Pharmacy Compounding Supervisor

Torrance Memorial Medical Center•Torrance, CA
•Onsite

About The Position

Under the direction of the Assistant Director, this role serves as a Supervisor to Technicians, coordinating workflow and overseeing the effective delivery of medication for patient care. The position involves supervising both sterile and non-sterile compounding areas, developing competency assessments, and ensuring compliance with training requirements. The Supervisor will direct day-to-day aseptic preparation operations, manage cleanroom activities, and oversee the Quality Management Program related to compounding. This includes monitoring cleaning activities, temperature, and humidity, managing technology updates, and ensuring adherence to compounding SOPs. The role also involves staying informed about regulatory changes, serving as the designated person for USP 795, 797, and 800, and overseeing investigational drug studies.

Requirements

  • Bachelors Pharmacy Degree Program
  • 3 years of experience in Sterile Compounding
  • Pharmacist's License

Responsibilities

  • Supervise the workflow in sterile and non-sterile compounding areas, including training and tracking compliance of employees.
  • Develop competency assessments and ensure compliance with training requirements.
  • Direct day-to-day aseptic preparation operations in cleanrooms, ensuring safe, efficient, and timely delivery of sterile compounds.
  • Assume responsibility for all activities within the cleanroom during preparation sessions, adhering to Standard Operating Procedures (SOP).
  • Monitor cleanroom workflow and assign staff duties accordingly.
  • Oversees the Quality Management Program related to compounding, including surface sampling, microbial growth trends, and hood certifications.
  • Track and analyze cleaning activities, temperature, and humidity monitoring in clean areas.
  • Manage technology updates and changes in workflow systems.
  • Ensure adherence to compounding SOPs and review/update policies as necessary.
  • Stay informed about regulatory changes and implement necessary updates.
  • Serve as the designated person for USP 795, 797 and 800.
  • Oversee investigational drug studies.
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