Principal, Quality Assurance

Lyell Immunopharma•Bothell, WA

1d•$150,000 - $185,000•Onsite

About The Position

Using living cells to treat – and sometimes even cure – cancer is one of the most dramatic advances in modern medicine. Patients with hematologic malignancies have been successfully treated with cell therapies. However, these profound results have not yet been achieved in patients with solid tumors, representing approximately 90% of all cancers. And for patients with hematologic malignancies, there is a need for next-generation cell therapies that can deliver increased response rates and longer duration of response. We are a clinical-stage company advancing a pipeline of next-generation CAR T-cell therapies for patients with solid tumors or hematologic malignancies. Lyell’s product candidates are enhanced with novel technology designed to generate T cells that resist exhaustion and have qualities of durable stemness in order to drive durable tumor cytotoxicity and achieve consistent and long-lasting clinical response. We were founded by cell therapy pioneers whose decades of research elevated the broader understanding of T-cell biology and its interaction with cancer. In our quest to advance next-generation CAR T-cell therapies, we have built a fully integrated company capable of discovering new technologies, translating science into therapies, manufacturing cell therapy products, and clinically evaluating them in patients. Our culture is based on Science, Respect, Collaboration, and Courage and reflects who we are, the environment we create, and our mission's urgency. This role will be based out of Bothell, Washington. The Principal, Quality Assurance is responsible for providing Quality oversight and leadership across product lifecycle activities in a cell therapy environment. This role partners closely with Manufacturing, MSAT, Process Development, and Regulatory to support process implementation, technology transfer, process improvements, process validation, and commercialization efforts including regulatory submission support for submission(s). The incumbent will serve as a Quality representative on cross-functional project teams, ensuring that product-related activities are executed in compliance with GMP requirements while supporting timelines for clinical and commercial milestones.

Requirements

Experience in cGMP clinical manufacturing required.
Experience with electronic quality management systems (e.g. deviations, CAPAs, change management) required.
Proven capability to oversee QA operations and workflows, ensuring timely execution, compliance, and alignment with organizational priorities.
Ability to work effectively both independently and cross-functionally with Manufacturing, MSAT, Regulatory, Patient Operations, Supply Chain, and external partners to set goals, develop sound project plans, monitor progress, and report results.
Excellent communication, emotional intelligence and interpersonal skills.
Curious and proactive mindset with a continuous improvement orientation; actively seeks to understand processes, identify risks, and implement sustainable quality solutions.
Fast learner, adaptable, and has the desire and ability to work in a fast-paced, start-up environment.
Excellent analytical skills and scientific/technical expertise.
BS with a minimum of 15 years experience in biochemistry, chemical engineering, bioengineering, or related scientific field; or
10-15 years of experience in GMP biopharmaceutical operations including 4 years in cell therapy and/or lentiviral manufacturing operations.
Minimum of 5+ years in Quality Assurance.

Nice To Haves

Experience with Plasmid and LVV manufacturing strongly preferred.
Direct experience supporting BLA submissions, regulatory filings, and/or health authority inspections.
Experience in commercial manufacturing and post-approval lifecycle management.

Responsibilities

Provide Quality oversight and leadership across product lifecycle activities in a cell therapy environment.
Partner with Manufacturing, MSAT, Process Development, and Regulatory to support process implementation, technology transfer, process improvements, process validation, and commercialization efforts including regulatory submission support.
Serve as a Quality representative on cross-functional project teams, ensuring that product-related activities are executed in compliance with GMP requirements while supporting timelines for clinical and commercial milestones.
Provide CDMO Quality oversight for process validation (PPQ) activities, ensuring execution aligns with approved protocols, GMP requirements, and regulatory expectations.
Review and approve validation protocols, reports, and supporting documentation (e.g., risk assessments, sampling plans, acceptance criteria, specifications).
Partner with CDMO, MSAT, and Process Development to define PPQ and validation strategies, ensuring they are robust and include evaluation of critical process parameters (CPPs), critical quality attributes (CQAs), and in-process controls.
Provide Quality oversight during PPQ execution on the manufacturing floor, ensuring adherence to protocols and real-time issue escalation.
Assess PPQ data for completeness, accuracy; ensure conclusions are justified and support process validation.
Ensure deviations occurring during PPQ and validation are appropriately investigated, documented, and resolved with minimal impact to timelines.
Ensure alignment between validation activities and regulatory filings (IND/BLA), including traceability between executed studies and submitted data.
Act as the Quality representative on cross-functional project teams supporting product development, tech transfer, process validation, IND support, and commercialization activities.
Serve as Quality Subject Matter Expert (SME) for IND and BLA coordination activities, ensuring consistency between Quality documentation and regulatory submissions.
Author and review CMC sections of regulatory submissions to ensure accuracy, completeness, and compliance with GMP requirements.
Ensure all validation, manufacturing, and quality documentation is inspection-ready and supports regulatory filings and commitments.
Drive continuous improvement initiatives to enhance process robustness, validation effectiveness, and inspection readiness.
Lead cross-functional readiness activities to ensure the manufacturing site is prepared for regulatory inspections as applicable.
Provide Quality oversight for deviations, CAPAs, and change controls, as applicable.