Quality Control Specialist - Microbiology & Compliance

Bristol-Myers Squibb; Bothell (WA); On-site; USD 109,745,000 - 132,984,000; Full time

Benefits offered by this job

Health Coverage

Wellbeing Support

Financial Well-being

Paid Time Off

Job summary

Bristol Myers Squibb Bothell, WA, is seeking a QC Specialist to support testing of in-process, final product and stability samples. The role also covers environmental monitoring, data review, and supporting method transfers and deviations.

You will train colleagues, help implement continuous improvement, and ensure compliance with GMP and regulatory expectations in a fast-paced lab environment.

Qualifications

• Bachelor’s degree or equivalent required, preferably in science.
• 2+ years of relevant analytical testing or QC experience or equivalent.
• Demonstrated experience in microbiological techniques (e.g. Gram Stain assays, sterility, environmental monitoring, endotoxin, growth promotion and aseptic technique).

Responsibilities

• Perform routine testing of in-process, final product and stability samples.
• May perform method transfer/validation and routine testing of in-process, final product, and stability samples.
• Perform data verification, data review, and review of GMP documentation for general and complex methods.
• Perform document revision.
• Identify opportunities for continuous improvement.
• Identify and initiate deviations, CAPA’s and Laboratory Investigation.
• Train and mentor others on QC test methods, processes, and procedures.
• Perform other tasks as assigned.

Skills

Analytical testing

GMP compliance

Microbiology

Documentation

Education

Bachelor's degree or equivalent

Tools

LIMS

ELN

Job description

Bristol Myers Squibb Bothell, WA, is seeking a QC Specialist to support testing of in-process, final product and stability samples. The role also covers environmental monitoring, data review, and supporting method transfers and deviations.

You will train colleagues, help implement continuous improvement, and ensure compliance with GMP and regulatory expectations in a fast-paced lab environment.