About The Position

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows.

Requirements

  • Bachelor’s degree, OR Associate’s degree (AA) with 2+ years of experience working in Quality Control or biopharma laboratories, preferably in an FDA‑regulated environment, OR High School diploma with 3+ years of experience working in Quality Control or biopharma laboratories, preferably in an FDA‑regulated environment.

Nice To Haves

  • Strong working knowledge of GMP requirements as applied to QC laboratory operations.
  • Exceptional attention to detail with the ability to track and manage multiple concurrent activities and priorities.
  • Proficiency in Microsoft Office, including Excel and Visio, and related business applications.
  • Excellent verbal and written communication skills, with the ability to collaborate effectively in a team-based environment.
  • Comfortable working in a fast‑paced, small company or growth‑oriented environment, with the ability to adjust workload based on changing priorities.
  • Flexibility to adjust work schedules and work overtime as business needs require.

Responsibilities

  • Receive incoming samples, verify accompanying documentation, and accurately log sample information into the Laboratory Information Management System (LIMS).
  • Execute processes supporting sample receipt, processing, and aliquoting for release testing, stability programs, and retain samples.
  • Label, store, and organize samples in accordance with approved procedures, storage conditions, and retention requirements.
  • Coordinate and manage sample transfers and shipments to internal and external testing laboratories.
  • Perform routine cleaning, maintenance, and restocking of sample storage and laboratory support areas.
  • Collaborate with Manufacturing, Quality Assurance (QA), and Quality Control (QC) teams—including Corporate QC—to support sampling, testing, and disposition activities.
  • Manage and complete all QC-related shipping activities, ensuring compliance with safety, quality, and regulatory requirements.
  • Perform routine review of documentation, including chain-of-custody forms, processing logs, logbooks, and other QC Lab Support records.
  • Assist with deviation investigations and related documentation, as needed.
  • Provide status updates and communicate issues during daily huddles and weekly meetings.
  • Participate in Lean Lab, Operational Excellence, and continuous improvement initiatives.
  • Comply with all safety, quality, and regulatory guidelines, including GMP requirements.
  • Perform other duties as assigned to support QC operations.

Benefits

  • This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package.
  • Benefits include company-sponsored medical, dental, vision, and life insurance plans.
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service