Job Highlights
- Qualifications: B.Pharma, M.Pharma, or MSc in Chemistry
- Role: Assist in regulatory submissions, dossier preparation, and compliance documentation
- Skills Required: Regulatory documentation, dossier submissions, compliance tracking
Job Description
Key Responsibilities:
- Assist in the preparation and submission of regulatory documents, including dossiers for product registrations, variations, and renewals.
- Support in collecting and organizing technical data to ensure regulatory compliance.
- Help in maintaining regulatory databases and tracking the status of submissions and approvals.
- Coordinate with cross-functional teams to ensure timely regulatory filings.
- Stay updated with global regulatory guidelines (USFDA, EMA, WHO, etc.) for compliance.
Preferred Skills:
- Basic understanding of regulatory affairs in the pharmaceutical industry.
- Strong documentation and organizational skills.
- Knowledge of CTD/eCTD submissions is a plus.
- Good communication and teamwork abilities.
About Hetero
Hetero is a leading global pharmaceutical company specializing in generic drugs and active pharmaceutical ingredients (APIs). With a strong presence in over 120+ countries, Hetero is known for its high-quality, affordable medicines. The company is committed to innovation, compliance, and patient-centric healthcare solutions.
How to Apply
