地点Mumbai, India, Andaman and Nicobar Islands, India
薪资USD 15,000 - USD 25,000 /year
经验3 years – 5 years
工作类型混合办公
就业类型合同制
级别中级
职位描述
IndPharma Quality Labs is looking for a Regulatory Affairs Specialist to manage drug registration dossiers for Asian and African markets.
要求
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
Health insurance for family\n Performance bonus\n Flexible working hours\n Training & certification support
所需技能
Regulatory AffairsAdvanced必需
Drug RegistrationAdvanced必需
Medical WritingIntermediate
语言要求
EnglishB2必需
对这份工作感兴趣?
截止日期: 2026年8月1日
已有 1 人申请
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IQ
IndPharma Quality Labs
500 - 1000 名员工
Premier Indian pharmaceutical manufacturing company with WHO-GMP certification. Specializing in generic formulations and API production.