Documents Coordinator - 1st Shift - Altavista, VA Plantother related Employment listings - Altavista, VA at Geebo

Documents Coordinator - 1st Shift - Altavista, VA Plant

Altavista, VA Altavista, VA Full-time Full-time $18.
07 - $36.
13 an hour $18.
07 - $36.
13 an hour 10 days ago 10 days ago 10 days ago 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.
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.
Altavista, Va.
, is one of Abbott's largest nutrition manufacturing plants equipped with advanced technology to ensure efficient production.
Working here will make you feel like you're part of a family that works together to make a difference and help nourish millions of families around the world.
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 WHAT YOU'LL DO 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 that Work Orders are issued with correct specifications, critical factors, formulation, and packaging materials.
Responsible for the printing, verification, and distribution to the various manufacturing departments of batch specific plant production Work Orders.
Coordinators are responsible for ensuring that 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.
Other duties may be assigned.
May perform LIMS test mapping for Analytical testing.
Write, update, revise, and print merged Work Orders and/or procedures on the AS400 system.
Update the valid combination files associated with the Master Work Order that includes inputting and formatting the correct data into the Batch Calculation program.
Write, update, route, track, issue, and implement all Master Work Orders and Quality related documents in accordance with Division Quality Assurance Documents Policy.
Coordinate changes in the labeling and packaging materials with the correct formulations as required by the Master Specifications Manual.
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.
Review process changes accurately before submitting to Sr.
Documents Coordinator.
Assist in New Product Introduction (NPI) process to complete projects accurately and timely to continue growth of the plants portfolio.
This position is accountable for complying with applicable FDA (GMP), USDA, OSHA and Abbott regulations, policies, procedures or guidelines.
EDUCATION AND EXPERIENCE, YOU'LL BRING Required:
High School Diploma/GED.
Proficient skills with computer and management information systems are required.
Preferred:
Technical knowledge of manufacturing processes associated with making or analyzing a batch.
Knowledge of the AS400 word processing system is desired.
QA related experience (ex.
Lab Analyst, Batch Log Auditor, or related position) and 1 year as Assistant Document Coordinator preferred.
Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan.
Free coverage applies in the next calendar year.
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:
www.
abbottbenefits.
com Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life.
Abbott is an Equal Opportunity Employer, committed to employee diversity and a Military/Veteran Friendly employer.
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 per hour.
In specific locations, the pay range may vary from the range posted.
.
Estimated Salary: $20 to $28 per hour based on qualifications.

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