Description:
Responsible for managing regulatory affairs activities and regulatory strategy execution to ensure compliance with global regulatory requirements, industry standards, and ethical practices throughout product development and lifecycle management. The role oversees preparation, review, and submission of regulatory dossiers, technical documentation, and product registration applications required for approvals from regulatory authorities. It contributes to monitoring regulatory developments, policy updates, and industry intelligence, evaluating their impact on regulatory strategies and organizational operations. The position coordinates regulatory communications, responses, and compliance documentation for interactions with health authorities. It also collaborates with cross-functional teams to strengthen regulatory governance, documentation control, and compliance monitoring, supporting timely approvals and sustainable regulatory alignment across markets.
Essential Functions:
Lead and review dossier compilation & publishing for complex submissions
Oversee DMF compilation & review process and submission strategies
Direct eCTD & electronic submissions across regions
Manage post-submission management and health authority responses
Ensure robust document version control & governance
Monitor regulatory intelligence and assess strategic impact
Drive regulatory & supplement reporting and lifecycle updates
Coordinate regulatory & health authority management engagements
Ensure inspection readiness for DMF and audit preparedness
Apply risk identification & mitigation in regulatory planning
Ensure sustained regulatory compliance across product lifecycle
Lead quality & audit readiness initiatives
Additional Responsibilities: