Hetero is one of India’s leading generic pharmaceutical companies and the world’s largest producer of anti-retroviral drugs. Backed by 25 years of expertise in the pharmaceutical industry, Hetero’s strategic business areas spread across APIs, generics, biosimilars, custom pharmaceutical services and branded generics. The company is globally recognized for its strengths in Research and Development, manufacturing and commercialization of a wide range of products.
Hetero has 36 state-of-the-art manufacturing facilities strategically located worldwide, approved by stringent global regulatory authorities. Our portfolio includes 300 plus products encompassing major therapeutic categories such as HIV/AIDS, Oncology, Cardiovascular, Neurology, Hepatitis, Nephrology, Urology, Diabetes, Ophthalmology, Hepatology and Immunology etc.
Job Description
Desired Candidate Profile
1. 1 to 7 years of Work Experience.
2. Qualification B. Pharmacy / M. Pharmacy.
Experience: 1 to 6 year(s)
Location: Hyderabad/Secunderabad
Openings: 15
Roles and Responsibilities:
Pre-approval:
1. Review of quality documents as per regulatory requirements.
2. Compilation of dossier sections as per CTD format and submission of regulatory authorities.
3. Response with respective to agencies quarries.
Post-approvals:
1.Preparation and submission of variations for different changes as per Regulatory guidelines.
2. Response to comments with receptive to raise on submitted variations to the agencies.
Good Knowledge on ANDA, ROW, EU, US, CIS Markets
Date and Venue
29th October, 9.30 AM – 3.00 PM
Venue: Hetero Labs Limited, Unit VII, Plot:No;14, Sy.No:50,Jeedimetla,Qutubullapur(M), Medchal Dist., Hyderabad. T.S. (view on Map)
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