Review and approve quality-related procedures, specifications, test methods and records.
Oversee the approval/rejection and release of raw materials, packaging materials and finished products.
Establish, implement, maintain and continuously improve the Quality Management System (QMS) in compliance with applicable GMP, quality and feed safety requirements.
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Lead patient safety adverse event and near-miss management, including promoting incident reporting, investigating serious safety events, identifying root causes, and analysing aggregate incident data.
Develop and coordinate patient safety initiatives promoting a culture of safety, including morbidity and mortality reviews, clinical quality reviews, patient safety walkabouts, and safety committees.
Design and deliver training programmes for clinical leaders and staff, developing e-learning platforms, simulation scenarios, and workshops, and mentor junior staff.
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Assist to develop and review penalty frameworks (as required).
Assist in the conduct periodic review , design, and implement case management system and review existing investigation processes and workflows (as required)
5 years of experience in investigations, regulatory, legal and/or analysis. Experience in a supervisory/managerial role preferred.
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