Demo S.A.
Pharmacovigilance Officer - DEMO Global Services
India
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- Seniority
- Mid level
- Country
- IN
- Work mode
- On-site / unstated
- First seen by hirly
- 25 Sept 2026
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the posting
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 ICSRs 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.
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