Cell Therapy QC Micro Associate (GMP Testing)

Bristol-Myers Squibb; United States; On-site; USD 48,000 - 59,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid company holidays

Vacation benefits

Job summary

QC Micro Associate at Bristol-Myers Squibb works on GMP testing to support product release and in-process testing. The role provides microbiological testing support, data analysis and troubleshooting across analytical methods.

Responsibilities include sample collection, incubation and data entry for environmental monitoring, plus CAPA and deviation investigations and continuous improvement projects. The shift is Sun-Wed 6AM to 4:30PM, with competitive compensation and benefits.

Qualifications

• Bachelor's degree or equivalent combination of education and experience.
• 0-2+ years in a regulated industry with GMP testing exposure.
• Experience with environmental monitoring and microbial testing is preferred.

Responsibilities

• Perform GMP lot release and in-process testing for analytical and microbiological methods.
• Collect, incubate, transfer and data enter samples for facility monitoring.
• Support CAPA, deviations/investigations and continuous improvement tasks.
• Assist implementing new assay methodologies and instruments.
• Handle ad hoc tasks and sample management as assigned.

Skills

GMP testing

Microbiological testing

Data analysis

Sample collection

Data entry

CAPA & deviation

Assay method development

Education

Bachelor's Degree or equivalent

Job description

QC Micro Associate at Bristol-Myers Squibb works on GMP testing to support product release and in-process testing. The role provides microbiological testing support, data analysis and troubleshooting across analytical methods.

Responsibilities include sample collection, incubation and data entry for environmental monitoring, plus CAPA and deviation investigations and continuous improvement projects. The shift is Sun-Wed 6AM to 4:30PM, with competitive compensation and benefits.