Senior Pharmacovigilance Specialist

• Support global and local PV systems and ensure compliance with international or local regulations
• Take on additional regional or local PV responsible person roles for simple PV systems
• Act as Project Manager or deputy Project Manager for assigned projects
• Perform accurate forecasting and contribute to budget planning for efficient functioning of the QPPV Office
• Update SOPs and act as a subject matter expert for PV in assigned company processes
• Maintain KPI reports and perform core and standard PV activities for assigned contractual partners
• Manage full or local Pharmacovigilance systems and projects, central pharmacovigilance activities, end-to-end case processing, Aggregate Safety Reports, Risk Management Plans, and risk minimization activities
• Act as customer contact point, ensuring consistent communication and escalation management across assigned projects
• Act as appointed EU QPPV or deputy EU QPPV, if applicable
• Ensure high-quality PV service performance in the assigned region/country and timely communication with Health Authorities
• Ensure inspection/audit readiness and finding remediation

• Biologist, Pharmacist, Medical Doctor, or other life science degree
• 4-year experience in global Pharmacovigilance activities
• Fluent English
• Computer literacy (MS Office), experience with PV databases (Veeva Vault Safety experience is an advantage)
• Strong organizational and time management skills
• Ability to work independently and in a team
• Strong organization, prioritization, and time management with reliable delivery of commitments
• Strong communication and relationship building skills across functional teams

• Professional growth and career opportunities
• International team and environment
• Bonus based on annual performance
• Personal accident and business trip insurance
• Additional health insurance
• Remote/home based
• Rewarding referral policy
• Workplace establishment allowance (fully remote)
• Team building, global meetings, B active events