Pharmacovigilance Vacancies in Pune | PV Executive Roles Available

Adaptis Pharma,  is currently hiring Pharmacovigilance Executives. These roles are crucial for ensuring the safety and efficacy of pharmaceutical products through diligent case processing and literature monitoring.

If you hold a degree in B.Pharm or M.Pharm and have 1-2 years of experience in pharmacovigilance, this job could be a great fit for you.

Job Position: Executive – Pharmacovigilance

• Number of Positions: 02
• Location: Pune, Maharashtra (Work From Office)
• Employment Type: Full-Time
• Company: Adaptis Pharma

Adaptis Pharma is seeking skilled professionals to join their pharmacovigilance team in Pune. The role focuses on ICSR data entry and literature triage, offering an opportunity to work closely with regulatory authorities and ensure drug safety across various markets.

Key Responsibilities

As a Pharmacovigilance Executive, your role will include:

1. ICSR (Individual Case Safety Reports) Data Entry:
   • Ensuring the accuracy of adverse event reports by validating data and handling case processing.
   • Coding adverse events, medical history, and product indications using standard medical terminology (e.g., MedDRA).
2. Literature Monitoring and Triage:
   • Monitoring and downloading case reports from regulatory authorities like EMA and US FDA.
   • Screening relevant articles and ensuring proper documentation for safety reports.
3. Regulatory Compliance:
   • Drafting and summarizing narratives related to product safety.
   • Ensuring adherence to regulatory requirements for product safety and efficacy monitoring.
4. Collaboration with Stakeholders:
   • Coordinating with regulatory bodies to maintain compliance and support the product’s lifecycle.

By joining Adaptis Pharma, you will play a pivotal role in monitoring drug safety, ensuring product quality, and contributing to overall public health.

Job Qualifications

To qualify for this role, candidates must have:

• Educational Qualifications:
  • B.Pharm or M.Pharm degree.
• Experience:
  • 1-2 years of experience in pharmacovigilance, with hands-on experience in case processing and literature monitoring.
• Technical Skills:
  • Knowledge of ICSR data entry, narrative writing, and MedDRA coding.
  • Familiarity with working alongside regulatory bodies such as EMA and US FDA.
• Additional Skills:
  • Strong attention to detail and the ability to handle complex safety data.
  • Excellent communication and teamwork skills.

Location Details

This position is based in Pune, Maharashtra. The role is Work From Office (WFO)

How to Apply

Send your updated resume to info@adaptisis.com and take the next step in your career.