MPharm Job at Cadila Pharmaceuticals | Apply Now for the Assistant General Manager Role
Looking to build a strong career in Regulatory Affairs? This MPharm Job focuses on registration dossier submissions, renewals, and coordination for multiple African countries. As a Regulatory Affairs Specialist, you will support product approvals, manage lifecycle updates, and collaborate closely with cross-functional teams to ensure regulatory compliance across Region I markets.
- Job Post: Assistant General Manager
- Location: Ahmedabad
About the Company
Cadila Pharmaceuticals Limited is one of India’s largest privately held pharmaceutical companies, headquartered in Ahmedabad, Gujarat, with a legacy stretching back to 1951. Founded by Shri I.A. Modi, Cadila has built a reputation for innovation-driven drug discovery, developing affordable and quality medicines for diverse therapeutic areas including cardiovascular, gastrointestinal, anti-infectives, and oncology. The company’s robust research, global manufacturing footprint, and commitment to healthcare affordability have enabled it to serve patients in over 100 countries, while its pioneering products and community health initiatives such as the Kaka-Ba Hospital showcase its dedication to improving lives and advancing medical progress.
Pharma Job Responsibilities
- To ensure Registration dossier submission of products in different Africa countries (Region I) as per agreed timeline.
- To ensure Renewal of registered product prior to validity expiration of Africa countries (Region I).
- To Review Registration and Re-registration dossiers before submission in all Africa countries (Region I).
- To maintain country-wise registered product status for all Africa countries (Region I).
- To co-ordinate with other departments R&D, QA and QC for ensuring the filings & query responses.
- To provide technical support to team for preparation of Registration/Re-registration dossiers and query responses.
- To prepare documents for variation filings as and when required for all Africa countries (Region I).
- To update registration information in SAP & Cadinet for Africa countries (Region I).
- To clear issues of commercial Order related to regulatory department for Africa countries (Region I).
- To review the tender requirements and extend necessary support by providing the required documents and samples.
- To co-ordinate with International country managers for smooth scheduling the registration activity.
Qualifications of the Pharma Job
M. Pharma.
