Are you a recent Pharmacy, Life Sciences, or Biotechnology postgraduate looking to break into the pharmaceutical regulatory sector? DDReg Pharma Pvt. Ltd. is offering an exciting 6-month full-time internship in Gurgaon for aspiring regulatory affairs professionals. Gain real-world exposure, work on global submissions, and learn from industry experts!
📌 Job Description: Regulatory Affairs Intern
As a Regulatory Affairs Intern, you will:
✔ Assist in preparing and reviewing regulatory submissions (ANDAs, DMFs, INDs, NDAs) for global markets.
✔ Gain hands-on experience with eCTD publishing tools and regulatory databases.
✔ Support in compiling, formatting, and submitting dossiers to regulatory authorities (USFDA, EMA, etc.).
✔ Work on compliance documentation and ensure adherence to ICH, GMP, and GLP guidelines.
✔ Collaborate with cross-functional teams (R&D, Quality Assurance, Clinical Research).
✔ Get mentored by industry veterans and participate in real-time regulatory projects.
🏆 Why Join DDReg Pharma?
🔹 Mentorship & Skill Development: Learn from top regulatory professionals.
🔹 Practical Exposure: Work on live regulatory submissions and compliance projects.
🔹 Certification: Receive an internship completion certificate.
🔹 Career Growth: Potential for full-time roles based on performance.
🔹 Networking: Connect with pharma industry leaders.
🎯 Eligibility Criteria
- Fresh postgraduates (M.Pharm, M.Sc, or related fields) in Pharmacy, Life Sciences, or Biotechnology.
- Basic understanding of regulatory guidelines (ICH, USFDA, EMA) is a plus.
- Strong analytical, documentation, and communication skills.
- Detail-oriented with a passion for compliance and drug regulations.
📍 Location & Duration
- 📍 Gurgaon (Onsite)
- 📅 6 Months (Full-time)
📝 How to Apply?
Send your updated resume to career@ddreg.in with the subject line:
“Application for Regulatory Affairs Internship – [Your Name]”.
🔗 Explore more opportunities at Pharmabharat.com
🔍 About DDReg Pharma Pvt. Ltd.
DDReg Pharma is a leading regulatory consulting firm specializing in global drug submissions, compliance, and lifecycle management. With expertise in USFDA, EMA, and other regulatory markets, DDReg helps pharmaceutical companies navigate complex approval processes.
