Clean Room Tech III, Ster Cmpg

Location: City of Rochester

Clean Room Tech III, Ster Cmpg page is loaded## Clean Room Tech III, Ster Cmpglocations:
Strong Memorial Hospital time type:
Full time posted on:
Posted Todayjob requisition : R266878

As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive.
** Job Location (Full Address):
** 601 Elmwood Ave, Rochester, New York, United States of America, 14642
** Opening:
** Worker Subtype:

Regular Time Type:

Full time Scheduled Weekly

Hours:

40

Department:500160 Pharmacy SMH

Work Shift:

UR - Day (United States of America)
Range:

UR URG 106 HCompensation Range:$21.36 - $29.90
* The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations.
*** Responsibilities:
** GENERAL PURPOSE Cleanroom Quality Control technicians are the highly-skilled individuals who both disinfect USP - regulated or cGMP-regulated sterile compounding environments throughout URMC pharmacy facilities, and assist with the ongoing mandated microbiological air and surface monitoring program to assure these critical compounding sites remain in microbial control, helping to ensure patient safety from contaminated compounded sterile medications. These individuals may also assist with USP Hazardous Drug Handling by implementing the environmental surface monitoring program at the discretion of the department’s Quality Management Program Director.

They coordinate and oversee technique development for new processes and supplies related to same and ensure accurate and thorough documentation and records for processes, implementing changes in collaboration with Program Director as standards dictate. It is expected that this person will be independent, self-directed and will regularly identify projects and needs of the department without having to be directly asked.

While broad goals and objectives will be defined, it is anticipated that this individual will identify and pursue the detailed projects needed to address the goals and objectives.
** ESSENTIAL FUNCTIONS
**** Environmental Monitoring:
Mandated interim internal testing program occurring “off cycle” from required outside/third-party vendor certification pharmacy cleanroom spaces and equipment
*** Areas to be tested and conditions under which testing (or retesting) must be conducted will be defined in current policy, which may be updated or revised as deemed necessary by area clean room supervisors, departmental leadership, engineering or infection control.
* ** Conducts airborne, non-viable particle count testing
** in sterile compounding clean room areas as per the schedule established by departmental policy and federal standards. + Utilizes department-owned LASAIR particle counting equipment (or other mandated/upgraded equipment per regulation or practice standards) after documented training and ongoing competency assessment(s).
* ** Conducts airborne viable particle (bioburden) testing
** in all sterile compounding clean room areas as per the schedule established by departmental policy and federal standards.
* Utilizes department-owned SAS airborne sampling equipment (or other mandated/upgraded equipment per regulation or practice standards) after documented training and ongoing competency assessment(s).
* ** Conducts*
* ** surface sample testing for viable particles
** in sterile compounding clean room areas as per the schedule established by departmental policy and federal standards.
* Utilizes specific aseptic technique to obtain high-quality surface samples on manual agar growth media plates after documented training and ongoing competency assessment(s).
** Conduct comprehensive incubation and review of…