Pharmacovigilance Officer - DEMO Global Services

Demo SA; Hyderabad; On-site; INR 600,000 - 1,000,000; Full time

Benefits offered by this job

Competitive salary

Training & career development

Friendly environment

Job summary

Demo SA in Hyderabad, India is seeking a Pharmacovigilance Officer to perform PV activities across a diverse portfolio of medicinal products. You will contribute to safety signal detection, literature screening, and regulatory compliance in a fast‑growing environment.

Key responsibilities include reviewing and recording IC‑SRs in the PV database, maintaining XEVMPD data, and ensuring timely handling of safety information.

Qualifications

• Bachelor's degree in Pharmacy, Life Sciences, Biology or related field is required.
• At least 1 year hands‑on pharmacovigilance experience in pharma or PV services is preferred.
• Professional fluency in English with ability to work in an international environment.

Responsibilities

• Perform global literature screening and ICSR review per GVP requirements.
• Record and manage IC-SRs in the PV database accurately.
• Maintain XEVMPD data and ensure compliant handling of safety information.

Skills

Fluency in English

Communication skills

Cross-cultural collaboration

Digital literacy

Education

Bachelor's degree in Pharmacy/Life Sciences

Master's degree (advantage)

Tools

Pharmacovigilance databases

Job description

In this dynamic and fast growing environment, we are looking for a high caliber Pharmacovigilance Officer who will be responsible for performing pharmacovigilance activities across a diverse portfolio of medicinal products

Main duties and responsibilities:

• Perform global literature screening and review in accordance with GVP requirements.
• Review, assess, process, and accurately record Individual Case Safety Reports (ICSRs) in the company’s pharmacovigilance database.
• Conduct routine review and management of IC…
• Maintain and update the EudraVigilance eXtended Medicinal Product Dictionary (XEVMPD).
• Ensure the timely and compliant handling of safety information in line with applicable pharmacovigilance regulations and company procedures.
• Maintain accurate documentation and support pharmacovigilance activities to ensure ongoing regulatory compliance.

• Bachelor’s degree in Pharmacy, Life Sciences, Biology, or a related discipline from a recognized institution, relevant Master’s degree will be considered an advantage.
• At least one year of hands‑on pharmacovigilance experience within the pharmaceutical industry or a global PV services organisation.
• Professional fluency in English, with confidence working in an international environment.
• Strong digital literacy, including proficiency in Microsoft Office; experience with pharmacovigilance databases is an advantage.
• Excellent communication and cross-cultural collaboration skills.

The company offers competitive salary and benefits, continuous specialized training, career development and a friendly working environment.