💥 Indian Pharmacopoeia Commission (IPC) – Walk-In Interview 2026 🧪
🏢 Company: Indian Pharmacopoeia Commission (IPC), Ministry of Health & Family Welfare, Government of India
📍 Location: Ghaziabad, Uttar Pradesh / AIIMS Rishikesh, Uttarakhand
💼 Department: Materiovigilance Programme of India (MvPI)
🕒 Experience: 0–1 Years (preferred in Medical Device Industry/Post Market Surveillance)
🎓 Qualification:
- Graduation in Biomedical Engineering / Clinical Engineering
OR - Master’s in Pharmacy (Medical Device / Pharmacology)
OR - Master’s in Clinical Pharmacology / Regulatory Science
💰 Salary: Up to ₹32,000 per month (consolidated)
📅 Interview Date: 9 January 2026 (Friday)
⏰ Reporting Time: 9:00 AM – 10:00 AM
📍 Venue: Indian Pharmacopoeia Commission, Sector-23, Raj Nagar, Ghaziabad, Uttar Pradesh
🔹 Key Responsibilities
- Collect, collate, and analyse adverse events related to medical devices 🩺
- Plan risk identification and minimization strategies ⚠️
- Support Materiovigilance Programme activities 📊
- Perform additional duties assigned by Competent Authority ✅
- Ensure accurate reporting and database management 💻
🔹 Skills / Qualifications
- Good knowledge of computers and MS Office 💻
- Understanding of medical device adverse event reporting 🧪
- Strong analytical and documentation skills ✍️
- Ability to handle data collation and risk assessment 📈
🔹 Benefits / Perks
- Fixed monthly salary of ₹32,000 💰
- Work with a prestigious Government of India institution 🇮🇳
- Exposure to national-level public health programmes 🏥
- Opportunity to contribute to patient safety and medical device regulation 🩺
- Skill development in pharmacovigilance / materiovigilance 📚
- Stable contractual engagement with extension potential based on performance 📑
📄 Documents to Bring
- Updated resume 📄
- Educational certificates 🎓
- Experience certificates (if any) 🧾
- Aadhaar card 🆔
- Passport-size photographs 📸
- One set of self-attested photocopies 🗂
✅ Why Join IPC
- Serve under the Ministry of Health & Family Welfare in a national programme 🇮🇳
- Gain experience in regulatory science, pharmacovigilance & public health policy 🏥
- Contribute to patient safety and medical device quality across India 🩺
- Build a strong career foundation in medical device regulation and safety monitoring 🚀
❓ FAQs
Q: Age and experience requirement?
A: Not exceeding 28 years (relaxable). 0–1 years experience preferred but not mandatory.
Q: Is this a permanent government job?
A: No, one-year contractual position through an outsourcing agency, with possibility of termination or extension based on performance.
Q: Mandatory documents?
A: Original educational certificates, experience certificates (if any), Aadhaar card, updated resume, passport photos, self-attested photocopies.
Q: Will TA/DA be provided?
A: ❌ No TA/DA will be paid.
