Quality Assurance Specialist 230

Quality Assurance Specialist 230

004-placeholder Tunis, Tunisia - Onsite and offsite both - Life Cycle - Quality & compliance - 003-clock Permanent contract *
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 5+ 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 Specialist 230

Privacy Preference Center

Manage Consent Preferences

Always Active