Leeford Healthcare Limited is hiring for the position of Executive / Senior Executive – Regulatory Affairs at its Ludhiana, Punjab location. Candidates with 2–5 years of experience in pharmaceutical regulatory affairs, particularly in NPPA activities, pharmacovigilance, regulatory documentation, and drug safety coordination, can apply.
The selected candidates will handle regulatory compliance activities, coordinate adverse drug reaction (ADR) reporting, manage DCGI queries, and support regulatory submissions and documentation.
Job Details
| Particulars | Details |
|---|---|
| Company | Leeford Healthcare Limited |
| Job Role | Executive / Senior Executive – Regulatory Affairs |
| Department | Regulatory |
| Job Category | Legal & Regulatory |
| Qualification | — |
| Experience | 2–5 Years |
| Salary | ₹4–4.5 LPA |
| Job Location | Ludhiana, Punjab |
| Employment Type | Full-Time, Permanent |
| Openings | 2 |
| Industry | Pharmaceutical & Life Sciences |
Available Position
- Executive – Regulatory Affairs
- Senior Executive – Regulatory Affairs
Job Responsibilities
Candidates will be responsible for the following regulatory activities:
- NPPA and IPDMS Activities: Handle regulatory activities related to the National Pharmaceutical Pricing Authority (NPPA) and Integrated Pharmaceutical Database Management System (IPDMS).
- Pharmacovigilance Coordination: Coordinate activities related to Adverse Drug Reactions (ADRs) and other relevant drug safety information.
- ADR Case Tracking: Monitor reported case statuses, follow up on pending information, and support compliance with applicable pharmacovigilance requirements.
- Regulatory Documentation: Prepare, compile, review, and coordinate applications for Certificates of Pharmaceutical Product (COPP).
- DCGI Queries: Handle queries from the Drug Controller General of India (DCGI) and coordinate related regulatory documentation.
- Regulatory Notices: Manage regulatory queries, notices, and communications, including NSQ-related matters, received from regulatory authorities.
- FSSAI Annual Returns: Coordinate the preparation and filing of annual returns with the Food Safety and Standards Authority of India (FSSAI), wherever applicable to the company’s licensed activities.
Eligibility and Experience
- Candidates with 2–5 years of experience in pharmaceutical regulatory affairs.
- Experience in NPPA and pharmacovigilance-related activities.
- Familiarity with regulatory documentation and drug safety coordination.
Required Skills and Key Areas
- National Pharmaceutical Pricing Authority (NPPA) activities
- Integrated Pharmaceutical Database Management System (IPDMS)
- Pharmacovigilance and ADR coordination
- Drug safety case tracking and follow-ups
- Certificate of Pharmaceutical Product (COPP) applications
- DCGI queries and regulatory documentation
- Regulatory notices and NSQ communications
- FSSAI annual return preparation and filing
How to Apply for Leeford Healthcare Recruitment 2026?
Interested candidates can share their updated resumes through email or WhatsApp.
Email: talent@leeford.in
WhatsApp: 9875961129
Company Website: https://www.leeford.in/
