QO Lab Analyst II (Microbiology) (1st Shift)
Zoetis
August 25, 2026
On-site
Kalamazoo, MI
Operations
POSITION SUMMARY
The QO Laboratory Analyst supports routine testing and review of microbiology data in a GMP environment, analyzing finished product samples prior to commercial release.
POSITION RESPONSIBILITIES
- Analyze raw materials, qualified utilities, APIs, and/or finished product samples to support the company quality program in the microbiology laboratory.
- Perform environmental monitoring.
- Support microbiological programs including release/stability testing, sanitization/sterilization validation, media prep, and growth promotion.
- Perform, document, record checks, and troubleshoot qualitative or quantitative assays using standard and automated instrumentation.
- Interpret/evaluate data for accuracy, precision, trends, and potential GMP impact; recommend corrective actions.
- Participate in laboratory investigations as required.
- May write routine protocols or conduct assay/process/instrument qualifications.
- May train others and recommend/execute process improvements.
TECHNICAL SKILLS REQUIREMENTS
- Proficiency in aseptic technique.
- Ability to quickly learn new skills/techniques.
- High productivity, multitasking ability, low error rate, and attention to detail.
- Flexibility/agility in a changing environment.
- Good lab technique to avoid cross-contamination or sample misidentification.
- Able to perform routine and non-routine analyses from compendial and internal sources.
EDUCATION AND EXPERIENCE
- AAS or BA/BS in Microbiology, Biology, or related science preferred.
- Previous QA/QC experience in GMP pharmaceutical manufacturing desired.
- Preferred: GMP documentation, drug product formulation, in-plant laboratory, Incoming Inspection, SAP, LIMS.
- Occasional lifting (<35 lbs). Must not be cephalosporin sensitive.
SHIFT HOURS
- May require weekends and/or holidays.
The QO Laboratory Analyst supports routine testing and review of microbiology data in a GMP environment, analyzing finished product samples prior to commercial release.
POSITION RESPONSIBILITIES
- Analyze raw materials, qualified utilities, APIs, and/or finished product samples to support the company quality program in the microbiology laboratory.
- Perform environmental monitoring.
- Support microbiological programs including release/stability testing, sanitization/sterilization validation, media prep, and growth promotion.
- Perform, document, record checks, and troubleshoot qualitative or quantitative assays using standard and automated instrumentation.
- Interpret/evaluate data for accuracy, precision, trends, and potential GMP impact; recommend corrective actions.
- Participate in laboratory investigations as required.
- May write routine protocols or conduct assay/process/instrument qualifications.
- May train others and recommend/execute process improvements.
TECHNICAL SKILLS REQUIREMENTS
- Proficiency in aseptic technique.
- Ability to quickly learn new skills/techniques.
- High productivity, multitasking ability, low error rate, and attention to detail.
- Flexibility/agility in a changing environment.
- Good lab technique to avoid cross-contamination or sample misidentification.
- Able to perform routine and non-routine analyses from compendial and internal sources.
EDUCATION AND EXPERIENCE
- AAS or BA/BS in Microbiology, Biology, or related science preferred.
- Previous QA/QC experience in GMP pharmaceutical manufacturing desired.
- Preferred: GMP documentation, drug product formulation, in-plant laboratory, Incoming Inspection, SAP, LIMS.
- Occasional lifting (<35 lbs). Must not be cephalosporin sensitive.
SHIFT HOURS
- May require weekends and/or holidays.