to manage regulatory compliance, dossier preparation, and product registrations across
ROW markets
, including Africa, APAC, LATAM, GCC, and CIS regions.
Key Responsibilities
Ensure regulatory compliance for nutraceutical and Ayurvedic products across
ROW markets
.
Prepare, compile, and manage
CTD dossiers (Modules 1-5)
and country-specific registration documents.
Handle
lifecycle management
, variations, renewals, and responses to regulatory deficiencies.
Review manufacturing documents and convert them into compliant regulatory formats.
Prepare
SmPC, Package Inserts, labels
, and product information documents.
Provide regulatory guidance on
dosage, formulation, and preparation
.
Liaise and coordinate with
regulatory authorities
for product registrations and approvals.
Rest of world Market Exposure
Asia-Pacific | LATAM | GCC | Africa | Eastern Europe & CIS
Qualifications & Experience
2-3 years of experience in
Regulatory Affairs (ROW / Africa markets preferred)
Hands-on experience with
nutraceuticals / vitamin-based products
Strong knowledge of
CTD dossier compilation and compliance
Job Type: Full-time
Pay: ?25,000.00 - ?30,000.00 per month
Work Location: In person
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