LieuMumbai, India, Andaman and Nicobar Islands, India
SalaireUSD 15 000 - USD 25 000 /year
Expérience3 years – 5 years
Type de travailHybride
Type d'emploiContrat
NiveauConfirmé
Description du poste
IndPharma Quality Labs is looking for a Regulatory Affairs Specialist to manage drug registration dossiers for Asian and African markets.
Exigences
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
Avantages
Health insurance for family\n Performance bonus\n Flexible working hours\n Training & certification support
Compétences requises
Regulatory AffairsAdvancedRequis
Drug RegistrationAdvancedRequis
Medical WritingIntermediate
Exigences linguistiques
EnglishB2Requis
Intéressé par ce poste ?
Date limite : 1 août 2026
1 candidat jusqu'à présent
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IQ
IndPharma Quality Labs
500 - 1000 employés
Premier Indian pharmaceutical manufacturing company with WHO-GMP certification. Specializing in generic formulations and API production.