Indian Pharmacopoeia Commission – Jr Materiovigilance Associate Vacancies

Jr Materiovigilance Associate – M.Pharm/Biomedical – Ghaziabad (4 Posts)

Indian Pharmacopoeia Commission hiring 4 Jr Materiovigilance Associates in Ghaziabad. M.Pharm, Biomedical eligible. Salary ₹32,000. Walk-in 9 Jan 2026.

The Indian Pharmacopoeia Commission (IPC), functioning under the Ministry of Health & Family Welfare, Government of India, has announced a walk-in interview for the position of Junior Materiovigilance Associate under the Materiovigilance Programme of India (MvPI). This hiring drive is aimed at strengthening India’s national medical device safety monitoring framework and is an excellent opportunity for pharmacy, biomedical, and clinical engineering graduates looking to build a career in regulatory affairs, medical device vigilance, and post-market surveillance. The engagement will be on a contractual basis through an authorized manpower agency, offering direct exposure to national-level pharmacovigilance and materiovigilance systems.

Company Overview

The Indian Pharmacopoeia Commission is an autonomous institution under the Ministry of Health & Family Welfare, Government of India. IPC plays a critical role in setting standards for drugs, medical devices, and healthcare products in India. It acts as the National Coordination Centre for both the Pharmacovigilance Programme of India (PvPI) and the Materiovigilance Programme of India (MvPI), ensuring patient safety through systematic monitoring of adverse events related to medicines and medical devices. Working with IPC provides unmatched credibility, regulatory exposure, and hands-on experience in public health safety systems, making it a high-value career opportunity for life sciences professionals.

Job Role & Responsibilities

As a Junior Materiovigilance Associate, the selected candidate will be directly involved in monitoring, evaluating, and managing adverse events associated with medical devices. This role is central to improving patient safety and regulatory compliance across India’s healthcare system.

Key Responsibilities

• Collection, collation, and analysis of adverse events related to medical devices
• Handling post-market surveillance data for medical devices
• Assisting in risk identification, risk assessment, and risk minimization activities
• Supporting quality assurance and regulatory documentation
• Coordinating with healthcare professionals and reporting centers
• Maintaining databases and reports using computer-based systems
• Performing any additional duties assigned by the Competent Authority

This role offers practical exposure to high CPC domains such as medical device regulatory affairs, pharmacovigilance jobs, materiovigilance careers, and healthcare compliance roles.

Eligibility / Qualifications

Candidates must meet the following educational and professional requirements to be considered for the walk-in interview.

Educational Qualification

Graduation or postgraduation in any of the following disciplines: Biomedical Engineering, Clinical Engineering, M.Pharm (Medical Devices), M.Pharm (Pharmacology), M.Pharm (Regulatory Affairs), M.Pharm (Clinical Pharmacy), Master’s in Clinical Pharmacology, Master’s in Regulatory Science

Experience

• Minimum 0 to 1 year of experience
• Experience or exposure in Medical Device Industry, Post Market Surveillance, Medical Devices, Quality Assurance, Regulatory Affairs, or Quality Management Systems will be preferred

Age Limit

• Not exceeding 28 years (age relaxation may be considered at the discretion of the Competent Authority)

Additional Skills

• Good working knowledge of computers
• Ability to handle regulatory and safety-related documentation
• Strong analytical and reporting skills

Location & Salary

Place of Posting

• Indian Pharmacopoeia Commission, Ghaziabad
• AIIMS, Rishikesh

Salary Structure

• Consolidated monthly remuneration: ₹32,000

This salary level is competitive for entry-level pharmacovigilance and medical device safety jobs in the government and healthcare regulatory sector.

Walk-in Interview Details

• Interview Date: 9 January 2026
• Reporting Time: Between 9:00 AM to 10:00 AM (Latecomers will not be entertained)
• Interview Venue: Indian Pharmacopoeia Commission, Sector-23, Raj Nagar, Ghaziabad, Uttar Pradesh

No TA/DA will be paid for attending the interview.

Required Documents for Interview

Candidates must carry originals along with one set of self-attested photocopies of the following documents:

• Educational qualification certificates
• Final year marksheet or degree certificate
• Experience certificates (if applicable)
• Updated resume
• One passport-size photograph
• Aadhaar Card (original)

Candidates without final qualification proof will not be allowed to appear for the interview.

Contract Period & Conditions

• The engagement will be purely contractual for a period of one year
• Performance and conduct will be reviewed during the tenure
• Services may be terminated at any time if performance is found unsatisfactory

Application Process

This recruitment is strictly through walk-in interview. Interested and eligible candidates must report to the interview venue on the scheduled date with all required documents. Selection updates will be communicated only through the IPC-authorized manpower agency. No individual queries regarding selection or rejection will be entertained.

FAQs

Who can apply for Jr Materiovigilance Associate at IPC?

Candidates with Biomedical Engineering, Clinical Engineering, M.Pharm, Clinical Pharmacology, or Regulatory Science qualifications can apply.

Is this a permanent government job?

No. This is a contractual position for one year through an authorized manpower agency.

Is prior experience mandatory?

No. Freshers with 0–1 year of experience are eligible.

What is the salary for Jr Materiovigilance Associate?

The consolidated salary is ₹32,000 per month.

Where is the interview conducted?

The walk-in interview will be conducted at Indian Pharmacopoeia Commission, Ghaziabad.

Company	Indian Pharmacopoeia Commission (IPC)
Vacancies	4 Posts
Required Education	Biomedical Engineering, Clinical Engineering, M.Pharm (Medical Devices, Pharmacology, Regulatory Affairs, Clinical Pharmacy), MSc Clinical Pharmacology, Regulatory Science
Experience	0–1 Years