The Sterile Compounding Quality Manager will assist in supporting and maintaining cleanroom quality standards and sterile compounding processes to meet or exceed regulatory, accreditation, and quality requirements for all cleanrooms nationally. Serves as the primary quality resource for an assigned operating area, providing support to other areas as needed including after-hours and weekend support during urgent quality events. Responsible for monitoring, trending, and analyzing quality metrics, identifying risks, and implementing corrective and preventive actions. Evaluates and recommends process improvements to enhance the quality, consistency, compliance, and safety of compounded sterile preparations (CSPs). Collaborates with appropriate stakeholders to ensure organization adherence to current regulations, industry standards, and best practices for sterile compounding. Ability to independently with a high degree of autonomy, demonstrating sound judgement, initiative, and the ability to effectively manage multiple priorities while partnering with leadership and Cleanroom Help team to achieve quality, clinical and regulatory goals.
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Job Type
Full-time
Career Level
Senior
Education Level
No Education Listed