StandortMumbai, India, Andaman and Nicobar Islands, India
GehaltUSD 15.000 - USD 25.000 /year
Erfahrung3 years – 5 years
ArbeitsformHybrid
BeschäftigungsartVertrag
NiveauMittelstufe
Stellenbeschreibung
IndPharma Quality Labs is looking for a Regulatory Affairs Specialist to manage drug registration dossiers for Asian and African markets.
Anforderungen
B.Pharm or M.Pharm degree\n 3-5 years in regulatory affairs\n Knowledge of CTD/eCTD format\n Familiarity with WHO prequalification process\n Experience with CDSCO and international regulatory bodies
Leistungen
Health insurance for family\n Performance bonus\n Flexible working hours\n Training & certification support
Erforderliche Fähigkeiten
Regulatory AffairsAdvancedErforderlich
Drug RegistrationAdvancedErforderlich
Medical WritingIntermediate
Sprachanforderungen
EnglishB2Erforderlich
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Bewerbungsschluss: 1. August 2026
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IQ
IndPharma Quality Labs
500 - 1000 Mitarbeiter
Premier Indian pharmaceutical manufacturing company with WHO-GMP certification. Specializing in generic formulations and API production.