Senior Associate, Quality Assurance

Lyell Immunopharma; Bothell (WA); On-site; USD 50,000 - 62,000; Full time

Benefits offered by this job

Annual bonus

Equity Incentive Plan

Job summary

Lyell Immunopharma is seeking a Quality Assurance Senior Associate to join the LyFE manufacturing facility in Bothell, WA. The role covers batch record review, raw material disposition, deviation investigations, CAPA, change control, and other QA operations.

The position requires onsite work Sunday through Wednesday, 10 hours per day. The salary ranges from $36.00 to $45.00 hourly with potential annual bonus and equity incentives.

Qualifications

• 7+ years of experience in GMP biopharmaceutical operations or related field.
• Experience with electronic quality management systems (deviations, CAPAs, change management).
• Familiarity with batch record review and COA generation is preferred.

Responsibilities

• Execute day-to-day QA tasks to support ongoing manufacturing.
• Review and approve batch record comments and resolve discrepancies with manufacturing personnel.
• Review and approve test results and issue COAs as applicable in LIMS.
• Provide quality support for manufacturing operations in the cleanroom.
• Act as QA point of contact for process escalations and investigations.
• Review and approve lot dispositions and raw material specifications.
• Perform internal QA activities including deviation, CAPA, change control, and nonconformance reviews.
• Support process/method qualifications and validation activities.

Skills

GMP biopharma experience

Electronic quality management systems

Batch record review

Quality coordination & crossfunctional

Education

BS degree in biochemistry/chemical engineering/related field

Tools

eQMS platforms

Job description

The Quality Assurance team is seeking a highly motivated and detail-oriented Quality Assurance Senior Associate 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, and other Quality Operations functions. This role requires working a Sunday through Wednesday shift, 10 hours per day, and is an onsite role with no remote work option.

KEY RESPONSIBILITIES:

• Execute the Day-to-Day Quality Assurance Tasks to Support Ongoing Manufacturing:
• Review and approve executed electronic batch record comments and resolve discrepancies with manufacturing personnel.
• Review and approve executed test results, perform review tasks in the laboratory information management system to issue Certificates of Analysis (COAs) as applicable.
• Provide quality support for manufacturing operations in the cleanroom
• Be a quality point of contact for process support escalations, troubleshooting, triage and resolution.
• Perform routine hands-on QA activities such as intake of incoming patient apheresis and drug product pack-out activities.
• Compile, review and approve lot disposition records.
• Perform routine raw material disposition and approve raw material specifications.
• Perform review and approval of Deviation, Chage Control, CAPA, Excursion and Nonconformance record deliverables, as applicable.
• Promote a culture of safety and GMP compliance.
• Identify opportunities for continuous improvement.
• Support Process and/or Method Qualification and Validation activities by providing quality review of associated protocols, data and reports.
• Perform internal audits as
• Support operational excellence initiatives.

PREFERRED EDUCATION:

• BS degree with 7+ years experience in a relevant field (e.g. biochemistry, chemical engineering, bioengineering, or related scientific field)

PREFERRED EXPERIENCE:

• 4-6+ years of experience in GMP biopharmaceutical operations with a minimum of 2+ years in GMP quality
• Proficiency using multiple digital GMP Platforms
• Familiarity with Cellular Therapy manufacturing
• Familiarity with Lentiviral Vector manufacturing

KNOWLEDGE, SKILLS AND ABILITIES:

• Experience in clinical and cGMP manufacturing required.
• 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

The salary range for this position is $36.00 to $45.00 hourly, with the opportunity to earn an annual bonus. The salary range is an estimate, and the actual salary may vary based on Lyell's compensation practices and an applicant's qualifications and experience. Employees are also eligible to participate in Lyell's Equity Incentive Plan.

At Lyell, we believe that highest performing teams include people from a wide variety of backgrounds and experiences who respectfully challenge each other. We are committed to building an open, diverse and inclusive culture for all employees.

Lyell is proud to be an equal opportunity employer and does not discriminate on the basis of race, color, citizenship status, national origin, ancestry, sex, sexual orientation, age, religion, creed, physical or mental disability, medical condition, marital status, veteran status or any other characteristics protected under applicable federal, state and local laws.

We've learned from experience that some of the best people don't always match our requirements perfectly - if you're interested and think you could fit.