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QC Lab Analyst VI-VII

Job in Kalamazoo, Kalamazoo County, Michigan, 49006, USA
Listing for: Zoetis, Inc
Full Time position
Listed on 2026-01-01
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
Job Description & How to Apply Below

States considered:
Michigan

Role Description

The QO Lab Analyst position 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 with opportunity to learn new skills and to work cross-functionally.

  • Performs, documents and record checks qualitative and quantitative assays on samples.
  • The primary technologies in this lab are HPLC, Dissolution and KF.
  • Interprets and evaluates data for accuracy, precision, trends, and potential GMP impact.
  • Recommends and executes process improvements to continually improve laboratory performance.
  • 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.
  • Ability to follow written procedures.
  • May train others.
  • Troubleshoot instrumentation.
  • Review documentation of other analysts.
  • Participates in laboratory investigations as required.
  • As a Level VI or VII analyst, the selected candidate will be expected to contribute to the success in multiple ways including process and method improvements, training, and demonstration of efficient work practices.
  • May participate in manufacturing QC support such as cleaning verification.
  • Candidate must not be Cephalosporin/Penicillin sensitive.
SHIFT HOURS

8:00pm-4:30pm, nominally (some flexibility is allowed). Overtime may occasionally be required.

EDUCATION AND EXPERIENCE
  • AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science preferred.
  • 5 years minimum related experience in Quality Control.
  • Preferred experience includes GMP documentation, drug product formulation, in-plant laboratory, Incoming Inspection, SAP, LIMS, HPLC, Dissolution, use of Empower
    3.
  • Key characteristics of a successful candidate in this position: willingness and ability to learn, ability to work in a team environment, and attention to detail.
  • Job duties involve occasional lifting (less than 35 lbs).

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 nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers.

Individuals requiring sponsorship must disclose this fact.

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