Regulatory Affairs Intern Jobs in Medifodil Smart Pharma Solutions, KPHB - Hyderabad, Telangana

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Regulatory Affairs Intern Jobs in Medifodil Smart Pharma Solutions, KPHB - Hyderabad, Telangana

work outline icon0 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Medifodil Smart Pharma Solutions, KPHB, Hyderabad

time outline iconHyderabad, Telangana, India

Posted on 28-01-2026

1 Vacancy

Description

  1. Job Title: Regulatory Affairs Intern
  2. Qualification: BPharm/MPharm
  3. Location: Medifodil Smart Pharma Solutions, KPHB - Hyderabad, Telangana
  4. Work Experience: 0 to 5 Years

Job Description

  1. Assist in preparation and review of regulatory documents.
  2. Support compilation of dossiers (CTD / eCTD).
  3. Help maintain regulatory databases and document trackers.
  4. Perform guideline and regulatory requirement research.
  5. Support submissions to regulatory authorities.
  6. Assist in responding to regulatory queries.
  7. Maintain proper documentation and version control.
  8. Coordinate with QA, R&D, and regulatory teams.
  9. Ensure compliance with internal SOPs and timelines.

Take this opportunity to join Medifodil Smart Pharma Solutions, KPHB - Hyderabad, Telangana as a Regulatory Affairs Intern in Hyderabad, Telangana and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.

Category

Pharmaceuticals

Preferred Education

MPharm (Master Of Pharmacy)BPharm (Bachelor Of Pharmacy)

Key Skills

DocumentationVerbal Communication SkillsTime Management SkillsTeamwork

About Organization

Medifodil Smart Pharma Solutions, KPHB, Hyderabad, Telangana, is a progressive pharmaceutical and healthcare solutions company focused on quality, compliance, and innovation. The company is expanding its regulatory team and inviting applications for this role. The responsibilities include assisting with regulatory submissions and documentation, supporting compliance activities with local and global regulatory guidelines, coordinating with cross-functional teams, preparing regulatory reports, and maintaining regulatory records. This opportunity offers valuable exposure to regulatory affairs, professional skill development, and long-term career growth in a structured and supportive pharmaceutical environment.

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