Quality Systems Document Coordinator - Casa Grande, AZ

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:

• Career development with an international company where you can grow the career you dream of.
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with a high employer contribution
• Tuition reimbursement, the

education benefit - an affordable and convenient path to getting a bachelor's degree.

• A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

• Manage document change control activities for procedures, work orders, specifications, forms, job aids, and other quality-controlled documents.
• Create, review, revise, route, and maintain quality system documents within electronic document management systems.
• Perform batch calculations and verifications to support production schedules.
• Develop and maintain work order attachments and supporting documentation for manufacturing activities.
• Support change control and deviation implementation activities, ensuring required documentation updates are completed accurately and on time.
• Coordinate document reviews and collaborate with cross-functional teams to resolve documentation discrepancies.
• Support new product introductions (NPI), process changes, and continuous improvement initiatives affecting Quality Systems.
• Ensure formulations, packaging specifications, ingredient records, and production documentation are accurate and available before manufacturing.
• Generate reports related to document control activities, compliance requirements, and periodic reviews.
• Participate in cross-functional meetings to support production readiness and quality system compliance.
• Maintain quality records in accordance with company procedures and regulatory requirements.
• Provide backup support for Quality Systems activities and perform other duties as assigned.

• High School Diploma or GED required.
• Minimum of three years of experience in Quality Assurance, Quality Systems, Document Control, Manufacturing, Laboratory Operations, or another regulated environment.
• Working knowledge of manufacturing processes and controlled documentation practices.
• Experience reviewing technical documents with exceptional attention to detail and accuracy.
• Strong organizational, prioritization, and time management skills.
• Ability to collaborate effectively across departments and manage competing priorities.

• Associate or bachelor's degree in a scientific, technical, quality, or business-related discipline.
• Experience in food, pharmaceutical, medical device, or other regulated manufacturing environments.
• Experience using electronic document management systems such as M-Files.
• Experience with AS400 and work order management processes.
• Knowledge of change control, deviations, CAPA, and Quality Management System (QMS) processes.
• Experience supporting batch calculations, formulation changes, or production documentation.

In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire. Pre-Employment Inquiries and Citizenship | U.S. Equal Employment Opportunity Commission (eeoc.gov)