Sterile Processing Manager

2 months ago


San Antonio, Texas, United States KYDA Partners Ltd Full time

KYDA Partners Ltd is seeking a highly skilled and experienced Sterile Processing Manager to lead the processing department. This role involves providing technical guidance, equipment support, and ensuring the highest standards of quality, safety, and compliance.

**Key Responsibilities:**

  • Department Leadership: Oversee processing technicians, manage schedules, and coordinate day-to-day activities to ensure efficient and effective processing operations.
  • Operational Support: Assist the processing manager in daily operations, including personnel management, quality control, quality assurance, and proficiency testing programs to maintain regulatory compliance.
  • Methodology and Protocol Development: Develop and evaluate processing methodologies, protocols, and techniques to ensure optimal equipment care, maintenance, and inventory management.
  • Personnel Management: Support in recruitment, work allocation, orientation, training, staff development, performance evaluations, and employee motivation to foster a positive and productive work environment.
  • Validation and Compliance: Perform validations for new equipment, major repairs, processes, software updates, and modifications to ensure regulatory compliance and maintain a high level of quality.
  • Documentation and SOPs: Create, review, and manage standard operating procedures (SOPs) and training documents to ensure clarity and consistency in processing operations.
  • Issue Resolution: Provide guidance and root cause analysis for process variability and equipment reliability issues to minimize downtime and optimize processing efficiency.
  • Liaison Role: Act as the main point of contact in the absence of the processing manager to ensure seamless communication and coordination.
  • Administrative Duties: Attend meetings and perform various administrative tasks as required to support the processing department.

**Requirements:**

  • Education: High school diploma required; CTBS Certification preferred.
  • Experience: Minimum of 2 years of experience in an FDA-regulated environment, specifically in HCT/P manufacturing.


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