KYDA Partners is seeking a proactive and skilled Sterile Processing Supervisor to lead the processing department. This role involves providing technical guidance, equipment support, and ensuring the highest standards of quality, safety, and compliance. The ideal candidate will identify and support growth initiatives aligned with the company's strategic business plan. M-F 4pm-midnight
Key Responsibilities:
Supervision and Scheduling: Oversee processing technicians, manage schedules, and coordinate day-to-day activities.
Operational Support: Assist the processing manager in daily operations, including personnel management, quality control, quality assurance, and proficiency testing programs.
Methodology and Protocol Development: Develop and evaluate processing methodologies, protocols, and techniques; oversee equipment care, maintenance, and inventory management.
Personnel Management: Support in recruitment, work allocation, orientation, training, staff development, performance evaluations, and employee motivation.
Validation and Compliance: Perform validations for new equipment, major repairs, processes, software updates, and modifications.
Documentation and SOPs: Create, review, and manage standard operating procedures (SOPs) and training documents. Develop, draft, revise, and review validation/verification plans, test cases, and summaries.
Issue Resolution: Provide guidance and root cause analysis for process variability and equipment reliability issues.
Liaison Role: Act as the main point of contact in the absence of the processing manager.
Administrative Duties: Attend meetings and perform various administrative tasks as required.
Education and Experience:
Educational Requirements: High school diploma required; CTBS Certification preferred.
Experience: Minimum of 2 years of experience in an FDA-regulated environment, specifically in HCT/P manufacturing.