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Scientist, QC Compliance, Cell Therapy

Job in North Bothell Area, Snohomish County, Washington, 98021, USA
Listing for: Bristol-Myers Squibb
Full Time position
Listed on 2026-09-07
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 108280 - 131212 USD Yearly USD 108280.00 131212.00 YEAR
Job Description & How to Apply Below

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.

This is work that transforms the lives of patients, and the careers of those who do it.

Position Summary

Subject matter expert leading and authoring QC deviations, laboratory investigations, CAPAs and change control. May support authoring of APQR sections for QC.

Duties/Responsibilities

Subject matter expert leading and authoring QC deviations, laboratory investigations, CAPAs and change control. Work with QC SMEs to conduct root cause analysis. Ensure timely and compliant closure of investigations, deviations, CAPAs and change controls. Generate and report KPIs. Highlight and escalation at risk items. Analyze and report CAPA effectiveness. Own document revision, project, CAPA and deviation/investigation, change management and/or continuous improvement efforts.

Train and mentor others on deviation, investigation, CAPA and change control process/procedures. Represent department in internal/ external inspections. May support authoring of APQR sections. Communicate effectively with management and cross functional teams (e.g., present investigation findings at governance forums).

Qualifications

Specific Knowledge/Skills/Abilities:
Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements. Advance problem-solving ability/mentality, critical thinking, technically adept and logical. Advance ability to communicate effectively with peers, department management and cross-functional peers about task status, roadblocks and needs. Ability to work in a fast-paced team environment, action oriented, highly organized to meet deadlines and prioritize work.

Strong mentoring, coaching, influencing, negotiating and personnel interaction skills.

Education/Experience/Licenses/Certifications

Bachelor’s degree in science, engineering, or related discipline. 6+ years of experience in biopharmaceutical or QC lab operations with 2+ years of prior investigation experience required. An equivalent combination of education and experience may substitute. Knowledge of cell therapy analytical and microbiological testing preferred. Demonstrated experience with Quality management systems. Demonstrated strong technical writing skills. Demonstrated experience in laboratory or biomanufacturing.

investigations and root cause analysis techniques preferred.

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Compensation Overview

Bothell - WA - US: $108,280 - $131,212 The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws.

Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.

Benefits
  • Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).
  • U.S.

    -based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.
  • Non-exempt employees, Rayze Bio employees, and employees located in Puerto Rico…
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