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Vizen Life Sciences is inviting skilled Pharmacovigilance professionals to join its expanding PV operations team. This opportunity is ideal for candidates seeking growth in safety operations, EUDRA Vigilance, PSUR drafting, signal detection, quality review, and PV data management.
If you have hands-on experience in end-to-end Pharmacovigilance workflows, this hiring drive offers a strong platform to accelerate your career.
Open Positions
- EUPV
- PSUR/Signal Draft Specialist
- Peer Reviewer
- Data Entry
- Quality Reviewer
Key Responsibilities
Responsibilities will vary based on the position but may include:
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- Managing case processing activities in compliance with global PV regulations.
- Drafting and reviewing PSURs, Signal Evaluation Reports, and safety documents.
- Performing EUDRA Vigilance activities and ensuring regulatory compliance.
- Conducting quality checks for ICSRs, narratives, and safety reports.
- Managing PV data entry and documentation with high accuracy.
- Ensuring adherence to SOPs, quality metrics, and audit readiness.
Required Qualifications
- Mandatory Pharmacovigilance experience (minimum 1–5 years preferred).
- Educational background in Pharmacy, Life Sciences, Biotechnology, Nursing, or related fields.
- Strong understanding of PV regulations, MedDRA, case processing, and safety reporting.
- Excellent analytical, documentation, and communication skills.
Benefits
- Competitive industry salary
- Opportunity to work in a growing, innovation-driven PV environment
- Skill development across multi-domain PV operations
- Exposure to global Pharmacovigilance standards
How to Apply
Eligible candidates can send their updated CV to:
Email: careers@vizenlifesciences.com
Subject Line: Application for Pharmacovigilance Position – [Role Name]
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