Apply for Specialist Regulatory Informatics job at Cencora 2026. Check eligibility, eCTD skills, salary, and application process details now online.
Introduction
The regulatory affairs domain is evolving rapidly with the integration of informatics and digital submission systems. The Specialist – Regulatory Informatics and Operations Job at Cencora presents an excellent opportunity for professionals with regulatory publishing and dossier experience to work in a global pharmaceutical environment.
This role is ideal for candidates who want to strengthen their expertise in eCTD submissions, regulatory operations, and informatics while collaborating with international teams.
Job Overview
| Particulars | Details |
|---|---|
| Job Title | Specialist – Regulatory Informatics and Operations |
| Company Name | Cencora (PharmaLex India Pvt. Ltd.) |
| Location | Noida, India |
| Employment Type | Full-Time |
| Department | Regulatory Affairs / Informatics |
| Experience Required | Minimum 3 Years |
| Education | B.Pharm / Science Degree (M.Pharm Preferred) |
| Salary | As per company norms |
Company Overview
Cencora is a global leader in pharmaceutical services, focused on improving healthcare outcomes for both humans and animals. Through its affiliated company, PharmaLex India Private Limited, Cencora delivers regulatory, compliance, and consulting services to pharmaceutical and biotech clients worldwide.
The company is known for its innovation-driven approach, strong global presence, and commitment to delivering high-quality regulatory solutions.
Job Location & Employment Type
This is a full-time position based in Noida, India. Candidates must be flexible to work in CET or US shift timings as required for global project coordination.
Open Positions / Department Details
The role is part of the Regulatory Informatics and Operations team, responsible for managing regulatory submissions, dossier publishing, and supporting global health authority requirements.
Key Roles & Responsibilities
- Support regulatory informatics and operations activities across Modules 1–5 of dossiers
- Handle pre-publishing, dossier compilation, publishing, and post-publishing processes
- Participate in regulatory submissions for multiple health authorities
- Work on US and EU eCTD submissions across different submission types
- Maintain strong client relationships and identify opportunities for additional support
- Contribute to regulatory informatics initiatives and digital submission strategies
- Ensure compliance with global regulatory standards and guidelines
- Collaborate with cross-functional teams for submission planning and execution
- Provide high-level support for regulatory documentation and publishing workflows
Eligibility Criteria
Education
- Bachelor’s degree in Pharmacy or any Science discipline
- M.Pharm is preferred for advanced roles
Experience
- Minimum 3 years of experience in regulatory affairs or publishing
- Hands-on experience in submission publishing, especially US submissions
Skills Required
- Strong knowledge of eCTD submission processes
- Experience with dossier modules (Modules 1–5)
- Familiarity with US and EU regulatory requirements
- Experience with publishing tools (mandatory)
- Knowledge of Veeva Vault (preferred)
- Good communication and client-handling skills
- Ability to work in global time zones
Salary & Benefits
- Salary: As per company norms
- Opportunity to work with a global pharmaceutical services leader
- Exposure to international regulatory frameworks
- Work on advanced regulatory informatics systems
- Career growth in regulatory affairs and publishing
- Inclusive and equal opportunity work environment
Selection Process
The recruitment process typically includes:
- Application screening
- Technical interview (Regulatory + Publishing knowledge)
- HR discussion
- Final offer
How to Apply
Candidates can apply through the official online application portal provided by the company. Ensure your resume highlights your experience in regulatory publishing, eCTD submissions, and tools like Veeva.
Important Dates
- Last Date to Apply: July 30, 2026
Why Apply for This Job?
The Specialist – Regulatory Informatics and Operations Job at Cencora offers a strong career path for professionals aiming to specialize in regulatory publishing and informatics.
Here’s what makes this role valuable:
- Work with global regulatory authorities (US & EU)
- Gain expertise in eCTD submissions and publishing
- Opportunity to work with advanced tools like Veeva
- Exposure to international pharmaceutical projects
- Strong career growth in regulatory operations
This role is particularly beneficial for candidates looking to advance in regulatory affairs, submission publishing, or regulatory technology domains.
FAQs
1. What qualification is required for this job?
Candidates must have a B.Pharm or science degree. M.Pharm is preferred.
2. What experience is needed?
At least 3 years of experience in regulatory publishing or operations is required.
3. Is Veeva experience mandatory?
Veeva experience is preferred but not mandatory. However, publishing experience is essential.
4. What type of submissions will I handle?
You will work on US and EU eCTD submissions across multiple modules.
5. Are shift timings required?
Yes, candidates should be flexible to work in CET or US time zones.
Conclusion
The Specialist – Regulatory Informatics and Operations Job at Cencora 2026 is a great opportunity for professionals seeking growth in regulatory publishing and informatics. With global exposure, advanced tools, and strong career prospects, this role is ideal for experienced candidates in regulatory affairs.
Apply early to take advantage of this opportunity and advance your career in the pharmaceutical industry.
Disclaimer
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