Quality Analyst - Quality Operations Virology Laboratory 1st Shift

Zoetis•Lincoln, NE

4d•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. Schedule and conduct virology assays to support manufacturing activities, product release, and compliance/stability studies while following GLP, QO and Regulatory procedures. Hours: 1st Shift. Overtime, weekends, and holidays may be required.

Requirements

Bachelor's degree in biological sciences/chemistry
One to two years relevant experience
Experience with mammalian cell culture and basic virology techniques
Competent using Window-based applications.
Basic virology and microbiology techniques and knowledge.
Aseptic technique
Excellent Organization, Verbal, and Written Communication skills.

Nice To Haves

Experience working with Mammalian Cell Culture and Viral Assays
GLP documentation

Responsibilities

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.
Maintaining testing reagents and supplies
Assist/Perform assigned laboratory testing.
Understand and perform basic laboratory techniques/procedures as per training and SOPs.
Apply current Good Manufacturing Practices (cGMP) to assigned work.
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.
Initiate maintenance Work Orders when needed.
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.