Quality Systems Document Coordinator
AbbottAbout the role
JOB DESCRIPTION:
Quality Systems Document Coordinator
Working at Abbott
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:
- Production areas that are clean, well-lit and temperature-controlled
- Training and career development, with onboarding programs for new employees and tuition assistance
- Financial security through competitive compensation, incentives and retirement plan
- Health care and well-being programs including medical, dental, vision, wellness and occupational health programs, Medical Benefits start day 1
- Vacation – 120 hours of accrued vacation (1st yr is prorated) + vacation buy program + 3 personal days + 10 paid holidays
- Retiree Healthcare program
- Robust 401(k) retirement savings with a generous company match
- Tuition reimbursement, the Freedom 2 Save student debt program and FreeU 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 around the world and named one of the most admired companies in the world by Fortune.
- A stable company with a record of strong financial performance and history of being actively involved in local communities
- 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.
The Opportunity
This position works out of our Tipp City, OH location in the Abbott Nutrition division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® – to help them get the nutrients they need to live their healthiest lives.
Tipp City, Ohio, is one of Abbott’s newest nutrition manufacturing facilities with technology that enhances production efficiency and product quality. Join us and you’ll be part of a family that’s dedicated to innovation and excellence and dedicated to nourishing millions of families around the world.
What You'll Work On
- Implement and maintain the effectiveness of the quality system
- Update, track, issue, and implement all Master Work Orders and all other quality-related documents (including QA controlled forms, Labeling Material changes, procedures, policies, Deviations, lab methods, acceptance programs, etc.) in accordance with the Quality Assurance Document Policy.
- Assure Work Orders are issued with correct specifications, critical factors, formulation, and packaging materials
- Print, verify, and distribute to the various manufacturing departments of batch specific plant production Work Orders
- Ensure Work Orders and all other documentation are up to date and correct thus preventing the possibility of an FDA observation, Corporate Compliance Audit observation, product recall, or the possibility of serious errors that could adversely affect the nutritional efficacy, physical or microbiological stability of the manufactured product
- May perform LIMS test mapping for Analytical testing <
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