Join our esteemed team in Tunisia as a Quality Assurance Officer, where you’ll play a pivotal role in upholding the highest standards of quality and compliance for our international clients. As a member of our Quality Team, your primary focus will be on maintaining the integrity, safety, and efficacy of pharmaceutical products.

Group 10
Responsibilities:

  • Conduct thorough assessments and synthesize Product Quality Reviews (PQR) in accordance with GMP requirements for multiple clients
  • Coordinate and facilitate effective communication of PQR synthesis across relevant stakeholders
  • Quality Control Checks
  • Compliance Monitoring to ensure compliance with regulatory requirements
  • Documentation Management
  • Provide training to manufacturing staff on quality standards, procedures, and regulations to ensure compliance
  • Quality Improvement Initiatives

Group 12
Experience:

  • Comprehensive understanding of the pharmaceutical industry, GMP principles, and associated processes (e.g., QA, QC, Validation)
  • Demonstrated experience of 2-3 years within a manufacturing site setting, showcasing proficiency in quality assurance practices
  • Exceptional attention to detail, coupled with a strong sense of rigor and the ability to effectively summarize complex information
  • Proficiency in English is essential

Quality Assurance Officer 122