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:
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.
The Regulatory Inspection Manager leads end-to-end management of regulatory inspections supporting Lincoln Operations, including the White Hall, IL site. These manufacturing sites produce sterile vaccines, monoclonal antibodies, and non-sterile pharmaceuticals for animal health. The role serves as the primary coordinator and point of contact with Health Authorities and in-country Zoetis Regulatory Managers, with primary inspection interfaces including the EU, FDA, and additional global markets as applicable. USDA interactions are coordinated through a dedicated USDA liaison. This role plans, prepares for, hosts, and drives closure of regulatory inspections to ensure compliant outcomes, timely commitments, and sustained inspection readiness. The role is manager-level and operates as an individual contributor (no direct reports), leveraging strong matrix leadership across site functions and above-site teams.
Hours: 1st Shift, 7:30am - 4:00pm.
Position Responsibilities
Regulatory inspection leadership (end-to-end)
Inspection planning and readiness
Inspection execution / hosting
Post-inspection response and closure
Global procedure ownership and site alignment
Regulatory intelligence and gap assessment
Governance, quality systems, and continuous improvement
Auditing and inspection readiness activities
Qualifications (Required)
· Bachelor's degree in a scientific, engineering, or related discipline (or equivalent experience).
· Demonstrated experience leading and coordinating regulatory inspections in a GMP-regulated environment.
· Required: familiarity with sterile vaccine, monoclonal antibody, and non-sterile pharmaceutical manufacturing facilities and the primary regulatory bodies supporting the site (EU, FDA, USDA) and applicable global markets.
· Strong knowledge of Quality Systems (e.g., deviation investigations, CAPA, change control, document control, training, risk management).
· Proven ability to lead cross-functional teams through influence (matrix leadership) and manage multiple priorities under tight timelines.
· Excellent written and verbal communication skills, including experience drafting formal regulatory responses and executive summaries.
· Zoetis certified auditor (or ability to achieve/maintain certification per Zoetis requirements).
Qualifications (Preferred)
· Experience interacting with multiple global health authorities and inspection types.
· Supplier auditing experience.
· Experience developing inspection readiness programs and governance routines.
Technical Skills and Competencies Required
Physical Position Requirements
Full time
Regular
Colleague
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The world’s leading animal health company. We’ve been innovating ways to predict, prevent, detect, and treat animal illness for over 70 years, and we continue to stand by those raising and caring for animals worldwide – from veterinarians and pet owners to livestock farmers. Our leading portfolio and pipeline of medicines, vaccines, diagnostics and technologies make a difference in over 100 countries.
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