Safety & PV Specialist

Roles & Responsibilities
• Process adverse event reports from all sources with complete data entry and medical review
• Assess seriousness, expectedness, causality, and outcome of reported adverse events
• Ensure accurate suspect drug selection within the Pharmacovigilance Safety System (PSS)
• Prepare clear and comprehensive medical narratives for safety cases
• Code medical terms using standardized dictionaries such as MedDRA
• Initiate case investigations and perform follow-ups with reporters and local affiliates
• Conduct quality checks and case clean-up activities to support aggregate reporting
• Ensure compliance with global and regional pharmacovigilance regulations
• Meet timelines while managing multiple cases and changing priorities

Qualification
• Degree in Nursing, Pharmacy, Life Sciences, or equivalent

Experience
• 2–3 years of experience in hospital patient care or pharmaceutical industry preferred
• Prior exposure to pharmacovigilance case processing is an advantage

Skills
• Strong knowledge of adverse event reporting and drug safety processes
• Proficiency in Pharmacovigilance Safety Systems
• Excellent written and verbal communication skills
• Strong attention to detail and quality focus
• Ability to work independently under tight deadlines
• Good multitasking and time management skills
• Team-oriented and adaptable working style

About the Organization
Baxter is a global healthcare leader dedicated to saving and sustaining lives, with a strong presence in medical products, digital health, and pharmaceutical safety, offering employees meaningful work, global exposure, and long-term career growth opportunities.