勤務地Mumbai, India, Andaman and Nicobar Islands, India
給与USD 15,000 - USD 25,000 /year
経験3 years – 5 years
勤務形態ハイブリッド
雇用形態契約
レベル中堅
職務内容
IndPharma Quality Labs is looking for a Regulatory Affairs Specialist to manage drug registration dossiers for Asian and African markets.
応募要件
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
福利厚生
Health insurance for family\n Performance bonus\n Flexible working hours\n Training & certification support
必須スキル
Regulatory AffairsAdvanced必須
Drug RegistrationAdvanced必須
Medical WritingIntermediate
語学要件
EnglishB2必須
この求人に興味がありますか?
応募締切: 2026年8月1日
現在 1 人が応募中
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IQ
IndPharma Quality Labs
500 - 1000 人の従業員
Premier Indian pharmaceutical manufacturing company with WHO-GMP certification. Specializing in generic formulations and API production.