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Hetero Drugs is a leading pharmaceutical company based in India, known for its expertise in the development, manufacturing, and commercialization of generic medicines, biosimilars, and active pharmaceutical ingredients (APIs). Established in 1993, Hetero has a strong presence in over 126 countries, serving key therapeutic areas such as oncology, HIV/AIDS, cardiology, neurology, and more.
Regulatory Affairs Specialist
Markets: Formulation (ROW, EU ,US)
Work Location: Jeedimetla, Hyderabad
JOB DESCRIPTION:
Preparation, review and submission of Dossiers.
Good exposure on Life Cycle Management.
Handling Post approval & Pre approval.
Knowledge on MAA (Marketing Authorization Application).
Experience in CMC.
EXPERIENCE: 3 to 9 Years
QUALIFICATION: M Pharma/ B Pharma/ M Sc
How to apply ?
Candidates Interested in this role should email their CV’s to chandrasekhar.r@hetero.com
with the subject line “Application for RA”
