The Program Manager manages all operations related to Compounded Sterile Product (CSP) and Non-Sterile Products and Hazardous Drugs (HD) at the VA Sierra Nevada Health Care System following USP , and USP Standards. This includes compliance oversight of all pharmacists, technicians, trainees, and other supportive personnel involved in sterile and non-sterile compounding, cleaning, and disinfecting clean room areas, and/or hazardous drug management. Applicants pending the completion of educational or certification/licensure requirements may be referred and tentatively selected but may not be hired until all requirements are met. Basic Requirements: U.S. citizenship. Non-citizens may be appointed when it is not possible to recruit qualified citizens in accordance with VA Policy. English Language Proficiency. Pharmacists must be proficient in spoken and written English as required by 38 U.S.C. 7402(d) and 7407(d).Education. Graduate of an Accreditation Council for Pharmacy Education (ACPE) accredited College or School of Pharmacy with a baccalaureate degree in pharmacy (BS Pharmacy) and/or a Doctor of Pharmacy (Pharm.D.) degree. (NOTE: Prior to 2005 ACPE accredited both baccalaureate and Doctor of Pharmacy terminal degree program. Today the sole degree is Doctor of Pharmacy). TRANSCRIPTS MUST BE SUBMITTED WITH APPLICATION Graduates of foreign pharmacy degree programs meet the educational requirement if the graduate is able to provide proof of achieving the Foreign Pharmacy Graduate Examination Commission (FPGEC) Certification, which includes passing the Foreign Pharmacy Graduate Equivalency Examination (FPGEE) and the Test of English as a Foreign Language Internet-Based Test (TOEFL iBT). YOU MUST SUBMIT A COPY OF FPGEE AND TOEFL WITH YOUR APPLICATION NOTE: Prior to 2005 ACPE accredited both baccalaureate and Doctor of Pharmacy terminal degree program. Today the sole degree is Doctor of Pharmacy.)Graduates of foreign pharmacy degree programs meet the educational requirement if the graduate is able to provide proof of achieving the Foreign Pharmacy Graduate Examination Commission (FPGEC) Certification, which includes passing the Foreign Pharmacy Graduate Equivalency Examination (FPGEE) and the Test of English as a Foreign Language Internet-Based Test (TOEFL iBT). Licensure. Full, current and unrestricted license to practice pharmacy in a State, Territory, Commonwealth of the United States (i.e., Puerto Rico), or the District of Columbia. The pharmacist must maintain current registration if this is a requirement for maintaining full, current, and unrestricted licensure. A pharmacist who has, or has ever had, any license(s) revoked, suspended, denied, restricted, limited, or issued/placed in a probationary status may be appointed only in accordance with the provisions in VA Handbook 5005, Part II, Chapter 3, section B, paragraph 16. YOU MUST SUBMIT A COPY OF CURRENT LICENSE WITH THE APPLICATION PACKAGE May qualify based on being covered by the Grandfathering Provision as described in the VA Qualification Standard for this occupation (only applicable to current VHA employees who are in this occupation and meet the criteria). All licensed pharmacists employed in VHA in this occupation on the effective date of this qualification standard are considered to have met all qualification requirements for the title, series and grade held, including positive education and licensure/certification/registration that are part of the basic requirements of the occupation. For employees who do not meet all the basic requirements required in this standard, but who met the qualifications applicable to the position at the time they were appointed to it, the following provisions apply: Employees grandfathered into the GS-660 occupational series may be reassigned, promoted up to and including the full performance (journey) level, or changed to lower grade within the occupation, but may not be promoted beyond the journey level or placed in supervisory or managerial positions. Employees who are appointed on a temporary basis prior to the effective date of the qualification standard may not have their temporary appointment extended or be reappointed, on a temporary or permanent basis, until they fully meet the basic requirements of the standard. Employees initially grandfathered into this occupation, who subsequently obtain additional education and/or licensure/certification/registration, that meet all the basic requirements of this qualification standard must maintain the required credentials as a condition of employment in the occupation. Grade Determinations: In addition to the basic requirements for employment stated above, the following criteria must be met when determining the grade of candidates. Creditable Experience. Knowledge of Professional Pharmacy Practices. To be creditable, the experience must have demonstrated the use of knowledge, skills, and abilities associated with professional pharmacy practice. Professional practice means paid/non-paid employment as a professional or unlicensed graduate pharmacist as defined by the appropriate licensing board. Quality of Experience. Qualifying experience must be at a level comparable to pharmacy experience at the next lower level. Experience as a Graduate Pharmacist is creditable provided the candidate was used as a professional pharmacist (under supervision) and subsequently passed the appropriate licensure examination. Part-time Experience. Part-time experience as a professional pharmacist is credited according to its relationship to the full-time workweek. For example, a pharmacist employed 20 hours a week, or on a 1/2-time basis, would receive 1 full-time workweek of credit for each 2 weeks of service. Clinical Pharmacist Specialist, GS-13 Experience. One year of experience equivalent to the next lower grade level GS12. Knowledge, Skills, and Abilities( KSAs). The WH CPS provider must demonstrate the following knowledge, skills, and abilities to complete the duties of the position, including the necessary skills to provide care appropriate to the population of the patients served: a. Ability to communicate orally and in writing to persuade and influence clinical and management decisions b. Expert understanding of regulatory and quality standards for their program area c. Ability to solve problems, coordinate and organize responsibilities to maximize outcomes in their program area or area of clinical expertise d. Expert knowledge of a specialized area of clinical pharmacy practice or specialty area of pharmacy e. Advanced skill in monitoring and assessing the outcome of drug therapies, including interpretation of laboratory and other diagnostic parameters Candidates for the WH CPS provider should possess the skills outlined above with specific experience in the practice area of primary care. Candidates should have recent experience in a current or previous job (including residency training) that includes direct patient care and CMM responsibilities. Preferred candidates will have an advanced pharmacy degree (Pharm.D.), board certification (BPS), PGY1 Pharmacy Practice Residency, or equivalent experience or mentorship, experience in telehealth modalities of care (e.g., Clinical Video Telehealth, VA Video Connect) Preferred Experience: PGY1 residency, significant experience in PACT and/or Women's Health References: VA Handbook 5005, Part II, Appendix G15, dated June 7, 2012, VA Pharmacist Qualification Standards, GS-660.The full performance level of this position is GS-13 Physical Requirements: There may be some walking, standing, sitting, bending, and carrying of light items. ["VA Careers - Pharmacy: https://youtube.com/embed/Fn_ickNBEws Major duties include but are not limited to: Coordinates all clinical and distributive functions for the Compounded Sterile/Non-Sterile Products and Hazardous Drug program. Develops and implements appropriate procedures, oversees, and assures facility compliance with USP chapters , , and other applicable laws, regulations, and standards, ensuring competency of personnel, and assuring environmental control of all compounding areas. Collaborates with the facility Quality Manager and the Chief, Infection Prevention and Control to develop a formal written CSP Safety and Quality Assurance (QA) Plan in accordance with USP , and standards. Directs and oversees activities of all assigned operational, technical, and professional personnel, assuring that all USP , and compliance requirements are met in compounding and hazardous drug management. Maintains environmental control of the sterile compounding areas, including collaboration with Biomedical/Engineering/Facilities Management Services/ Safety and CETA certified third parties to ensure that Primary Engineering Controls (PEC) and Secondary Engineering Controls (SEC) are certified in accordance with USP and USP standards. Ensures the decision to outsource CSP preparations or to prepare CSP's locally follows the VHA PBM decision making hierarchy and associated guidance and assures PBM's CSP outsourcing guidance is followed if CSP's need to be purchased. Demonstrates recognized expertise in the area of IV Admixtures, including VISTA programs and software utilized to support IV Admixture service, and has assumed extra responsibility in the area. Responsible for quality assurance audits involving the IV Admixture Program and gathers data for or performs drug use evaluations when required for the MUE Subcommittee. Work Schedule: Full Time, Various schedules that may include some holidays and weekends. Telework: Not eligible for telework. Virtual: This is not a virtual position. Functional Statement #: FS-40864-0 Relocation/Recruitment Incentives: Not Authorized Permanent Change of Station (PCS): Not Authorized"]
