Zoetis is the world's largest manufacturer and supplier of animal pharmaceuticals. Our plant in Lincoln, NE, has been recognized as one of Nebraska's safest companies, with a long-standing presence in the community. We are a clean, modern site that continues to innovate and grow.
Position Summary
Perform tasks necessary to ensure control of GMP documents utilized for Biological, Pharmaceutical, and Veterinary Medicine Research & Development operations according to current policies and procedures.
Hours: 1st Shift, 7:30am – 4:00pm. Occasional overtime may be required.
Position Responsibilities
Education and Experience
Technical Skills and Competencies Required
Preferred Candidate Qualifications
Physical Position Requirements
This position requires sitting, standing, lifting, and walking with occasional overtime.
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 zoetiscolleagueservices@zoetis.com to request an accommodation. Zoetis 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.