QC Micro Associate, Cell Therapy – Early Career

Bristol-Myers Squibb; Bothell (WA); On-site; USD 73,000 - 89,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid company holidays

Vacation allowance

Job summary

Bristol Myers Squibb is seeking a QC Micro Associate for a Sun-Wed, 6AM to 4:30PM shift in Bothell, WA. The role focuses on GMP testing to support product release and in-process testing, with technical support for microbiological assays.

Requirements include a Bachelor's degree or equivalent and 0-2+ years of regulated industry experience. Join a team that emphasizes quality, compliance, and professional growth.

Qualifications

• Bachelor’s Degree or equivalent combination of education and experience.
• 0-2+ years of regulated industry experience or equivalent education/experience.
• Perform GMP lot release and in-process testing for analytical and/or microbiological test methods.
• Quality Control and Environmental Monitoring of environmental and microbiological testing.
• Complete sample collection, incubation, transferal, and data entry supporting facility monitoring.
• Support document revisions, CAPA and deviation/investigation related tasks.
• Assist in the implementation of new assay methodologies and instruments.

Responsibilities

• Perform GMP testing to support product release and in-process testing.
• Provide technical support and troubleshooting for microbiological tests.
• Support CAPA and deviation/investigation tasks and continuous improvement efforts.
• Assist in implementing new assay methodologies and related instruments.
• Perform sample management duties as assigned.

Skills

GMP testing

Microbiological testing

Data analysis

Environmental Monitoring

Sample collection

Education

Bachelor’s Degree or equivalent

Tools

Electronic instruments

Computer systems

Job description

Bristol Myers Squibb is seeking a QC Micro Associate for a Sun-Wed, 6AM to 4:30PM shift in Bothell, WA. The role focuses on GMP testing to support product release and in-process testing, with technical support for microbiological assays.

Requirements include a Bachelor's degree or equivalent and 0-2+ years of regulated industry experience. Join a team that emphasizes quality, compliance, and professional growth.