INTERNSHIP DETAILS
Regulatory Affairs Intern
CompanyDIFGEN PHARMACEUTICALS PRIVATE LIMITED
LocationHyderabad
Work ModeOn Site
PostedJuly 8, 2026

Internship Information
Core Responsibilities
Assist in the preparation and submission of regulatory documents for product registrations and track global regulatory updates. Support the maintenance of regulatory files and collaborate with cross-functional teams to ensure compliance.
Internship Type
intern
Company Size
161
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
We are a US based Global Pharmaceutical company with a primary focus on developing complex high barrier to entry Generics and Specialty Pharmaceutical products that would help increase accessibility to high quality medication thereby leading to the creation of next generation healthy communities. We are driven by an earnest pursuit of redefining the accepted standards in pharmaceutical product development and commercialization. We consistently aspire to challenge standard thought processes to arrive at dependable solutions that create a paradigm shift in product development, quality, clinical affairs, regulatory sciences, and commercial strategy. Our talented team with some of the brightest minds have developed a holistic understanding of the nuances associated with the development of unique, commercially viable and difficult product lines across varying therapeutic areas and a broad array of dosage forms such as Injectables, Ophthalmics, Topicals, Biologicals, Drug Devices, Soft Gels, Solid Orals & Suspensions.
About the Role
Job DetailsJob Location: DifGen Pharmaceuticals Pvt Ltd- R&D - 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 DocumentationANDA SubmissionMAA SubmissionDCP SubmissionRegulatory IntelligenceLabeling ReviewPLCMMicrosoft Office SuiteCommunication SkillsOrganizational Skills
Categories
Science & ResearchHealthcareManufacturingLegal
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Week 2:Regulatory Documentation3
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