QO Lab Analyst II (Chemistry)

Zoetis; Kalamazoo (MI); On-site; USD 40,000 - 80,000; Full time

Job summary

An established industry player is seeking a QO Laboratory Analyst to support microbiology data testing in a GMP environment. This role involves analyzing product samples, maintaining high productivity, and ensuring compliance with GMP standards. The dynamic lab environment offers opportunities for growth and skill development, making it an ideal place for those eager to learn and contribute to quality control processes. Join a team that values attention to detail and teamwork while working in a fast-paced setting where your efforts will directly impact product quality and safety.

Qualifications

• AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science preferred.
• Related experience in Quality Control is preferred but not required.

Responsibilities

• Analyze finished product samples prior to commercial release.
• Perform and document qualitative and quantitative assays on samples.

Skills

Attention to Detail

Teamwork

Willingness to Learn

Education

AAS in Chemistry

BA/BS in Chemistry

MS in Chemistry

Tools

HPLC

Dissolution

SAP

LIMS

Empower3

Job description

Role Description

The QO Laboratory Analyst supports routine testing and review of microbiology data in a GMP environment.

Responsibilities:

The QO Lab Analyst works effectively in a fast-paced, customer-oriented, team laboratory environment to analyze finished product samples prior to commercial release. This is a dynamic, growing lab within a growing manufacturing site, offering opportunities to learn new skills and work cross-functionally.

1. Performs, documents, and checks records of qualitative and quantitative assays on samples.
2. The primary technologies in this lab are HPLC and dissolution.
3. Interprets and evaluates data for accuracy, precision, trends, and GMP impact.
4. Recommends and executes process improvements to continually enhance laboratory performance.
5. Maintains high productivity, multitasks effectively, and demonstrates attention to detail with a low error rate.
6. Displays flexibility and engagement in a changing environment.
7. Demonstrates good laboratory technique to prevent cross-contamination or misidentification of samples.
8. Follows written procedures accurately.
9. May train others as skills and knowledge permit.
10. Troubleshoots instrumentation as skills allow.
11. Participates in laboratory investigations as needed.
12. Supports manufacturing QC activities such as cleaning verification.

Shift Hours: 7:00am - 3:30pm. Overtime may occasionally be required.

Qualifications:

• AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science preferred.
• Related experience in Quality Control is preferred but not required.
• Experience with GMP documentation, drug formulation, in-plant laboratory, Incoming Inspection, SAP, LIMS, HPLC, Dissolution, and Empower3 is preferred.
• Key qualities include willingness to learn, teamwork, and attention to detail.
• Ability to lift less than 35 lbs occasionally.
• Must not be Cephalosporin/Penicillin sensitive.

This is a full-time, regular colleague position.

Note: Unsolicited resumes from third parties will be considered Zoetis property. Zoetis is an equal opportunity employer and provides accommodations for individuals with disabilities. All applicants must have or obtain authorization to work in the US. For inquiries, contact [e-mail].