INTERNSHIP DETAILS

Regulatory Affairs Intern

CompanyAVEVA DRUG DELIVERY SYSTEMS INC
LocationHyderabad
Work ModeOn Site
PostedJuly 8, 2026
Internship Information
Core Responsibilities
Assist in preparing and submitting regulatory documents for product registrations and tracking global regulatory updates. Support the maintenance of regulatory files and collaborate with cross-functional teams to ensure compliance with health authority standards.
Internship Type
intern
Company Size
247
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
AVEVA is a global leader in transdermal drug delivery located in the United States. The company has an extensive history of providing pharmaceutical partners with fully integrated, controlled-release transdermal products that fulfill unmet market needs or supply high-quality, affordable brand equivalents. By leveraging this experience, AVEVA offers a full range of research, development and manufacturing capabilities to produce transdermal pharmaceutical products that can improve the quality of life, usage and compliance rates for patients.
About the Role
Job DetailsJob Location: Prashanti Nagar IE Kukatpally Hyderabad, TELANGANA 500072Position Type: Internship Assist in the preparation and submission of regulatory documents to health authorities for product registrations, including ANDAs/MAA/DCP/ANDS etc but not limited to these. Periodic tracking of evolving Global Regulatory updates and updating to team and implimentation of the new expectations of Global competent Regulatory Agencies and review of all relevant data inclusive of the Type II DMF/ASMF etc. Support the maintenance of regulatory files and databases, PLCM, ensuring accuracy and completeness of documentation. Collaborate with cross-functional teams, including Quality Assurance, R&D, and Manufacturing, to gather necessary information for regulatory submissions. Assist in the review of labeling and promotional materials to ensure compliance with regulatory standards. Participate in regulatory intelligence activities, including monitoring regulatory updates and communicating relevant information to internal stakeholders. Provide administrative support as needed, including organizing meetings, preparing meeting agendas, and documenting meeting minutes. Any other related duties as assigned by Project Leader Master In Pharmacy Currently enrolled in  Master of Pharmacy degree program in Pharmacy, Regulatory Affairs, Life Sciences, or a related field. Strong attention to detail and organizational skills. Excellent written and verbal communication skills. Ability to work independently and collaboratively in a fast-paced environment. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). Prior experience or coursework in regulatory affairs or the pharmaceutical industry is preferred.
Key Skills
Regulatory DocumentationProduct RegistrationRegulatory IntelligenceLabeling ReviewComplianceMicrosoft Office SuiteCross-functional CollaborationData Review
Categories
HealthcareScience & ResearchManufacturingLegalAdministrative