Qualified Person Responsible for Pharmacovigilance (QPPV)

Company: Klybeck Life Sciences Location: Dammam, Saudi Arabia Employment Type: Full-Time | Permanent Klybeck Life Sciences is seeking a qualified pharmaceutical professional to oversee pharmacovigilance activities and support regulatory affairs for our pharmaceutical products in Dammam, Saudi Arabia Key Responsibilities • Serve as the Qualified Person Responsible for Pharmacovigilance (QPPV) for pharmaceutical products in accordance with applicable SFDA requirements. • Coordinate product registration and follow up on regulatory matters with the Saudi Food and Drug Authority (SFDA). • Oversee pharmacovigilance activities, including adverse event reporting, safety case processing, and maintaining relevant safety documentation. • Collaborate with the Regulatory Affairs team to ensure compliance with applicable regulatory requirements and timely completion of submissions and follow-up activities. Requirements • Bachelor’s degree in pharmacy. • 3–4 years of relevant experience in Pharmacovigilance. • Registration with the Saudi Commission for Health Specialties (SCFHS). • Knowledge of pharmacovigilance principles and applicable SFDA regulations. • Familiarity with adverse event reporting and regulatory documentation. Interested candidates are invited to apply by submitting their CV.