QO Lab Analyst II (Microbiology) (1st Shift)

About the role

The QO Laboratory Analyst supports routine testing and review of microbiology data in a GMP environment. This position works in a fast-paced, customer-oriented, team laboratory setting to analyze finished product samples prior to commercial release. The role offers opportunities to learn new skills and collaborate cross-functionally within a dynamic, growing lab at an expanding manufacturing site.

Responsibilities

• Analyzes raw materials, qualified utilities, APIs, and/or finished product samples in support of the company's quality program in the microbiology laboratory.
• Performs environmental monitoring.
• Supports microbiological programs including release/stability testing, sanitization/sterilization validation, media prep, and growth promotion.
• Performs, documents, record checks, and troubleshoots qualitative or quantitative assays on samples using standard laboratory equipment and modern automated instrumentation.
• Interprets and evaluates data for accuracy, precision, trends, and potential GMP impact; recommends corrective action where necessary.
• Participates in laboratory investigations as required.
• May write routine protocols or conduct assay, process, or instrument qualifications.
• Trains others as skills and knowledge allow.
• Recommends and executes process improvements to enhance laboratory performance.

Requirements

• Demonstrated proficiency in aseptic technique.
• Ability to quickly learn new skills and techniques.
• High productivity, ability to multi-task, low error rate, and strong attention to detail.
• Flexibility, agility, and engagement in a changing environment.
• Good laboratory technique to prevent cross-contamination or misidentification of samples.
• Able to perform both routine and non-routine analyses from compendial and internal sources.
• Occasional lifting (less than 35 lbs).
• Must not be sensitive to Cephalosporins, as the facility manufactures them.

Qualifications

• AAS or BA/BS in Microbiology, Biology, or related science preferred.
• Previous QA/QC experience in a GMP Pharmaceutical manufacturing environment desired.
• Preferred experience includes GMP documentation, drug product formulation, in-plant laboratory, Incoming Inspection, SAP, and LIMS.

Key characteristics of a successful candidate: willingness and ability to learn, teamwork, and attention to detail.

Schedule

This position may require working weekends and/or holidays to meet business or customer needs.

Work Environment

The role involves exposure to both office settings and a manufacturing environment, including moving mechanical parts. Work conditions are 70% stationary and 30% standing/walking throughout the workday. Personal Protective Equipment (PPE) is required, including hard hats, safety ("steel-toed") shoes, eye protection, gloves, and protective clothing.

About Zoetis

Zoetis is a Fortune 500 company and the world leader in animal health, focused on discovering, developing, manufacturing, and commercializing vaccines, medicines, diagnostics, and other technologies for companion animals and livestock. The company fosters an award-winning culture centered on career growth, connection, and support for employees.

Benefits

Zoetis offers competitive healthcare and retirement savings benefits, along with a range of programs and policies supporting employee well-being, including health, financial wellness, family, and lifestyle resources.