
Description:
- Liaise with Government departments and Regulatory Bodies including DGCA, CDSCO, International Cell, Department of Pharmaceuticals, Ministry of Health & Family Welfare, and other related agencies.
- Coordinate with Indian and foreign embassies/high commissions for issuance of letters, endorsements, and support related to drug approvals, regulatory clearances, and international registrations.
- Facilitate and follow up on drug approvals, manufacturing licenses, import/export permissions, NOCs, renewals, and statutory clearances.
- Act as the point of contact between the organization and government bodies for all regulatory and policy-related matters.
- Monitor changes in government policies, regulations, and guidelines impacting the pharmaceutical/ healthcare sector and advise management accordingly.
- Support regulatory teams in addressing queries, deficiencies, and compliance requirements raised by authorities.
- Represent the organization in meetings, hearings, and official interactions with government officials and regulatory agencies.
- Maintain strong professional relationships with key officials across departments to enable smooth and timely processing of applications.
- Prepare, vet, and submit official correspondence, representations, and compliance reports to authorities.
- Handle Plant & Cluster PR issues. Coordination with local Police, Politicians, Revenue official and Site visiting govt officers. Independently handle day to day PR and liaison activities.
- Relation building with neighbouring communities, village-heads, industries
- Extend support to the Plant management in execution of CSR and other development projects
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