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Sidra Medicine seeks a Senior Specialist - Research Laboratory Quality Systems to lead the design and maintenance of an integrated Quality Management System across its research cores in Qatar.
The role ensures compliance with ISO standards (9001, 17025, 15189, 20387) and CAP/GLP while coordinating with core facilities to meet stakeholder expectations. Reporting to the Executive Director of Core Facilities, you will drive risk management and continuous improvement.
Industry Quality Management and Compliance
TheSenior Specialist - Research Laboratory Quality Systems reports to the Executive Director of Core Facilities and is responsible for developing, implementing, and maintaining an integrated Quality Management System across multiple research core facilities. This role ensures compliance with ISO 9001, ISO 17025, ISO 15189, ISO 20387, CAP, GLP, ISO 19011, and ISO 31000 standards while adhering to corporate GREC requirements. Key responsibilities include developing Quality Manuals, annual reports, quarterly reviews, managing documentation, conducting internal audits, ensuring regulatory compliance, driving continuous improvement, managing risk, participating in corporate policy committees, and serving as a collaborative partner with the cores' end users to ensure harmonized quality practices and to meet stakeholder expectations across all facilities.
"Sidra Medicine a healthy population is essential to a strong, prosperous society, and throughout 2020, Sidra continued to provide uninterrupted comprehensive specialist healthcare services for children and young people; and exceptional maternity, gynecology, and reproductive medical services for women, previously unavailable in Qatar and the region."
Sidra Medicine represents the vision of Her Highness Sheikha Moza bint Nasser who serves as its Chairperson. This high-tech facility is home to world-class patient care, scientific expertise, and educational resources.