Qualified Person Responsible for Pharmacovigilance (QPPV)
Company: Klybeck Life Sciences Global
- Location: Dammam, Saudi Arabia
- Seniority: Entry level
- Employment type: Full-time
- Posted: 6 days ago
- Offer language: English
Job description
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.
