Job Responsibilities:
- Review and maintain pharmaceutical product documents, specifications, and records.
- Assist with product dossiers, product registrations, and regulatory documentation.
- Coordinate with manufacturing units, quality assurance, and quality control departments.
- Review product compositions, labels, carton artwork, and package inserts.
- Ensure documentation complies with applicable pharmaceutical regulations and customer requirements.
- Maintain product-related records, certificates, and technical documents.
- Coordinate with manufacturers and customers for technical queries and document requirements.
Qualifications:
- B.Pharm or M.Pharm.
- Knowledge of pharmaceutical products, formulations, and regulatory documentation.
- Good communication and computer skills.
- Experience in pharmaceutical manufacturing, exports, or regulatory affairs will be preferred.