위치Mumbai, India, Andaman and Nicobar Islands, India
급여USD 15,000 - USD 25,000 /year
경력3 years – 5 years
근무 형태하이브리드
고용 형태계약직
수준중급
직무 설명
IndPharma Quality Labs is looking for a Regulatory Affairs Specialist to manage drug registration dossiers for Asian and African markets.
자격 요건
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
복리후생
Health insurance for family\n Performance bonus\n Flexible working hours\n Training & certification support
필수 역량
Regulatory AffairsAdvanced필수
Drug RegistrationAdvanced필수
Medical WritingIntermediate
어학 요건
EnglishB2필수
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마감일: 2026년 8월 1일
현재 1 명 지원
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IQ
IndPharma Quality Labs
500 - 1000 명의 직원
Premier Indian pharmaceutical manufacturing company with WHO-GMP certification. Specializing in generic formulations and API production.