Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India. The company manufactures generic pharmaceuticals and active pharmaceutical ingredients.
Post : Regulatory Affairs - US &EU Markets
RAD-US- ANDA Filing, RAD-US - Post Approvals(LCM), RAD-US- SPD-Topical/ Derma
Experience : 4.5 yrs to 6 yrs in RAD-US market
Qualification : B.Pharm/ M.Pharm Spec: (Regulatory Affairs/ Pharmaceutics)
RA_EU_Pre & Post Approvals , RA_EU_ CMC(LCM)
Experience
• 2 yrs to 5 yrs in EU-CMC -Post Approvals
• 8 yrs to12 yrs in EU-CMC-LCM
Qualification
• M.Pharm Spec: (Regulatory Affairs/ Pharmaceutics/Analysis, Regulatory Affairs, Quality Assurance)
Preferred candidates with hands on experience with Formulations RA in US and EU markets
Work Location : APLRC -1, Hyderabad
Interested candidates can share their Resume as below
US Market : Sreeja.Yangam@aurobincto.com
EU Market : Pooja.Uppalapati@aurobindo.com
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