QO Lab Analyst IV - VII

Zoetis; Kalamazoo (MI); On-site; USD 60,000 - 78,000; Full time

Job summary

Zoetis Spain SL in Kalamazoo, MI seeks a QO Lab Analyst IV–VII to join a fast-paced, team‑oriented laboratory. You will analyze materials and samples using standard and automated instrumentation, ensure accuracy, and support GMP processes.

The role requires proficiency in at least one high‑complexity technology (HPLC, UHPLC, GC) or multiple lower complexity techniques, with 2+ years in Quality Operations and strong attention to detail, safety, and cross‑training ability.

Qualifications

• AAS/BA/BS/MS in Chemistry, Biochemistry, or related science.
• Minimum 2 years in Quality Operations.
• Experience with at least one high‑complexity technology (HPLC/UHPLC/GC) or 2+ low‑to‑medium complexity techniques.

Responsibilities

• Analyze raw materials, packaging materials, in-process materials, APIs, and finished product samples.
• Perform, document, and troubleshoot qualitative or quantitative assays.
• Interpret data for accuracy, precision, trends and GMP impact; recommend corrective actions.

Skills

Good laboratory technique

Attention to detail

Multi-tasking

GMP awareness

Training others

Education

AAS/BA/BS/MS in Chemistry or Biochemistry

Tools

HPLC

UHPLC

GC

Advanced spectroscopy

Titrations

Wet chemistry

Job description

## QO Lab Analyst IV - VIIApply: Kalamazoo - Portage Road: Full time: Posted Today: JR00021580States considered: Michigan The QO Lab Analyst position works effectively in a fast-paced, customer-oriented, team laboratory environment to analyze raw materials, packaging materials, in-process materials, APIs, utilities, and/or finished product samples in support of the company's quality program in the laboratory. · 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. · 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. SHIFT · 8:00 am to 4:30 pm