IndPharma Quality Labs is looking for a Regulatory Affairs Specialist to manage drug registration dossiers for Asian and African markets.
Requirements
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
Benefits
Health insurance for family\n Performance bonus\n Flexible working hours\n Training & certification support
Required Skills
Regulatory AffairsAdvancedRequired
Drug RegistrationAdvancedRequired
Medical WritingIntermediate
Language Requirements
EnglishB2Required
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Deadline: August 1, 2026
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IQ
IndPharma Quality Labs
500 - 1000 employees
Premier Indian pharmaceutical manufacturing company with WHO-GMP certification. Specializing in generic formulations and API production.