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

Zoetis; Kalamazoo (MI); On-site; USD 48,000 - 62,000; Full time

Job summary

Zoetis Kalamazoo, MI is seeking a QO Laboratory Analyst to support routine microbiology testing in a GMP environment, reviewing data and ensuring quality prior to product release. The role emphasizes aseptic technique, cross-functional teamwork, and the ability to adapt in a fast-paced lab.

You will perform environmental monitoring, assist with release testing, document results, and contribute to process improvements while training peers as skills permit.

Qualifications

• Aseptic technique proficiency and lab safety awareness.
• Ability to quickly learn new techniques and adapt to changing workflows.
• High productivity with strong attention to detail and low error rate.
• Flexibility to work in a dynamic GMP environment and team setting.
• Knowledge of cross-contamination prevention and routine/non-routine analyses.

Responsibilities

• Analyzes raw materials, APIs, and finished product samples in the microbiology lab.
• Performs environmental monitoring and supports release/stability testing.
• Documents results and troubleshoots qualitative or quantitative assays.
• Interprets data for accuracy, trends, and GMP impact; suggests corrective actions.
• Participates in lab investigations and may write routine protocols.
• Trains peers as skills allow and supports process improvements.

Skills

Aseptic technique

Learn new skills

Attention to detail

Multi-tasking

Adaptability

Education

AAS or BA/BS in Microbiology/ Biology or related science

Tools

SAP

LIMS

Job description

POSITION SUMMARY

The QO Laboratory Analyst supports routine testing and review of microbiology data in a GMP environment. The QO Lab Analyst works effectively in a fast-paced, customer-oriented, team laboratory environment to analyze finished product samples prior to commercial release. This is a dynamic, growing lab within a growing manufacturing site with opportunity to learn new skills and to work cross-functionally.

POSITION 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 techniques that vary from use of standard laboratory equipment to highly modern and automated instrumentation.
• Interprets and evaluates data in terms of accuracy, precision, trends, and potential GMP impact and recommends appropriate corrective action where necessary.
• Participates in laboratory investigations as required.
• This position may also be responsible for writing routine protocols or conducting assay, process, or instrument qualifications.
• The applicant may train others as skills and knowledge allow.
• Recommends and executes process improvements to continually improve laboratory performance.

TECHNICAL SKILLS REQUIREMENTS

• Must have demonstrated proficiency in aseptic technique.
• Ability to quickly learn new skills/techniques.
• High productivity and the ability to multi-task coupled with a low error rate and attention to detail are critical characteristics of this position.
• Must demonstrate flexibility/agility and engagement in a changing environment.
• The candidate is expected to display good laboratory technique to avoid cross-contamination or misidentification of samples.
• Able to comprehend and perform both routine and non-routine analyses from compendial and internal sources.

EDUCATION AND EXPERIENCE

• AAS or BA/BS in Microbiology, Biolology, 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, LIMS.
• Key characteristics of a successful candidate in this position: willingness and ability to learn, ability to work in a team environment, and attention to detail.
• Job duties involve occasional lifting (less than 35 lbs).
• Colleague will work in a facility that manufactures Cephalosporins and must not be Cephalosporin sensitive.

SHIFT HOURS

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

PHYSICAL REQUIREMENTS

The work environment characteristics described here are representative of those a colleague encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the colleague is regularly exposed to both office settings and a manufacturing environment, including moving mechanical parts. The work conditions for this position are 70% stationary and 30% standing and walking throughout the workday. The colleague will be required to utilize certain Personal Protective Equipment, including but not limited to, hard hats, safety ("steel-toed") shoes, eye protection, gloves, and protective clothing.

About Zoetis

At Zoetis, our purpose is to nurture the world and humankind by advancing care for animals. As a Fortune 500 company and the world leader in animal health, we discover, develop, manufacture and commercialize vaccines, medicines, diagnostics and other technologies for companion animals and livestock. We know our people drive our success. Our award-winning culture, built around our Core Beliefs, focuses on our colleagues' careers, connection and support. We offer competitive healthcare and retirement savings benefits, along with an array of benefits, policies and programs to support employee well-being in every sense, from health and financial wellness to family and lifestyle resources.