QA Specialist - Veterinary Biologics Manufacturing

6J6 - Zoetis LLC; Virginia; On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

None

Job summary

Zoetis Inc is seeking a Quality Assurance professional to lead document tracking, batch record reviews, and SOP approvals at our veterinary biology facility. The role supports regulatory inspections and deviation management, ensuring compliance with GMP and internal policies.

The ideal candidate has a BA/BS with 0–4 years of related experience (or 6–8 years for senior levels), strong English communication, and proficiency in SAP, Word, Excel, and PowerPoint.

Qualifications

• Associate: BA/BS with 0-2 years of experience or minimum 6 years relevant experience.
• Specialist: BA/BS with 2-4 years of experience or minimum 8 years relevant experience.
• CAPA, Analytical Problem Solving and Root Cause Analysis training preferred. Basic problem-solving skills.
• Excellent verbal and written communication skills, fluent in English.
• Proficient with SAP, Word, Excel, and PowerPoint.
• Excellent organizational skills and ability to multi-task.
• Willingness to adapt to changing priorities and travel may be required.

Responsibilities

• Track documents to ensure timely review and release on time.
• Review and approve Standard Operating Procedures to maintain compliance.
• Perform assigned batch record reviews.
• Participate in preparation for and execution of foreign and domestic regulatory inspections.
• Develop, revise, implement and maintain QA SOPs.
• Audit manufacturing processes for compliance against licenses.
• Conduct documentation review and data collection for site metrics.
• Support QA roles across all areas and review manufacturing/environmental/GMP deviations.
• Participate in Change Management as team member or change agent.

Skills

Verbal communication

Written communication

Multitasking

Education

BA/BS with 0-2 years

BA/BS with 2-4 years

Tools

SAP

Word

Excel

PowerPoint

Job description

Zoetis Inc is seeking a Quality Assurance professional to lead document tracking, batch record reviews, and SOP approvals at our veterinary biology facility. The role supports regulatory inspections and deviation management, ensuring compliance with GMP and internal policies.

The ideal candidate has a BA/BS with 0–4 years of related experience (or 6–8 years for senior levels), strong English communication, and proficiency in SAP, Word, Excel, and PowerPoint.