Quality Technician/Analyst – Microbiology Team

ZoetisLincoln, NE
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 companion animals and livestock. Our plant has been recognized as one of 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. Position Summary Schedule and conduct Environmental Monitoring to support manufacturing activities and for product release while following GLP (Good Laboratory Practices), QO (Quality Organization) and Regulatory procedures. Preparation media for Quality Control testing to support manufacturing activities and for product release while following batch records, QO, and GLP procedures. Secondary responsibilities could require Perform routine glassware preparation, washing and sterilization in compliance with specified Standard Operating Procedures.

Requirements

  • Associate’s degree in biological sciences/chemistry
  • One to two years relevant experience.
  • Basic Aseptic technique
  • Excellent Organization, Verbal and Written Communication skills
  • Experience in media preparation and autoclave operation beneficial.
  • Basic understanding of aseptic operation and microbiology.
  • Ability to lift 20-50 pounds routinely
  • withstand long periods of standing
  • exposure to temperature.
  • Manual dexterity using hands and fingers.
  • Withstand long periods of standing.
  • Exposure to high temperatures (autoclaves)
  • Occasional need to sit, reach with hands and arms.
  • Manual dexterity using hands and fingers.
  • Specific vision abilities required by this job include close vision work.
  • Occasional need to sit, reach with hands and arms.
  • Ability to work flexible hours, work weekend and overtime
  • All applicants must possess or obtain authorization to work in the US for Zoetis.

Nice To Haves

  • Bachelor’s degree in biological sciences/chemistry
  • Experience with aseptic manufacturing environments
  • Competent using Window-based applications, specifically MODA, SAP, and Excel
  • Experience with aseptic practices and aseptic manufacturing areas
  • Knowledge of MODA SAP, LIMS, Process Runner, and Microsoft Excel.

Responsibilities

  • Schedule and conduct Environmental Monitoring to support manufacturing activities and for product release while following GLP (Good Laboratory Practices), QO (Quality Organization) and Regulatory procedures.
  • Prepare media for Quality Control testing to support manufacturing activities and for product release while following batch records, QO, and GLP procedures.
  • Perform routine glassware preparation, washing and sterilization in compliance with specified Standard Operating Procedures.
  • Perform routine laboratory procedures using aseptic technique, in compliance with specifications in all Standard Operating Procedures and Standard Test Procedures used to support testing and release of product.
  • Prepare aseptic and non-aseptic media for other groups within QO.
  • Perform Environmental Monitoring in production areas.
  • Monitor processes and alert supervisory personnel of known or suspected quality problems.
  • Practice basic aseptic laboratory procedures as per training and SOPs.
  • Apply Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) to assigned work.
  • Learn and demonstrate understanding of basic sterilization principles.
  • Understand and use production schedules.
  • Assist in inventory management of laboratory supplies etc.
  • Maintaining testing reagents and supplies
  • Understand and perform basic laboratory techniques/procedures as per training and SOPs.
  • Review documentation for accuracy and completeness.
  • Compile and report laboratory test results.
  • Assist in Laboratory Investigations; Alert supervisory personnel of known or suspected quality problems.
  • Contribute and participate in Continuous Improvement Projects (CIP)
  • Understand company policies and procedures, i.e., Safety, SOP’s, and cGMP’s.
  • Learn and comply with regulatory requirements such as USDA, FDA, EU
  • Demonstrate ability to perform assigned work in a safe manner.
  • Demonstrate ability to recognize potential safety hazards.
  • Verify and validate data entry in Laboratory Information Management Systems
  • Participate in trouble shooting and problem solving for routine tests and processes.
  • Demonstrate technical awareness using data, good judgment, and experience.
  • Communicate effectively between departments, shifts, and employees.
  • Routine glassware preparation
  • Washing of glassware
  • Decontaminate materials from laboratories via autoclave sterilization.
  • Sterilize glassware and other materials for use in laboratories.

Benefits

  • $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.
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