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.
Shift: Sun-Wed 1:30PM to 12:00AM Shift
PURPOSE AND SCOPE OF POSITION
Position Summary QC associate is responsible for supporting the release, stability, and in process testing of Cell Therapy clinical and commercial products within the Quality Control department. Additionally, the QC associate may assist with investigations and continuous improvement efforts.
REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities
Education
Bachelor’s Degree or equivalent combination of education and experience
Experience
0-2+ years of regulated industry experience or equivalent combination of education and experience
DUTIES AND RESPONSIBILITIES
- ✓Coordinate the logistics of sample receipt, internal testing and external testing
- ✓Deliver samples to internal testing labs prioritized by required turnaround times
- ✓Ship samples to external test labs and prepare associated paperwork.
- ✓Assemble QC test data packets for lot release.
- ✓Perform inventory maintenance
- ✓Maintain QC data files and perform data archival as required
- ✓Maintain instrumentation and supporting documentation in a GMP compliant manner
- ✓Respond to equipment alarms
- ✓Perform equipment maintenance tasks
- ✓May participate in projects and continuous improvement efforts
- ✓Communicate effectively with management regarding task completion, Roadblocks and needs.
- ✓Identify and support initiation of deviations, CAPAs and Laboratory investigations through data gathering and interview process
- ✓Micro tasks as assigned
Reporting Relationship Reports to QC supervisor, QC Micro
WORKING CONDITIONS (US Only)
The role is set in a controlled environment where the analyst will don personnel protective equipment (PPE) for personnel safety and for contamination control strategy. Analysts in this role may stand for 4-6 hours during assay performance.
This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.
This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.
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: $35.29 - $42.77per hour