance activities, submission operations, data quality, reporting, reconciliation, and workflow automation.
Candidates interested in regulatory affairs jobs, regulatory operations jobs, regulatory data management, pharmaceutical regulatory careers, medical device regulatory affairs, and GxP compliance roles can consider this opportunity.
Alcon Regulatory Operations Job Details
| Particular | Details |
|---|---|
| Company | Alcon |
| Position | Sr. Associate, Regulatory Operations – Regulatory Data Management |
| Location | Bangalore, India |
| Job Type | Full-time |
| Experience | Relevant education and experience required |
| Function | Quality & Regulatory Affairs |
| Requisition ID | R-2026-49014 |
| Application Deadline | September 22, 2026 |
| Work Mode | Remote type not applicable |
About Alcon
Alcon is a global eye-care company focused on developing products and technologies that help people see brilliantly. The company operates across medical devices and pharmaceutical products and has more than 25,000 associates.
The Regulatory Operations position supports Alcon’s Quality & Regulatory Affairs organization, helping ensure regulatory compliance and effective management of regulatory data and documentation.
Regulatory Operations – Regulatory Data Management Responsibilities
The selected candidate will be responsible for activities related to regulatory operations and regulatory data management, including:
- Manage regulatory data entry, maintenance, and registration hierarchy.
- Perform data quality and validation checks at the point of collection.
- Define and monitor KPIs such as cycle time, first-pass yield, and on-time renewals.
- Monitor performance metrics and identify trends over time.
- Monitor regulatory dashboards and reports.
- Automate data workflows and trackers using PowerApps and Power Automate.
- Perform data reconciliation and resolve discrepancies.
- Support Change Control, Audit Management, and Quality Metrics activities.
- Review regulatory documents for accuracy and compliance.
- Support dossier preparation and regulatory submission activities.
- Handle Clinical Trial Disclosure and submission management activities.
- Support submission publishing, licensing, and labeling processes.
- Maintain accurate databases of regulatory submissions and approvals.
- Conduct independent research and specialized regulatory tasks.
- Follow applicable GxP regulations, SOPs, quality procedures, and documentation requirements.
- Contribute to continuous improvement and organizational compliance.
Key Skills for Alcon Regulatory Data Management Jobs
Candidates applying for this Alcon regulatory operations job should have knowledge or experience relevant to areas such as:
- Regulatory Operations
- Regulatory Data Management
- Regulatory Affairs
- Data Entry & Data Maintenance
- Data Validation
- Data Reconciliation
- Submission Management
- Regulatory Databases
- Change Control
- Audit Management
- Quality Metrics
- KPI Reporting
- Dashboard Monitoring
- GxP Compliance
- SOP Compliance
- Clinical Trial Disclosure
- Submission Publishing
- Licensing and Labeling
- Microsoft PowerApps
- Microsoft Power Automate
- Data Workflow Automation
Qualifications
Regulatory Compliance at Alcon
The role requires adherence to GxP regulations and Alcon’s established Standard Operating Procedures.
The selected candidate will be expected to:
- Maintain accurate and complete documentation.
- Follow applicable SOPs.
- Perform required quality-control activities.
- Complete mandatory training.
- Support regulatory and organizational compliance.
- Participate in continuous-improvement initiatives.
Benefits & Career Opportunity
The job posting highlights Alcon’s focus on an inclusive working environment and opportunities for associates to develop their careers.
Potential career exposure through this role includes:
- Regulatory Operations
- Regulatory Data Management
- Quality & Regulatory Affairs
- Regulatory Submission Management
- Medical Device and Pharmaceutical Compliance
- Data Analytics and KPI Management
- Regulatory Workflow Automati
Who Can Apply?
This opportunity may be relevant to professionals with backgrounds in:
- Regulatory Affairs
- Regulatory Operations
- Regulatory Data Management
- Pharmaceutical Sciences
- Pharmacy
- Life Sciences
- Clinical Research
- Medical Devices
- Quality Assurance
- Drug Regulatory Affairs
Candidates should carefully review the official Alcon posting for the exact education and experience requirements applicable to the role.
How to Apply
