Cell Therapy QC Specialist — Impactful, Hands-On Lab Support

Bristol Myers Squibb; Bothell (WA); On-site; USD 48,000 - 59,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid company holidays

Comprehensive benefits package

Job summary

Bristol Myers Squibb is seeking a QC Associate in Bothell, WA. The role supports release, stability and in-process testing of Cell Therapy products within Quality Control. Duties include coordinating sample logistics, data packet assembly and adherence to GMP standards.

The position requires a Bachelor’s degree or equivalent and 0–2+ years of regulated industry experience. Shift: Sun-Wed 1:30PM to 12:00AM; comprehensive benefits and growth opportunities offered.

Qualifications

• Bachelor’s Degree or equivalent combination of education and experience.
• 0-2+ years of regulated industry experience or equivalent combination of education and experience.

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.

Education

Bachelor’s Degree or equivalent

Job description

Bristol Myers Squibb is seeking a QC Associate in Bothell, WA. The role supports release, stability and in-process testing of Cell Therapy products within Quality Control. Duties include coordinating sample logistics, data packet assembly and adherence to GMP standards.

The position requires a Bachelor’s degree or equivalent and 0–2+ years of regulated industry experience. Shift: Sun-Wed 1:30PM to 12:00AM; comprehensive benefits and growth opportunities offered.