Regulatory Affairs Opening at Hetero Healthcare
Hetero Healthcare is hiring for a Regulatory Affairs role in Hyderabad. This opportunity is suitable for candidates with a B.Pharmacy or M.Pharmacy qualification and 3 to 6 years of relevant experience in regulatory affairs activities. The role focuses on end-to-end regulatory work including dossier compilation, submissions, product registrations and regulatory compliance coordination.
Job Overview
| Company | Hetero Healthcare |
| Position | Regulatory Affairs |
| Location | Hyderabad |
| Qualification | B.Pharmacy or M.Pharmacy |
| Experience | 3 to 6 years |
| Application Mode | Email Application |
Key Responsibilities
- Handle end-to-end regulatory activities including dossier compilation.
- Work on ACTD, CTD and country-specific checklist requirements.
- Support dossier submissions for assigned markets.
- Manage product registrations and renewals.
- Coordinate variation-related regulatory activities.
- Handle regulatory query responses and artwork review.
- Ensure regulatory compliance and assess country-specific requirements.
- Coordinate with cross-functional teams and regulatory authorities for timely approvals.
Required Qualifications
- B.Pharmacy or M.Pharmacy.
Experience Required
- 3 to 6 years of experience in Regulatory Affairs.
Why This Role Is a Good Opportunity
This Regulatory Affairs opening offers candidates the opportunity to work on core regulatory activities such as CTD/ACTD dossier compilation, country-specific submissions, product registrations, renewals, regulatory compliance and cross-functional coordination. Candidates with prior experience in pharmaceutical regulatory processes can apply by sharing their updated resume through email.
How to Apply
Interested candidates can send their updated resumes to:
