Hetero, a globally renowned pharmaceutical company, has announced an exciting career opportunity for professionals in the field of regulatory affairs. The company is actively seeking experienced candidates for the position of Regulatory Affairs Specialist at its Jeedimetla, Hyderabad location.
About the Role
This role is focused on the Formulation Market across ROW (Rest of the World), EU, and US regions. The Regulatory Affairs Specialist will play a key role in ensuring compliance with international regulatory standards and will be instrumental in supporting product approvals and life cycle management.
Key Responsibilities
Preparation, review, and submission of dossiers.
Exposure to Life Cycle Management.
Handling both Post-approval and Pre-approval processes.
In-depth understanding of Marketing Authorization Applications (MAA).
Experience in CMC (Chemistry, Manufacturing, and Controls).
Candidate Profile
Experience: 3 to 9 years
Qualification: M. Pharma / B. Pharma / M. Sc
This position offers an excellent opportunity to work in a dynamic, growth-oriented environment and contribute to the development and regulatory success of pharmaceutical products on a global scale.
How to Apply
Interested candidates are encouraged to send their updated CVs to chandrasekhar.r@hetero.com
with the subject line:
“Application for RA”
Join Hetero – Be a Part of Something Bigger!
With its commitment to innovation and excellence, Hetero continues to be a leader in the pharmaceutical industry. Don’t miss your chance to be part of a team that’s transforming healthcare globally.
