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UPMC Specialty Lab Technologist, IMCPL in Pittsburgh, Pennsylvania

Join the Life-Changing Team at UPMC Hillman Cancer Center!

Are you ready to make a difference? UPMC Hillman Cancer Center is your gateway to impactful work in the fight against cancer. As an internationally recognized leader, we’re on a mission to prevent, detect, diagnose, and treat cancer. And we need you to be part of our team!

Specialty Lab Technologist Opportunity:

  • Location: IMCPL (Immunologic Monitoring and Cellular Products Laboratory) at Shadyside and Southside Riviera sites (Pittsburgh, PA)

  • Schedule: Full-time (40 hours/week) Daylight Hours

  • Mission: Deliver high-quality and safe cellular therapies

  • Impact: Transform scientific breakthroughs into cancer care

What You’ll Do:

  • Perform advanced laboratory testing and processing

  • Manufacture cellular therapy products for patient treatment

  • Utilize cutting-edge techniques and advanced instrumentation

Join the UPMC Hillman Cancer Center family and take the first step on your laboratory career ladder. Make a difference where it matters most.

Apply Today!

  • This position is part of a UPMC Laboratory Career Ladder. The incumbent will be hired into the appropriate level based on their current education and experience level.

.Responsibilities:

  • Perform all responsibilities according to the philosophy of the UPMC Health System such that the needs of our customers are fulfilled.

  • Interact with all laboratory customers courteously and professionally.

  • Adhere to established laboratory and hospital policies in areas of procedures, protocols, methods, quality control, quality assurance, safety, compliance and personnel policies.

  • Collect background information for testing/experiments/production; initiate paperwork, perform test set-up; work area, and equipment.

  • Calculate and analyze assay/test results and quality control information. Investigate abnormal results according to established protocols.

  • Maintain detailed laboratory documentation of all assays and processes performed as per GDP (good documentation practices) guidelines.

  • Implement all quality controls to ensure assay and process validity; adhere to departmental safety standards in responsibly handling, processing and testing specimens and materials.

  • Use reagents and supplies in a cost-effective manner; monitor and maintain an appropriate supply inventory.

  • Maintain in-depth knowledge of techniques, principles, and instruments and their interrelationships.

  • Participate in the execution of assigned projects.

  • Participate in laboratory competency assessments and proficiencies as required.

  • Enter accurate demographic and processing information into a designated database system.

  • Perform specialized tasks which may include cellular product manufacture, tissue processing, cell culture maintenance, leukapheresis processing, blood processing and cryopreservation, in-process testing (ELISA, flow cytometry, cell sorting, viral titer, cytokine production, mycoplasma and endotoxin testing) and immune monitoring.

  • Follow cGMP (current good manufacturing practices) guidelines in the production of cellular products.

  • BS degree in a relevant scientific field required

  • Ability to use independent judgement to problem-solve

  • Experience in cell culture and sterile technique preferred

  • Experience in tissue processing a plus

  • Experience performing complex assays a plus

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