Apply for Associate II Regulatory Operations at Alcon 2026. Check eligibility, experience, responsibilities, and last date to apply now.
Introduction
If you have experience in regulatory publishing and dossier submissions, this is a strong opportunity to advance your career. The Associate II Regulatory Operations at Alcon role is ideal for professionals with hands-on expertise in eCTD submissions, Veeva RIM tools, and global regulatory processes. This position offers exposure to international markets and end-to-end submission lifecycle management within a leading healthcare company.
Job Overview
| Job Title | Associate II – Regulatory Operations |
|---|---|
| Company Name | Alcon |
| Location | Bengaluru, India |
| Employment Type | Full-Time |
| Department | Regulatory Affairs / Regulatory Publishing |
| Experience Required | 3–4 Years |
| Education | B.Pharm / Life Sciences |
| Salary | As per company standards |
Company Overview
Alcon is a global healthcare company specializing in eye care products, including surgical and vision care solutions. With a strong presence worldwide, the company focuses on innovation, quality, and improving patient outcomes. Alcon provides a dynamic work environment with opportunities to work on global regulatory submissions and advanced healthcare solutions.
Job Location & Employment Type
This is a full-time position based in Bengaluru, India. The role requires collaboration with global teams and adherence to international regulatory timelines.
Open Positions / Department Details
The role is part of the Regulatory Operations and Publishing team. The department handles global dossier preparation, submission publishing, and compliance with regulatory authorities such as FDA, EMA, and other international agencies.
Key Roles & Responsibilities
- Prepare, compile, and publish regulatory dossiers for global markets (US, EU, RoW)
- Perform publishing activities for eCTD, NeeS, and paper submissions
- Manage submission lifecycle activities including sequence creation and amendments
- Conduct document quality checks to ensure accuracy and compliance
- Perform technical validation using regulatory publishing tools and resolve errors
- Coordinate with cross-functional teams for submission readiness and timelines
- Maintain submission records, metadata, and archives
- Ensure compliance with global regulatory standards (FDA, EMA, MHRA, etc.)
- Participate in process improvements and follow SOP guidelines
Eligibility Criteria
Education
- Bachelor’s degree in Pharmacy, Life Sciences, or related field
Experience
- 3–4 years of experience in regulatory publishing and submissions
Skills Required
- Strong knowledge of eCTD and NeeS submission formats
- Hands-on experience with Veeva RIM Publishing tools
- Familiarity with regulatory validators like Lorenz DocuBridge or Extedo eValidator
- Understanding of submission lifecycle management
- Good document review and quality check skills
- Strong communication and teamwork abilities
Salary & Benefits
- Salary: As per company standards
- Opportunity to work on global regulatory submissions
- Exposure to international health authority standards
- Career growth in regulatory operations and publishing
- Professional work environment with learning opportunities
Selection Process
The selection process may include:
- Resume screening
- Technical interview (Regulatory Publishing & Tools)
- HR discussion
How to Apply
Interested candidates can apply online through the official Alcon careers portal before the deadline.
Important Dates
- Last Date to Apply: April 22, 2026
Why Apply for This Job?
This role is highly valuable for professionals aiming to grow in regulatory affairs and publishing. It provides hands-on experience with global submissions, advanced tools like Veeva RIM, and exposure to international regulatory standards. Working at Alcon enhances your expertise and opens doors to senior roles in regulatory operations and global compliance.
FAQs
1. Who can apply for this job?
Candidates with a degree in Pharmacy or Life Sciences and 3–4 years of regulatory publishing experience can apply.
2. What tools are required for this role?
Veeva RIM Publishing tools and regulatory validators like DocuBridge or Extedo are required.
3. What is the job location?
The role is based in Bengaluru, India.
4. What is the last date to apply?
The last date to apply is April 22, 2026.
5. What type of submissions will I handle?
You will work on eCTD, NeeS, and paper-based regulatory submissions.
Conclusion
The Associate II Regulatory Operations at Alcon is an excellent opportunity for experienced professionals in regulatory publishing. With exposure to global markets and advanced submission tools, this role can significantly boost your career in regulatory affairs. Apply before the deadline to secure your chance.
Disclaimer
PharmaJobHub.in is an independent job information platform. We do not provide jobs or recruitment and are not affiliated with any company.
