Great opportunity for M.Pharmacy Fresher/ Research Associate Regulatory Affairs at Aurobindo Pharma

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.

Job description:

The job listed is for a Regulatory Affairs Specialist who will be responsible for preparing and reviewing technical documents for ANDA/dossier submissions in various countries. They will need to format these documents according to CTD, ACTD, and country-specific guidelines and coordinate with other departments for any necessary technical or administrative documents. Additionally, they will be responsible for creating clear product labels and patient information leaflets, coordinating with the Drug Control Authority to obtain manufacturing licenses, and ensuring timely filing of variations and following up for approvals.

Desired Candidate Profile:

The desired candidate should be an M. Pharm fresher with good communication skills and an interest in building a career in regulatory affairs.

Educational  Qualification: M.Pharma in Any Specialization

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