If you’re looking for Regulatory Publisher jobs in Mumbai, Piramal Pharma is hiring a Regulatory Publisher for its Piramal Critical Care (PCC) division. This is an excellent opportunity for life science graduates interested in Regulatory Affairs, eCTD publishing, electronic submissions, FDA submissions, and EU regulatory documentation within the pharmaceutical industry.
Professionals with strong attention to detail and an interest in global regulatory operations can build a rewarding career supporting submissions to international health authorities.
About Piramal Critical Care
Piramal Critical Care (PCC), a business unit of Piramal Pharma, is among the world’s leading manufacturers of inhaled anesthetics and hospital generic medicines. The company serves healthcare providers across the United States, Europe, and more than 100 countries.
Its manufacturing facilities are regularly inspected by global regulatory agencies, including the US FDA and UK MHRA, ensuring compliance with international quality standards.
Job Details
| Details | Information |
|---|---|
| Position | Regulatory Publisher |
| Company | Piramal Pharma โ Piramal Critical Care |
| Location | Mumbai, Maharashtra |
| Work Mode | Hybrid (Onsite) |
| Employment Type | Full-Time |
| Department | Regulatory Affairs |
| Application Deadline | July 30, 2026 |
Key Responsibilities
As a Regulatory Publisher, you will:
- Prepare and compile regulatory submission documents.
- Publish electronic submissions in eCTD format.
- Support submissions to the US FDA, European Union, and other global health authorities.
- Review regulatory documents for publishing accuracy.
- Ensure compliance with global regulatory publishing standards.
- Coordinate with Regulatory Affairs teams during submission activities.
- Maintain submission quality and document integrity.
- Follow internal SOPs and regulatory guidelines.
- Assist in electronic lifecycle management of regulatory dossiers.
Required Qualifications
Candidates should have:
- Bachelor’s degree in Science (BSc) or a related Life Sciences discipline.
- Good understanding of Regulatory Affairs.
- Knowledge of eCTD publishing and electronic submissions.
- Familiarity with FDA, EMA, or other international regulatory requirements.
- Strong documentation and organizational skills.
- Excellent attention to detail.
- Good communication skills.
- Ability to work in cross-functional global teams.
Preferred Skills
- Regulatory Publishing
- Electronic Submissions
- eCTD
- FDA Submission Process
- EMA/EU Regulatory Documentation
- Document Publishing Tools
- Pharmaceutical Regulatory Affairs
- Digital Publishing
- Regulatory Compliance
- Life Sciences Documentation
Why Join Piramal Pharma?
Working at Piramal Pharma offers:
- Opportunity to work on global regulatory submissions.
- Exposure to FDA and European regulatory systems.
- Hybrid working environment.
- Career growth in Regulatory Affairs.
- Collaborative international teams.
- Learning opportunities in pharmaceutical compliance.
- Stable organization with a global presence.
How to Apply
