Manufacturing Process Verification Specialist – mAbs 1st shift, Lincoln
Client:
Location:
Lincoln, United Kingdom
Job Category:
Manufacturing
EU work permit required:
Yes
Job Reference:
fd3ea5247f76
Job Views:
6
Posted:
05.05.2025
Expiry Date:
19.06.2025
Job Description:
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, with a long-standing presence in the Lincoln community. We are a clean, modern site that continues to innovate and grow.
Benefits Include:
* $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.
Position Summary
The candidate will support activities within media preparation operations, including closing of processes in SAP, GMP review and audit of batch records, CAPA, and change management. Must follow GMP documentation and safety policies related to biological and chemical components and equipment. The role reports directly to the manufacturing team, with presence on the manufacturing floor expected.
Hours:
1st shift, hours between 6am to 6pm, scheduled by mAb leadership (M-F, 8-hour days, 40 hr/week).
Responsibilities:
* Review production batch records for GMP compliance and aim for 100% right first-time.
* Manage TECO and COOISPI of batches.
* Indicate change controls and update batch records accordingly.
* Assist with batch record data assembly.
* Update deviation Pareto board and assist with trending.
* Help investigate deviations and document findings, including environmental and manufacturing investigations, and manage changes.
* Implement related manufacturing CAPA.
* Participate in daily manufacturing and QA meetings.
* Train colleagues on GMP documentation and ensure team compliance.
* Collaborate with support groups to ensure GMP adherence and CAPA execution.
* Complete process documentation supporting GMP.
* Assist production tasks as needed.
* Follow safety policies related to biological and chemical hazards.
Education and Experience:
Bachelor’s degree or equivalent required; Master’s preferred. Experience in GMP-regulated manufacturing is advantageous.
Technical Skills and Competencies:
* Ability to follow written directions and communicate effectively.
* Critical thinking and independent functioning.
* Organizational skills to meet deadlines.
Technical skills include basic computer skills (Word, Excel), proficiency in SAP, troubleshooting, and knowledge of GMP, biologic manufacturing, MODA, and Trackwise.
Physical Requirements:
Exposure to chemicals, fumes, odors, noise, live steam, temperature changes, biohazards, and lifting up to 50 lbs.
Full-time, regular position.
Any unsolicited resumes sent to Zoetis will be considered property of Zoetis, and no fee will be paid for unsolicited resumes. Zoetis is an equal opportunity employer and provides accommodations for applicants with disabilities. Applicants must be authorized to work in the US; sponsorship considerations are at Zoetis’ discretion.
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