QA Compliance Specialist (Veterinary Manufacturing)

Zoetis, Inc; Charles City (IA); Vor Ort; USD 65.000 - 90.000; Vollzeit

Zusammenfassung

Zoetis, Inc is seeking a Quality Assurance professional for a full-time role in Charles City, Iowa. You will collaborate with manufacturing colleagues to oversee investigations, perform batch-record reviews, and support regulatory inspections while ensuring compliance with GMP and internal policies.

The role requires strong CAPA and root cause analysis skills, proficiency with SAP and MS Office, and excellent English communication. Travel may be necessary as part of the QA activities.

Qualifikationen

• BA/BS in a relevant field; 0–2 years for Associate or 2–4 years for Specialist.
• CAPA, Analytical Problem Solving and Root Cause Analysis preferred; basic problem-solving skills.
• Excellent verbal and written communication in English.
• Proficient with SAP, Word, Excel, and PowerPoint.
• Excellent organizational skills and ability to multitask.
• Willingness to embrace change and adjust to priorities.
• Travel may be required.

Aufgaben

• Tracking documents to ensure timely review for release.
• Review and approve SOPs to maintain compliance.
• Perform batch record reviews.
• Prepare for and participate in regulatory inspections (foreign and domestic).
• Develop/revise and maintain QA SOPs.
• Audit manufacturing processes for compliance with licenses.
• Review documentation and collect site metrics data.
• Support all QA areas and release-related items.
• Review and approve deviations and related action items.

Kenntnisse

CAPA

Analytical problem solving

Root cause analysis

Verbal communication

Written communication

Team collaboration

Travel may be required

Ausbildung

BA/BS degree in a relevant field

Tools

SAP

Word

Excel

PowerPoint

Jobbeschreibung

Zoetis, Inc is seeking a Quality Assurance professional for a full-time role in Charles City, Iowa. You will collaborate with manufacturing colleagues to oversee investigations, perform batch-record reviews, and support regulatory inspections while ensuring compliance with GMP and internal policies.

The role requires strong CAPA and root cause analysis skills, proficiency with SAP and MS Office, and excellent English communication. Travel may be necessary as part of the QA activities.