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 : [email protected]
EU Market : [email protected]