مطلوب مشرف ضمان جودة في عمان We’re Hiring QA Supervisor (IPC/Documentation) We are looking for a detail-driven quality professional with a passion for compliance and continuous improvement. Join our team as a QA Supervisor (IPC/Documentation) and play a critical role in ensuring excellence across in-process controls (IPC) and documentation practices. About the Role: As the QA Supervisor (IPC/Documentation), you will lead a team focused on monitoring and improving in-process controls and managing GMP/quality-related documentation. Your efforts will support production quality, regulatory compliance, and internal audit readiness. Key Responsibilities: • Supervise daily IPC activities to ensure compliance with SOPs, GMP, and industry standards (ISO 13485, MDR). • Lead documentation control including creation, review, issuance, and archival of controlled documents • Coordinate with cross-functional teams (Production, QC, QA, etc.) to support investigations, change control, CAPAs, and batch record reviews • Ensure data integrity and compliance with regulatory requirements (FDA, ISO 13485, MDR, etc.) • Train, mentor, and develop QA IPC/documentation team members. • Participate in audits, inspections, and continuous improvement initiatives • Training departments on cGMP, ISO 13485, MDR Standard, Safety, etc. • Review & qualification ETO related practices, equipment and calibration for tools, instruments for HVAC system, as well as, qualification for class D . Qualifications: • Bachelor’s degree in Sciences, Engineering, or any related field • 3+ years of experience in QA/IPC/documentation within a regulated industry (pharma, biotech, medical devices, etc.) • Strong understanding of GMP, FDA, and ISO standards • Excellent organizational, communication, and leadership skills [email protected] لمشاهدة جميع الوظائف الشاغرة على ثريدز اضغط شارك الوظيفة