💼 Trainee – Regulatory Affairs (GBS GRA PLCM)
🏢 Company: Apotex (ApoPharma)📍 Location: Mumbai, Maharashtra, India
🎓 Eligibility: B.Pharm, M.Pharm
🧪 Experience: Freshers
📝 Job Type: Full-Time | Regulatory Affairs | Office-based
🔎 Verified: ✅ Verified Job via Medical Jobs India – hitechplus.in
🏢 About Apotex
Apotex is one of the largest Canadian-owned pharmaceutical companies, delivering high-quality generic and specialty medicines worldwide. Through its affiliate ApoPharma, it is recognized for innovation, regulatory excellence, and a strong commitment to global healthcare accessibility.
📌 Key Responsibilities
- ✔ Collate, compile, and submit regulatory documentation for assigned projects.
- ✔ Coordinate tender submissions and maintain regulatory databases.
- ✔ Liaise with affiliates, customers, and health authorities regarding submissions.
- ✔ Maintain accurate regulatory records, trackers, and reports.
- ✔ Respond to internal and external regulatory queries.
✅ Eligibility & Skills
- ✅ Graduate or Postgraduate in Pharmacy (B.Pharm/M.Pharm).
- ✅ Strong academic background with an interest in regulatory affairs.
- ✅ Knowledge of new product dossier preparation and PLCM submissions (advantage).
- ✅ Theoretical understanding of regulatory affairs for International/US-CAN-EU markets.
🎁 Why Join Apotex?
- 🌐 Work with a global leader in generic and specialty pharmaceuticals.
- 📈 Gain hands-on experience in global regulatory submission processes.
- 💼 Opportunity for career growth in regulatory affairs.
- 🤝 Supportive and ethical workplace culture.
📌 Note Before You Apply:
Highlight your knowledge of dossier preparation, PLCM processes, and regulatory documentation. Showcase your academic achievements and eagerness to learn for a stronger application.
👇 Application Link Will Be Visible in 15 Seconds 👇
🟢 Verified Job via Medical Jobs India – hitechplus.in
.jpg)
.jpg)
0 Comments