QC Lab Analyst -III; 2nd Shift

QO Lab Analyst

Job Description:

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.
• Maintains high productivity and the ability to multi‑task with a low error rate and strong attention to detail.
• Demonstrates flexibility/agility and engagement in a changing environment; displays good laboratory technique to avoid cross‑contamination or misidentification of samples.
• Comprehends and performs 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.
• Has demonstrated the ability to quickly learn new skills/techniques.

• AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science.
• Minimum of 2 years related experience in Quality Operations preferred.
• Demonstrated proficiency in at least one high‑complexity technology (e.g., HPLC, uHPLC, GC, advanced spectroscopy) or at least two low‑to‑medium complexity technologies (e.g., TLC, titrations, wet chemistry/physical testing, water testing) as required by the business unit.
• Job duties involve occasional lifting (less than 35 lbs), reaching, and sitting while working at a computer terminal.
• Colleague will work in a facility that manufactures cephalosporins and must not be cephalosporin sensitive.

Shift: 2:00 pm to 10:30 pm
Full time, Regular, Colleague

Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability.

Please contact Zoetis Colleague Services at zoeti to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of non‑immigrant status and employment eligibility, considering factors such as the availability of qualified US workers.

Individuals requiring sponsorship must disclose this fact. All applicants are eligible for reasonable accommodations and the company adheres to all anti‑hesitation and anti‑discrimination laws.