Manager Compounding & Compliance, Pharmacy Administration, $5000 Bonus, FT, 9a-5:30p

Baptist Health South Florida•Coral Gables, FL

1d•Onsite

About The Position

Responsible for the creation, implementation and management of a comprehensive quality assurance program for pharmaceutical compounding within the Baptist Health South Florida System for all sterile and non-sterile preparations to ensure the highest quality standards are in place coupled with regulatory requirements. The manager will be responsible for developing a robust program that includes quality and safety management for non-sterile, sterile and hazardous compounding as well as regulatory compliance, operational optimization, education and standardized process and policies across the health system. His/her reference standards are the BHSF policies, the United States Pharmacopeia (USP), The Joint Commission accreditation standards (TJC), American Society of Health-Systems Pharmacists, the FDA, the Agency for Health Care Administration and state and federal regulations. Estimated salary range for this position is $137846.35 - $179200.26 / year depending on experience.

Requirements

Bachelors degree.
Registered Pharmacist.
Licensed Pharmacist in FL or eligible for Florida pharmacy licensure within 6 months from hire date.
Documented record of success in management of sterile compounding pharmacy operations.
Knowledgeable in Federal and State regulatory requirements governing sterile compounding.
Demonstrated ability to apply and utilize knowledge of quality management processes.
Demonstrated ability to lead and manage professionals and others through influence and collaboration across multiple sites.
Experience in Pharmacy operations, systems, technology, and personnel management.
Demonstrated ability to utilize effective communication, presentation, and analytical skills.
Demonstrated track record of self-initiative, strategic thinking, and successful planning and innovation.
Demonstrated ability to work collaboratively with health care administrators.
Minimum 5 years of experience.

Responsibilities

Creation, implementation, and management of a comprehensive quality assurance program for pharmaceutical compounding (sterile and non-sterile).
Development of a robust program including quality and safety management for non-sterile, sterile, and hazardous compounding.
Ensuring regulatory compliance, operational optimization, education, and standardized processes and policies across the health system.
Adherence to BHSF policies, USP, TJC, ASHP, FDA, AHCA, and state/federal regulations.