Pharmacovigilance Job at MS Pharma in Saudi Arabia
Searching for a Pharmacovigilance Officer job in Riyadh in the pharmaceutical industry? MS Pharma is hiring a Pharmacovigilance Officer to manage drug safety and compliance activities. This Pharmacovigilance Job in Saudi Arabia focuses on maintaining pharmacovigilance systems and ensuring regulatory compliance. Candidates will handle safety reporting, audits, and communication with health authorities. It is an excellent opportunity for pharmacy or medical graduates interested in drug safety. Apply now to build a career in pharmacovigilance and regulatory affairs.
About MS Pharma:
MS Pharma is a leading pharmaceutical company focused on delivering high-quality and affordable medicines across the Middle East and beyond. The company is committed to maintaining strict regulatory standards and ensuring patient safety through robust pharmacovigilance systems. With a strong presence in Saudi Arabia and other regions, MS Pharma emphasizes innovation, compliance, and continuous improvement in drug safety and healthcare solutions.
Job Details:
- Job Role: Pharmacovigilance Officer
- Location: Riyadh, Riyadh, Saudi Arabia
- Employment Type: Full-time
- Eligibility: Saudi Nationals only (as per government regulations)
- Experience Required: 1–2 years
Key Responsibilities:
Executive & Technical Duties:
- Maintain pharmacovigilance system compliance with internal and external requirements
- Act as a Qualified Person for Pharmacovigilance (QPPV) as assigned
- Serve as primary contact for regulatory and health authorities
- Monitor changes in local PV regulations and safety concerns
- Communicate updates with global PV and regulatory teams
Safety Case Processing & Reporting:
- Process and submit safety case reports to local authorities
- Prepare and review PV documents such as periodic safety reports and risk management plans
- Perform pharmacovigilance labeling and packaging review
System & Documentation Management:
- Manage the Pharmacovigilance System Master File (PSMF) and the national PSSF
- Maintain documentation, archiving, and compliance records
- Conduct literature screening and safety data monitoring
Audits & Compliance:
- Support audits and inspections, and complete CAPAs
- Ensure adherence to PV regulations and company procedures
- Maintain up-to-date regulatory intelligence
Collaboration & Communication:
- Liaise with healthcare professionals for safety information
- Support global PV teams in regulatory responses and translations
- Participate in training and act as Subject Matter Expert for PV agreements
Additional Responsibilities:
- Perform monthly reconciliation with HQ
- Handle additional tasks as directed by management
Educational Requirements for this Job:
- Bachelor’s degree in Medicine
- Basic training in epidemiology and biostatistics
- 1–2 years of experience in Medical Affairs, Marketing, or Sales in pharma
Skills Required:
- Basic understanding of pharmacology and drug safety concepts
- Knowledge of pharmaceutical industry regulations
- Familiarity with medical terminology and documentation
- Strong attention to detail and organizational skills
- Ability to work under pressure and manage confidential data
- Good communication skills in English and Arabic
- Critical thinking and problem-solving abilities
- Proficiency in MS Office applications
- Teamwork and willingness to learn
Benefits of the Pharmacovigilance Job:
- Opportunity to work in the pharmacovigilance and drug safety domain
- Exposure to regulatory compliance and global PV systems
- Career growth in the pharmaceutical and regulatory fields
- Hands-on experience with audits, inspections, and safety reporting
- Work with a reputed pharmaceutical organization in the Middle East
