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. Show more Show less

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.

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.