Document Coordinator

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:

Nourish the world and your career as part of the Nutrition team at Abbott.

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®,

Glucerna® and ZonePerfect® - to help get the nutrients they need to live their healthiest life.

Casa Grande, Arizona., is one of six Abbott nutrition manufacturing plants in the U.S., with about half of its products exported around the world. Working here, you'll feel part of a family - a family of 400 that works together to help nourish the world.

WHAT YOU'LL DO

Administer document change control of Work Orders, Plant Procedures, Job Aids and other Quality Assurance controlled documents.

Perform test mapping in LIMS system for tests done in the Analytical Lab. May be required to perform minor POMsnet (electronic batch record/auditing system) recipe revisions.

Assure that quality documents are properly distributed and controlled internally.

Ensure that all necessary documents, filed processes, and other critical factors, formulations and documentation for packaging materials and ingredients are in place prior to production.

Preserve and maintain an effective system for making authorized changes to individual Work Orders and other documents.

Responsible for complying with Federal Regulations pertaining to Low Acid Canned Foods, Infant Formula Quality Control, Acidified Foods, Nutritional Labeling Laws and Good Manufacturing Practices.

Responsible for implementing and maintaining the effectiveness of the quality system.

Responsible for implementing and maintaining the effectiveness of the quality system:

Writing, updating, revising, and printing merged Work Orders and/or procedures on AS/400.

Prepare and maintain all quality-related documents, manuals, protocols, deviations, procedures, issuances, and methods that define and document the quality control system.

Updating the valid combination files associated with the Master Work Order that includes inputting and formatting the correct data into the Batch Calculation program. (per procedure)

Perform test mapping in LIMS system for tests done in the Analytical Lab.

Write, update, route, track, issue, and implement all Master Work Orders and Quality related documents in accordance with Division Quality Assurance Documents Policy. The work order and other documents must accurately reflect actual plant practices.

Coordinate changes in the labeling and packaging materials with the correct formulations as required by the Master List of Labeling Components.

Comply with department expectations.

Change control of Work Order and other QA documents. Coordinate document changes with Plant and Division representatives.

Arbitrate and resolve differences among various departments to assure that proposed changes follow the Plant, Division, and Corporate guidelines.

Perform other specific duties as assigned by the supervisor or manager, especially during the absence of other team members.

Play lead role on all issues to assure each is addressed through accurate review of in process changes for Document Coordinators prior to submission to supervisor.

Coordinating and overseeing all new products, and other new projects that involve Quality Systems.

Back up to Document Coordinators when needed.

Facilitates Deviation meeting/schedule coordination, plant Deviation implementation, Electronic Deviation coordination, Deviation follow up and close out.

Provide work orders for engineering studies, replicates, clinical as needed (attend clinical meetings, coordinate clinical work order and provide to manufacturing line.)

EDUCATION AND EXPERIENCE YOU'LL BRING

High school diploma or equivalent is required.

3 years QA related experience (ex. Lab Analyst, Batch Log Auditor, or related position) with 2 years as a Documents Coordinator preferred.

Knowledge of applicable regulatory standards and requirements for infant formula and nutritional's.

Some knowledge of manufacturing processes associated with making a batch is required.

Knowledge of the AS400 word processing system is desired.

Proficient skills with computer and management information systems.

WHAT WE OFFER

At Abbott, you can have a good job that can grow into a great career. We offer:

A fast-paced work environment where your safety is our priority

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 plans.

Health care and well-being programs including medical, dental, vision, wellness and occupational health programs.

Paid time off

401(k) retirement savings with a generous company match

The stability of a company with a record of strong financial performance and history of being actively involved in local communities.

Learn more about our benefits that add real value to your life to help you live fully: www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. Abbott is an Equal Opportunity Employer, committed to employee diversity.Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.

The base pay for this position is

$18.07 - $36.13/hour

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Operations Quality

DIVISION:

ANSC Nutrition Supply Chain

LOCATION:

United States > Casa Grande : Plant

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

No

MEDICAL SURVEILLANCE:

No

SIGNIFICANT WORK ACTIVITIES:

Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day)

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf

EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf