QO Lab Analyst IV - VII

Zoetis Spain SL; Michigan; On-site; USD 55,000 - 75,000; Full time

Job summary

Zoetis in Michigan seeks a QO Lab Analyst to analyze raw materials, in-process materials, APIs, and finished product samples in a fast‑paced, customer‑oriented laboratory environment. The role involves performing qualitative and quantitative assays with standard equipment and automated instruments, interpreting data for GMP impact, and supporting investigations and training across the lab.

Candidates should have 2+ years in Quality Operations and a degree in Chemistry/Biochemistry, with

Qualifications

• 2+ years of related experience in Quality Operations preferred.
• Proficient in at least one high‑complexity instrument (HPLC/uHPLC/GC) or multiple lower‑complexity techniques.
• Ability to write routine assay protocols or qualifications.
• Ability to learn new skills quickly and train others when needed.

Responsibilities

• Perform and document qualitative or quantitative assays on samples.
• Operate and troubleshoot instrumentation and interpret data for GMP impact.
• Support QC activities such as cleaning verification when needed.
• Participate in laboratory investigations and write routine protocols.

Skills

Attention to detail

Multi-tasking

Team collaboration

Good laboratory technique

Education

BA/BS or MS in Chemistry, Biochemistry, or related science

Tools

HPLC

uHPLC

GC

Spectroscopy

TLC

Titrations

Job description

States 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.

• 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 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 [e-mail] 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 availability of qualified US workers. Individuals requiring sponsorship must disclose this fact.

Join Zoetis – and build your career with a global animal health company dedicated to supporting its customers and their businesses.

Why Zoetis Zoetis has more than 60 years of experience in delivering innovative, high‑quality products and services that benefit our customers.

Zoetis work environment At Zoetis, we take pride in a collaborative spirit and high‑performing environment where every colleague is given room to learn and grow.

Your opportunities at Zoetis We invest in our people and offer diverse and exciting opportunities to make a difference in a growing global industry while shaping the future of animal health.

Results that matter Our colleagues make an impact by working hand‑in‑hand with those who raise and care for animals to better understand and address the unique real‑world challenges they face.