Pharmacovigilance Specialist

We are looking for a Pharmacovigilance Specialist to support key pharmacovigilance (PV) activities, focusing on the oversight, coordination, and quality assurance of safety processes and documentation. The role directly supports the Pharmacovigilance Manager and requires strong project coordination and compliance skills across core PV deliverables.

Key Responsibilities

• Coordinate and oversee the preparation, review, and submission of Risk Management Plans (RMPs), Periodic Safety Update Reports (PSURs), and Safety Risk Assessments.
• Support the implementation and maintenance of additional risk minimisation measures (aRMMs).
• Contribute to quality and compliance through local SOP development aligned with global standards, PV training delivery, PSMF updates, and vendor oversight.
• Manage pharmacovigilance agreements (PVAs) and safety data exchange agreements (SDEAs), ensuring timely creation, review, and maintenance.
• Participate in internal audits and compliance reviews to support continuous PV system improvement.

Candidate Profile

• Education: Master’s Degree in Life Sciences, Health, or Biomedical Sciences.
• Experience: 4–5 years of proven experience in Pharmacovigilance.
• Skills:
  • Solid understanding of PV regulations, quality systems, and safety deliverables.
  • Excellent communication skills with the ability to manage cross-functional collaboration.
  • Strong organisational and documentation abilities.
• Applicant must be in possession of a valid work permit. 

Benefits

• Competitive remuneration package;
• Comprehensive health insurance;
• Hybrid working arrangements;
• Safe and conducive working environment;
• On-the-job training and professional development in a state-of-the-art facility equipped with the latest technologies.