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Quality Analyst - Chemistry Control Laboratory

Job in Lincoln, Lancaster County, Nebraska, 68511, USA
Listing for: Zoetis
Full Time position
Listed on 2026-06-03
Job specializations:
  • Quality Assurance - QA/QC
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Benefits Include

  • $500 Sign on Bonus
  • 4 weeks accrued paid vacation and 13 paid holidays.
  • 401(k) match with company profit sharing.
  • Tuition reimbursement and Student Loan repayment program.
  • Great Health, personal, and family benefits starting day 1.
Position Summary

Perform analytical testing on raw materials, finished pharmaceutical, and biological products in accordance with established test procedures. Utilize analytical instrumentation, Computer Data Acquisition Systems (CDAS), and Laboratory Information Management Systems (LIMS) to ensure accurate and reliable data collection. Maintain strict compliance with Standard Operating Procedures (SOPs), Current Good Manufacturing Practices (CGMPs), Company Quality Standards, and FDA/EU regulatory guidelines. Adhere to testing schedules to manage a high volume of critical work while upholding the integrity of results.

Follow all policies and procedures related to the handling of DEA‑controlled substances, reference standards, and active pharmaceutical ingredients (APIs). Communicate effectively with lead analysts and team members to support collaborative and efficient laboratory operations.

Hours

1st Shift. Overtime, weekends, and holidays may be required.

Position Responsibilities

Under close supervision, the Quality Control Analyst will perform routine laboratory procedures using basic analytical skills in compliance with specifications in all Standard Operating Procedures and Standard Test Procedures used to support testing of raw materials, in‑process and finished pharmaceutical and biological animal health products.

  • Reagent Preparation
  • Chemical Identification
  • pH
  • Titrations
  • AA and UV/Vis
  • HPLC
  • GC
  • Analysis and Calculation of Results

Ensure compliance with Standard Operating Procedures (SOPs), CGMPs, Company Quality Standards and FDA/EU Guidelines. Adhere to testing schedules to accomplish a high volume of critical work without compromising the integrity of the results. Communicate effectively with lead analysts and colleagues.

Education and Experience

Required:

  • Two years associate degree in chemistry or related science field
  • One to two years of relevant experience with relevant science‑based college courses.
  • Excellent organizational, written, and oral communication skills.

Preferred:

  • Bachelor's degree in chemistry or biochemistry
  • Competent use of Window‑based applications, specifically Empower, SAP, LIMS, and Excel
Technical Skills and Competencies Required

Experience in analytical chemistry testing laboratory performing wet chemistry and instrumentation including HPLC, GC, AA, UV/Vis, and general wet chemistry experience preferred. Excellent organization, verbal, and written communication skills.

Physical

Position Requirements

Physical Demands:

  • Ability to lift 20–50 pounds routinely, exposure to temperature.
  • Withstand long periods of standing.
  • Manual dexterity using hands and fingers.
  • Specific vision abilities required by this job include close vision work.
  • Ability to reach with hands and arms.
  • Able to work flexible hours, work weekend and overtime.
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