Mendine Pharmaceuticals Pvt. Ltd. is a WHO-GMP and ISO 9001:2015 certified pharmaceutical company committed to delivering high-quality healthcare solutions globally. With a strong focus on innovation and compliance, Mendine Pharma offers a dynamic work environment for aspiring professionals to grow in the regulatory and quality assurance domain.
Key Responsibilities:
As a Regulatory Affairs Intern, you will gain hands-on experience in:
✔ Regulatory Documentation: Test license preparation, dossier compilation, and handling endorsement documents.
✔ Compliance Updates: Tracking regulatory notifications and ensuring adherence to guidelines.
✔ SOP Preparation: Assisting in drafting and reviewing Standard Operating Procedures (SOPs).
✔ ONDLS Portal Handling: Managing submissions and updates on regulatory portals.
✔ Cross-functional Collaboration: Working with QA, R&D, and regulatory teams.
Eligibility Criteria:
✅ Educational Qualification: M.Pharm in Regulatory Affairs (Freshers preferred).
✅ Technical Skills: Basic knowledge of MS Word, Excel, and regulatory guidelines (ICH, WHO, USFDA, etc.).
✅ Soft Skills: Strong attention to detail, analytical thinking, and good communication.
Benefits & Perks:
🔹 Hands-on Regulatory Experience: Learn from industry experts in a WHO-GMP certified company.
🔹 Career Growth: Opportunity to transition into a full-time role based on performance.
🔹 Networking: Work alongside experienced professionals in pharma compliance.
🔹 Dynamic Work Environment: Collaborative culture with real-world regulatory exposure.
How to Apply?
📩 Send your resume to: piyali.basu@mendine.com
📌 Subject Line: “Application for RA Intern – [Your Name]”
