QA Associate Specialist: Manufacturing & Compliance Advocate

- Zoetis India Capability Center; Virginia; On-site; USD 65,000 - 90,000; Full time

Job summary

Zoetis India Capability Center is seeking a QA professional to act as a cross-functional team member and approver of Zoetis investigations for manufacturing and quality assurance activities at the site. You will review environmental monitoring data, support regulatory inspections, and perform batch record reviews to ensure compliance with specifications and regulatory requirements.

The role requires managing document tracking, SOP approvals, CAPA activities, and deviations, with emphasis on

Qualifications

• CAPA, Analytical Problem Solving and Root Cause Analysis training preferred.
• Basic problem-solving skills and strong communication.
• Excellent verbal and written communication in English.

Responsibilities

• Track documents to ensure timely release.
• Review and approve SOPs to maintain compliance.
• Perform assigned batch record reviews.
• Prepare for and execute foreign and domestic regulatory inspections.
• Develop, implement, and maintain QA SOPs.
• Audit processes for regulatory compliance.
• Documentation review and data collection for site metrics.
• Support QA roles across areas and review deviations.
• Participate in Change Management processes.
• Assist with inspections preparation and execution.

Skills

SAP

Excel

PowerPoint

Word

CAPA

Root Cause Analysis

Analytical Problem Solving

English communication

Education

BA/BS with 0-2 years experience

BA/BS with 2-4 years experience

Tools

SAP

Word

Excel

PowerPoint

Job description

Zoetis India Capability Center is seeking a QA professional to act as a cross-functional team member and approver of Zoetis investigations for manufacturing and quality assurance activities at the site. You will review environmental monitoring data, support regulatory inspections, and perform batch record reviews to ensure compliance with specifications and regulatory requirements.

The role requires managing document tracking, SOP approvals, CAPA activities, and deviations, with emphasis on