Quality Analyst – Chemistry Control Laboratory 1st Shift

Zoetis•Lincoln, NE

1d•Onsite

About The Position

Zoetis is the world’s largest Manufacturer and Supplier of Animal Pharmaceuticals. At Zoetis in Lincoln, NE, we manufacture high quality medicines for dogs, cats, and livestock. Our plant has been recognized as one of the Nebraska’s Safest Companies, with a long-standing presence in the Lincoln community. We are a clean, modern site that continues to innovate and grow. 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. Basis skills may include the following. Reagent Preparation Chemical Identification pH Water Determination 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.

Requirements

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

Nice To Haves

Bachelor’s degree in chemistry or biochemistry
Competent use of Window-based applications, specifically Empower, SAP, LIMS, and Excel

Responsibilities

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.
Reagent Preparation
Chemical Identification
pH
Water Determination
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.