Pharmacovigilance Officer - DEMO Global Services

DEMO Pharmaceuticals S.A.; Hyderabad; On-site; INR 600,000 - 900,000; Full time

Job summary

DEMO Pharmaceuticals S.A. is seeking a Pharmacovigilance Officer to perform PV activities across a diverse portfolio of medicines.

You will conduct global literature screening and review, and accurately record IC SRs in the PV database. The role requires a Bachelor’s degree in Pharmacy or life sciences, at least one year of PV experience, fluent English, strong MS Office skills, and excellent communication in an international setting.

Qualifications

• Bachelor's degree in Pharmacy, Life Sciences, Biology or related field.
• At least 1 year of hands-on pharmacovigilance experience.
• Fluent in English, comfortable in international environment.
• Strong digital literacy; MS Office; PV databases advantageous.
• Excellent communication and cross-cultural collaboration skills.

Responsibilities

• Perform global literature screening and review per GVP.
• Review and record IC SRs in PV database.
• Manage IC SRs from MHRA and EMA via EudraVigilance.
• Maintain EudraVigilance XEVMPD data.
• Ensure compliant handling of safety information per PV regulations.
• Maintain documentation to support regulatory compliance.

Skills

Pharmacovigilance experience

English proficiency

Digital literacy

Communication skills

Education

Bachelor's degree in Pharmacy/Life Sciences

Master's degree advantage

Tools

Microsoft Office

PV 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 ICЅRs received from the MHRA and EMA through EudraVigilance
• 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

Requirements

• 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

Benefits

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