Process Verification Specialist - mAbs

About Zoetis

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 Nebraska’s safest companies and has a long‑standing presence in the Lincoln community. We are a clean, modern site that continues to innovate and grow.

• $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

The Process Verification Specialist (PVS) will support activities within mAb operations at the Lincoln Zoetis site, including closing of lots in SAP, GMP review of batch records, audit of batch records, CAPA, and change‑management documentation. PVS will assist in area deviations when required to streamline executables and provide detailed summaries of floor events for manufacturing investigations. The candidate selected will instill a GMP culture by understanding, following, and completing process documentation in accordance with site policies and procedures.

PVS will participate in the weekend work rotation and work with QA to ensure area compliance with internal and external regulatory requirements. Area adherence to site safety policy and standards for a safe workplace are essential and will be upheld by the selected candidate.

1st shift, to be set between 7 am to 7 pm by the mAbs leadership team (M‑F, 8 hrs/day, minimum 40 hrs/week). Position requires some weekend work and is eligible for the mAbs on‑call rotation.

• Assist with batch record data assembly.
• Provide deviation pareto board updates and assist with deviation trending.
• Assist with deviation investigation and write‑up (manufacturing and environmental investigations).
• Assist with change management.
• Support related manufacturing CAPA implementation.
• Participate in daily manufacturing/Quality Assurance meeting.
• Train colleagues on GMP documentation and ensure team compliance during execution and throughout review of the batch records. Track right‑first‑time compliance.
• Act as a liaison and collaborate with manufacturing support groups (quality assurance and mAb technical support) to ensure respect of GMP practice and appropriate CAPA defined.
• Understand, follow, and complete process documentation in support of GMP.
• Understand and follow safety policies as it relates to biological and chemical components and equipment to protect personnel and maintain product quality.
• Provide production floor assistance when needed.

BS in Biological sciences, MA/MS preferred. Preference given to applicants with relevant experience in biological production. Candidates with a high school diploma and relevant experience may be considered.

• Ability to read and follow written directions.
• Ability to communicate effectively and efficiently both verbally and in writing.
• Ability to think critically.
• Ability to function independently when required.
• Ability to adapt to manufacturing needs as they occur.

• Basic computer skills (Word and Excel)
• Proficiency in SAP and ETS.
• Ability to troubleshoot and think of creative solutions.
• Familiarity with a GMP environment.

• Familiarity with biologic manufacturing process.
• Knowledge in MODA, LIMS, SAP, ETS, and databasing.
• Capable of becoming an effective trainer.

Exposure to chemicals, fumes, odors, noise, live steam, temperature fluctuations, biohazards, continuous standing and lifting to a maximum of 50 lbs.

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…