Looking for Pharmacovigilance Associate jobs in India? Alchemy is inviting applications from experienced pharmacovigilance professionals to join its growing Drug Safety team. This opportunity is ideal for candidates with hands-on experience in ICSR processing, MedDRA coding, WHO Drug Dictionary, safety databases, and global pharmacovigilance regulations.

If you have 1–4 years of Pharmacovigilance experience and are passionate about ensuring patient safety and regulatory compliance, this could be an excellent opportunity to advance your career in the pharmaceutical industry.

Job Overview

Key Responsibilities

As a Pharmacovigilance Associate, you will be responsible for end-to-end safety case management and regulatory compliance.

Responsibilities include:

• Perform complete Individual Case Safety Report (ICSR) processing and quality review.
• Handle case intake, data entry, medical coding, follow-up activities, and quality control.
• Create, update, and maintain safety cases in validated pharmacovigilance databases.
• Perform MedDRA coding for adverse events and WHO Drug Dictionary coding for medicinal products.
• Review narratives, seriousness, causality, listedness, coding accuracy, and submission readiness.
• Process spontaneous, literature, clinical trial, post-marketing, solicited, product complaint, medical information, and special situation cases.
• Manage follow-up requests and resolve data inconsistencies.
• Maintain inspection-ready documentation following Good Documentation Practices (GDP).
• Ensure compliance with ICH Guidelines, EU GVP, FDA, MHRA, CDSCO, SOPs, and Quality Management Systems.
• Support audits, CAPA activities, quality metrics, and process improvement initiatives.
• Collaborate with cross-functional teams to maintain high-quality pharmacovigilance operations.

Required Qualifications

Candidates should possess:

• B.Pharm
• M.Pharm
• Pharm.D
• BDS
• Other Healthcare Professional qualifications

Preferred Skills

Ideal candidates should have:

• 1–4 years of Pharmacovigilance experience.
• Hands-on experience in ICSR processing and quality review.
• Strong knowledge of MedDRA coding.
• Knowledge of WHO Drug Dictionary.
• Experience using validated pharmacovigilance safety databases.
• Understanding of global pharmacovigilance regulations.
• Strong analytical, documentation, and communication skills.
• Excellent attention to detail.
• Ability to meet regulatory timelines in a quality-driven environment.

Why Join Alchemy?

Working as a Pharmacovigilance Associate at Alchemy offers opportunities to:

• Build expertise in global Drug Safety operations.
• Work on end-to-end ICSR lifecycle management.
• Gain exposure to international pharmacovigilance regulations.
• Enhance MedDRA and WHO Drug Dictionary coding skills.
• Participate in audits, inspections, CAPA, and quality initiatives.
• Grow your career in the Life Sciences and Pharmacovigilance domain.

How to Apply

Interested candidates should send their updated resume to:

Email: ganpat@alchemytp.com

Subject Line:
Application – Pharmacovigilance Associate

Applicants are encouraged to apply as early as possible.