QO Lab Analyst IV-VII (1st Shift)

Zoetis Spain SL; Kalamazoo (MI); Hybrid; USD 55,000 - 75,000; Full time

Job summary

Zoetis Spain SL in Kalamazoo (Portage Road) seeks a QO Lab Analyst IV-VII (1st Shift) to analyze raw materials, APIs and finished products in a fast-paced GMP laboratory. You will interpret data for accuracy and GMP impact, ensure data integrity, and support QC and investigations.

Requirements include AAS/BA/BS/MS in chemistry or related science and at least 2 years in Quality Operations; experience with HPLC or TLC is preferred.

Qualifications

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

Responsibilities

• Performs qualitative or quantitative assays on samples using standard to automated instrumentation.
• Interprets data for accuracy, precision, trends and GMP impact, with corrective actions as needed.
• Maintains high productivity with low error rate and attention to detail; supports QC as needed.
• May train others and participate in laboratory investigations; writes routine assay protocols as required.

Skills

HPLC

TLC

Education

B.S./B.A./M.S. in Chemistry or related science

Job description

## QO Lab Analyst IV-VII (1st Shift)Apply: Kalamazoo - Portage Road: Full time: Posted Today: JR00021593MichiganPosition SummaryThe 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.Full timeRegularColleague