Quality Operations Technician

Zoetis; Lincoln; On-site; GBP 25,000 - 45,000; Full time

Job summary

A leading company in animal pharmaceuticals is hiring for a Quality Assurance position at their Lincoln facility. The role requires providing critical support for manufacturing operations, ensuring compliance through real-time batch record reviews. Candidates should possess substantial experience in manufacturing or quality operations, with strong communication and organizational skills being essential.

Benefits

Sign on Bonus of $500

4 weeks paid vacation and 13 paid holidays

401(k) match with profit sharing

Tuition reimbursement and Student Loan repayment program

Comprehensive health benefits starting day 1

Qualifications

• High school diploma or equivalent required with at least 4 years of relevant experience.
• Minimum 3-5 years of progressive experience at the OTE Lead level or above.
• Demonstrated knowledge of SAP is preferred.

Responsibilities

• Perform routine batch record review functions for assigned support areas.
• Track reviews and releases to support metrics for functional QA area.
• Work with QA Operations Compliance Specialists to complete and document process checks.

Skills

Communication

Detail-oriented

Organizational skills

Teamwork

Education

High school diploma or equivalent

Relevant experience (4+ years)

3-5 years in Manufacturing or Quality Operations

Tools

SAP

Job description

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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 starting day 1.

Position Summary

This position provides Quality Assurance support for Lincoln manufacturing operations, supporting shared time between the B1 Virus Production and Biological Process Manufacturing (BPM) manufacturing process teams. This position is responsible for providing on-the-floor Quality Assurance support functions for virus production, and formulation, filling/lyophilization/capping operations by performing for real-time batch record reviews and process checks of manufacturing operations. This position reports to the Team Leader Quality Assurance Operations B1/Pharma and will interact frequently with manufacturing colleagues and area Team Leads.

Hours: 1st shift, may require off-shift availability, as needed.

Position Responsibilities

1. Perform routine batch record review functions for assigned support areas within established timelines (e.g., at the end of the shift), ensuring compliance with all applicable regulatory requirements and product registrations.
2. Track reviews and releases to support metrics for the functional QA area.
3. Work with QA Operations Compliance Specialists to complete and document manufacturing area process checks and audits.
4. Other responsibilities as assigned.

Education and Experience

Job level based on years of relevant experience:

For the GJL 020-1 level

• High school diploma or equivalent required with at least 4 years of relevant experience.

For the GJL 020-2 level

• Minimum 3-5 years of progressive experience at the OTE Lead level or above, in Manufacturing or Quality Operations.

Technical Skills and Competencies Required

Minimum Qualifications :

• Strong written and oral communication and ability to work effectively on a team.
• Process and detail oriented with the ability to follow processes.
• Demonstrated organizational, administrative skills, in addition to proven skills in multi-tasking and prioritizing projects in support of standard work.
• Ability to communicate effectively with Team Members to facilitate completion requests and review from all levels to meet all deadlines.

Preferred Qualifications :

• Demonstrated knowledge and experience with SAP.
• Self-directed – can work with little or no supervision on most tasks.
• Experience in manufacturing operations, quality operations, and/or regulatory affairs.
• Previous experience with batch record reviews.
• Ability to develop solutions to routine problems following procedures.

Physical Position Requirements

• Lift materials up to 40 lbs.
• Ability to sit, stand, and walk.
• Occasional overtime work may be needed.
• Must wear appropriate PPE (Personal Protective Equipment) in manufacturing/packaging areas.