Piramal Pharma Regulatory Publisher Jobs 2026 | eCTD Publishing & FDA Submissions Jobs in Mumbai
Are you seeking Piramal Pharma Careers or a Regulatory Affairs Job in Mumbai? Piramal Pharma's specialized division Piramal Critical Care (PCC) is hiring a Regulatory Publisher (Job ID: R00002345) for its Regulatory Operations department.
This electronic dossier publishing vacancy is ideal for science, pharmacy, or life science graduates with 0 to 3 years of experience in eCTD formatting, FDA document compiling, and electronic regulatory submissions. To write a resume detailing your regulatory archiving or document formatting milestones, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | Piramal Pharma – Piramal Critical Care |
| Position | Regulatory Publisher |
| Job ID | R00002345 |
| Job Location | Mumbai, Maharashtra, India |
| Work Mode | Hybrid (Onsite) |
| Department | Regulatory Affairs / Operations |
| Experience Required | 0–3 Years (Freshers & Juniors) |
| Qualifications | Bachelor of Science (BSc), B.Pharm, or related Life Sciences degree |
| Application Deadline | July 30, 2026 |
💼 Key Responsibilities
- Dossier Compilation: Assist in the preparation, compiling, and reviewing of regulatory dossiers and electronic submissions.
- eCTD Publishing: Format, build, and publish electronic applications in eCTD format for health authorities.
- Global Filings: Support electronic filings and lifecycle submissions to the US FDA, European Union (EMA), and other global regulators.
- Document Review: Verify document hyperlinking, bookmarking, and formatting to ensure publishing quality standards are met.
- Regulatory Compliance: Ensure all dossiers follow global health authority guidelines and internal SOPs.
- Lifecycle Tracking: Support the archiving and electronic tracking of regulatory communications.
To learn how regulatory publishing salaries compare to conventional pharmacovigilance drug safety associate and clinical data management structures, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Education: Bachelor of Science (B.Sc.), B.Pharm, or equivalent Life Science degree.
- Experience: 0 to 3 years of experience. Freshers with certified training in Regulatory Affairs/eCTD are welcome to apply.
- Technical Knowledge: Familiarity with eCTD formatting, PDF compilation, XML validation, and electronic submission tools.
- Attention to Detail: Strong document formatting and quality verification skills.
- Communication: Good written and verbal English communication, working alongside international regulatory leads.
For science graduates evaluating regulatory affairs careers compared to laboratory quality control or sales tracks, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Piramal Critical Care?
- Work for a global hospital generics leader supplying products to over 100 countries.
- Hands-on experience compiling dossiers for major agencies like the US FDA and UK MHRA.
- Modern hybrid work model combining home flexibility and office collaboration.
- Structured career ladder in global regulatory operations.
To review your basic knowledge of drug trial phases, regulatory definitions, and GCP parameters before your technical interviews, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Regulatory Publishing vs Healthcare IT
Regulatory Publishers prepare electronic submissions, build eCTD dossiers, and ensure compliance with FDA guidelines, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Piramal Regulatory Candidates
- Feature eCTD Software: Mention specific eCTD compilation or validation software (like docuBridge, eCTDmanager, or Lorenz) if you have used them.
- Detail Document Formatting: Highlight your skills in advanced PDF bookmarking, hyperlinking, and rendering documents compliant with FDA specifications.
- State Regulatory Training: If you did an internship, thesis, or certificate course on Drug Regulatory Affairs (DRA), describe it clearly.
💬 Piramal Regulatory Publisher Interview Questions
- Q1. What are the five modules of an eCTD (electronic Common Technical Document)?
Answer Guidance: Module 1 contains administrative and regional information. Module 2 contains the summaries and overviews. Module 3 details quality and chemistry (CMC). Module 4 contains non-clinical study reports, and Module 5 contains clinical study reports. - Q2. Why is document formatting (like bookmarking and hyperlinking) so important in regulatory publishing?
Answer Guidance: Bookmarks and hyperlinks allow regulatory reviewers at health agencies (like the FDA) to navigate easily through thousands of pages of clinical and CMC data, improving the review timeline and preventing submission rejection. - Q3. Explain what an XML backbone does in an electronic submission.
Answer Guidance: The XML backbone acts as a table of contents and structure map. It defines the folder hierarchy, document locations, metadata, and lifecycle status (new, replace, delete) of every file within the eCTD submission folder.
🚀 How to Apply?
Interested and eligible candidates can submit their applications directly via Piramal Pharma's official Workday careers board. Click the button below to apply:
Apply Online – Piramal Workday Career Board❓ Frequently Asked Questions
Q. What is the application deadline for this Piramal regulatory role?
The official application deadline is July 30, 2026.
Q. Can freshers apply for this Regulatory Publisher vacancy?
Yes, this position is open to candidates with 0 to 3 years of experience. Freshers with relevant science or pharmacy degrees are eligible.
Q. Is this a remote or onsite job?
This is a full-time, hybrid (onsite) position based at Piramal's office in Mumbai, Maharashtra.
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