QC Operations Specialist I

Quality Control Ops Specialist I

At Gilead our pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers.

We set and achieve bold ambitions in our fight against the world's most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come.

We are seeking a highly motivated individual to join us as a Quality Control Ops Specialist I reporting to the QC analytical Sr Manager. You will work with the Quality team in supporting our efforts in this exciting new area of cancer immunotherapy.

As a QC Operations Specialist I at Gilead/Kite you will...

• Perform drug substance lot release, in‑process, and stability testing in a GMP environment, including PCR, cell‑based assays, flow cytometry and RVV/LVV stability testing.
• Execute routine laboratory testing in a GMP environment and accurately document results using KLIMS, demonstrating the ability to navigate the system effectively.
• Perform routine sampling and sample management activities, including sample aliquoting, shipping, and external submissions, while maintaining sample integrity, traceability, and chain of custody.
• Manage daily sample and reagent operations, including inventory control, organization, and traceability in compliance with GMP/GDP requirements.
• Conduct laboratory maintenance activities, including biosafety cabinet (BSC) cleaning, equipment cleaning, general lab upkeep, media preparation, reagent ordering, and laboratory stocking.
• Adhere to all GMP and GDP standards, site procedures, and safety requirements to ensure compliance and data integrity.
• Serve as a signed‑off reviewer for assigned documentation in accordance with training.
• Assist in the execution of validation and verification activities following approved protocols and procedures.
• Support quality system activities, including assistance with deviations, CAPAs, change actions, and other quality records under supervision.
• Assist in the assembly and maintenance of data trending reports, including Quality Control Metrics to support continuous improvement and compliance monitoring.
• Participate in and support training activities, including completion of required training and assistance with training documentation as needed.
• Support document revision activities with appropriate oversight.
• Capability to lift and move items weighing up to 50 lbs on an occasional basis
• Perform additional duties as assigned.

Basic qualifications:

2+ yrsBS/BA;0 yrs MS/MA

The salary range for this position is: $80,325.00 - $103,950.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. 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*.

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.