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# Associate II, Quality Assurance

- **Company:** Lyell Immunopharma, Inc.
- **Location:** Seattle, WA, United States
- **Experience:** Experienced
- **Salary:** $74,880.0 - $85,280.0
- **Contract:** Permanent contract
- **Skills:** Adobe Analytics, Laboratory Information Management Systems
- **Published:** June 29, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=0388aaf1f7a8f6a3

## About the Role

Do you have experience in Quality control corrective actions?, Do you have a Bachelor's degree?, * AA/BA or BSc degree or an equivalent combination of education and work experience, * 3+ years of cGMP experience in GMP biopharmaceutical operations and with prior experience in a GMP Quality role.

 * Experience in clinical
 * Proficiency using multiple digital GMP Platforms
 * Familiarity with Cellular Therapy manufacturing
 * Familiarity with Lentiviral Vector manufacturing, * Experience with electronic quality management systems (e.g. deviations, CAPAs, change management) required.
 * Ability to work effectively both independently and with a team to set goals, develop sound project plans, monitor progress, and report results.
 * Excellent communication, emotional intelligence and interpersonal skills.
 * Motivated and organized critical thinker with solid cross-collaboration and business communication skills.
 * Fast learner, adaptable, with creative problem-solving skills.
 * Ability to work efficiently, prioritize workflow, meet deadlines and balance competing
 * The desire and ability to work in a fast-paced, start-up
 * Excellent analytical skills and scientific/technical

## Description

The Quality Assurance team is seeking a highly motivated and detail-oriented Quality Assurance Associate II to join our team at the Lyell Manufacturing Facility, LyFE in Bothell WA. This individual will perform routine Quality Assurance tasks including but not limited to batch record review, raw material disposition, deviation investigation, CAPA, and change control approval, GMP cleanroom support and other Quality Operations functions. This role requires working a shift schedule (either Sun-Wed or Wed-Sat), 10 hours per day, and is an onsite role with no remote work option., * Perform review and approval of executed electronic batch records, and resolution of discrepancies with manufacturing personnel.

 * Perform review and approval of Deviation, Excursion and CAPA record
 * Provide quality support for manufacturing operations in the cleanroom facilities (e.g. intake of incoming patient apheresis material, product pack-out, event triage).
 * Be a quality point of contact for process support escalations, troubleshooting, triage and resolution.
 * Perform review and disposition of incoming raw materials, and approval of raw material
 * Review and approve executed test results, perform review tasks in the laboratory information management system to issue Certificates of Analysis (COAs) as applicable.
 * Author and/or collaborate on the creation, revision, and obsoletion of Standard Operating Procedures across the LyFE site.
 * Perform review and approval of asset induction/release deliverables, on-demand work, and non-conformances.
 * Support other routine Quality operations as required, commensurate with experience and the LyFE site maturation.
 * Represent Quality Assurance on project specific teams, as
 * Promote a culture of safety and GMP compliance.
 * Identify opportunities for continuous improvement.
 * Perform internal audits as
 * Support operational excellence initiatives.


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