Quality Control Microbiology Associate: Impact & Growth

Biopharma Careers; Bothell (WA); On-site; USD 101,120,000 - 122,554,000; Full time

Benefits offered by this job

Comprehensive benefits

Flexible Time Off

Stock opportunities

Job summary

Bristol Myers Squibb is seeking a Quality Control Associate in Bothell, WA, to support QC testing of in-process, final product, and stability samples, plus environmental and facility monitoring. The role may involve documentation updates, deviations, investigations, and continuous improvement efforts.

The position requires a science-related degree and 0–2+ years of QC experience, with GMP knowledge and attention to detail. Shift is Wed-Sat 0600-1630, with competitive compensation and benefits.

Qualifications

• Bachelor’s degree in science preferred; associate degree with equivalent experience may be considered.
• 0-2+ years of relevant microbiological or QC experience or equivalent education/experience.
• Demonstrated experience in microbiological techniques and basic lab safety.

Responsibilities

• Perform routine testing of in-process, final product and stability samples.
• Perform environmental/facilities monitoring and microbiological testing.
• Review GMP documentation and perform data verification.
• Perform document revision and support CAPA investigations.
• Identify opportunities for continuous improvement.
• May train analysts on general job duties.
• Perform other tasks as assigned.

Skills

Microbiology techniques

Documentation and data verification

Attention to detail

Communication skills

Education

Bachelor’s degree in science

Associate degree or equivalent experience

Tools

GMP documentation

Job description

Bristol Myers Squibb is seeking a Quality Control Associate in Bothell, WA, to support QC testing of in-process, final product, and stability samples, plus environmental and facility monitoring. The role may involve documentation updates, deviations, investigations, and continuous improvement efforts.

The position requires a science-related degree and 0–2+ years of QC experience, with GMP knowledge and attention to detail. Shift is Wed-Sat 0600-1630, with competitive compensation and benefits.