QA Inspection Associate

Zoetis•Charles City, IA

7d•Onsite

About The Position

The QA Inspection Associate is accountable for review and approval of new material coming to the site. Perform assigned record reviews and reviews of other records relating to processing of components, materials and finished veterinary biologicals for comparison with approved specifications and regulatory requirements. Review and approval of investigation reports. Release of materials. Creation and verification of key documents associated with release.

Requirements

Associate Level: BA/BS with 0-2 years’ experience or 6 years relevant experience.
Specialist Level: BA/BS with 2-4 years’ experience or 8 years relevant experience
Demonstrated commitment to the Zoetis Core Beliefs
Strong commitment to product quality, customer service, and continuous improvement.
Training in Corrective Action/Preventative Action, Analytical Problem Solving and Root Cause Analysis preferred.
Basic problem-solving skills.
Excellent verbal and written communication skills, fluent in English.
Proficient with the following software programs: Word, Excel, PowerPoint, SAP, Veeva Vault, Event Tracking System (ETS)
Excellent organizational skills and strong ability to multi-task.
Willingness to positively embrace change and flexibility in adjusting to changing priorities.
Strong attention to detail, ability to work well independently and as part of a team, and to work effectively with people at all levels within the organization.
Must be able to walk, sit, or stand for long periods of time.
Must be able to reach above shoulder level, bend/stoop, kneel, push/pull, twisting, and handle/grip frequently.
Extensive computer work is necessary for this position.
Ability to lift 50lbs.
Must be able to work scheduled 40 hours with the ability to work overtime as needed.
Repetitive motion and substantial movement of the wrists, hands, and/or fingers

Nice To Haves

ASQ, ISPE GMP Auditor Certification, or other relevant training and/or certification preferred.

Responsibilities

Review of records relating to the processing of components, materials and finished veterinary biologicals for comparison with approved specifications and regulatory requirements.
Review and approve assigned new and revised documents (e.g., specifications, procedures, processes, methods, protocols, and reports) associated with veterinary biological production and production support operations.
Participate in the preparation for and execution of foreign and domestic regulatory agency inspections.
Develop/revise, implement and maintain assigned Quality Assurance policies and procedures to ensure compliance with domestic and international regulatory and quality standards and requirements.
Assist with investigations and trouble shooting.
Quality approval of laboratory investigations and change controls.
Decisions regarding Quality impact
Creation and/or verification of key documents associated with release i.e., 20-08 forms, Australia permits, Certificates of Compliance, Certificates of Analysis, health documents, etc.