QO Lab Analyst IV-VII

Zoetis; Kalamazoo (MI); On-site; USD 42,000 - 64,000; Full time

Job summary

Zoetis in Kalamazoo, MI is seeking a QO Lab Analyst to support quality operations by analyzing raw materials, APIs, and finished products in a fast-paced laboratory setting.

Responsibilities include performing and documenting assays, interpreting data for accuracy and GMP impact, and maintaining high productivity with minimal errors. Training colleagues, participating in investigations, and learning new techniques are also part of the role.

Qualifications

• AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science.
• A minimum of 2 years related experience in Quality Operations is preferred.
• Proficiency in at least one high complexity technology (e.g., HPLC, uHPLC, GC) or 2+ lower complexity technologies.

Responsibilities

• Performs, documents, record checks, and troubleshoots qualitative or quantitative assays on samples using techniques that vary from standard laboratory equipment to highly modern and automated instrumentation.
• Interprets and evaluates data in terms of accuracy, precision, trends, and GMP impact and recommends corrective action.
• High productivity and the ability to multi-task with low error rate and attention to detail.
• Demonstrates flexibility and engagement in a changing environment; avoids cross-contamination or misidentification of samples.
• Performs routine and non-routine analyses from compendial and internal sources.
• May train others as skills and knowledge allow.
• Participates in laboratory investigations as required.
• May write routine assay protocols or conduct assay/process/instrument qualifications.
• Ability to rapidly learn new skills/techniques.

Skills

Attention to detail

Multi-tasking

GMP awareness

Education

AAS/BA/BS/MS in Chemistry/Biochemistry

Tools

HPLC

uHPLC

GC

TLC

Titrations

Wet chemistry

Water testing

Job description

Role Description

Position Summary

The QO Lab Analyst position works effectively in a fast-paced, customer-oriented, team laboratory environment to analyze raw materials, APIs, and/or finished product samples in support of the company's quality program in the laboratory.

Position Responsibilities

• 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. May participate in manufacturing QC support such as cleaning verification.
• Interprets and evaluates data in terms of accuracy, precision, trends, and potential GMP impact and recommends appropriate corrective action where necessary.
• High productivity and the ability to multi-task coupled with a low error rate and attention to detail are critical characteristics of this position.
• Demonstrates 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.
• May train others as skills and knowledge allow.
• Participates in laboratory investigations as required.
• May be responsible for writing routine assay protocols or conducting assay, process, or instrument qualifications.
• The successful candidate must also have demonstrated the ability to quickly learn new skills/techniques.

Education and Experience

• AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science.
• A minimum of 2 years related experience in Quality Operations is preferred.

Technical Skills Required

• The successful candidate must have demonstrated proficiency in at least one high complexity technology (e.g. HPLC, uHPLC, GC, advanced spectroscopy, etc.) or at least 2 or more low to medium complexity technologies (e.g. TLC, titrations, wet chemistry/physical testing, water testing, etc.) as required by the business unit.
• Job duties involve occasional lifting (less than 35 lbs), reaching, and sitting while working at computer terminal.
• Colleague will work in a facility that manufactures Cephalosporins and must not be Cephalosporin sensitive.

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.