{"schemaVersion":"jobsearcher.job.v1","id":"c82abc5d5a96833c56d65d4b","url":"https://jobsearcher.com/jobs/c82abc5d5a96833c56d65d4b","canonicalUrl":"https://jobsearcher.com/jobs/c82abc5d5a96833c56d65d4b","title":"Documents Coordinator","description":"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.\nABOUT ABBOTT\nAbbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.\nWORKING AT ABBOTT\nAt 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:\nProduction areas that are clean, well-lit and temperature-controlled\nTraining and career development, with onboarding programs for new employees and tuition assistance\nFinancial security through competitive compensation, incentives and retirement plans\nHealth care and well-being programs including medical, dental, vision, wellness and occupational health programs, Medical Benefits start day 1\nVacation – 120 hours of accrued vacation (1st yr is prorated) + vacation buy program + 5 personal days + 10 paid holidays\nRetiree Healthcare program\nRobust 401(k) retirement savings with a generous company match\nTuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.\nA 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.\nA stable company with a record of strong financial performance and history of being actively involved in local communities\nA 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.\nOVERVIEW\nAudit and assure accuracy of batch records to be compliant with policies, procedures and regulatory requirements. Assure compliance to Federal Regulations pertaining to Low Acid Canned Foods, Infant Formula Act, Acidified Foods, Nutritional Labeling Laws, and Good Manufacturing Practices.\nWHAT YOU’LL DO\nResponsible for implementing and maintaining the effectiveness of the quality system.\nDetermine appropriate release criteria and communicate with DQA, PR&D, and 3rd Party Manufacturers on document requirements, documentation guidelines and audit discrepancies.\nInitiate Exception Reports (ERs) and Plant Information Reports (PIRs) and route for disposition.\nEnter and maintain work orders, ERs and Standard Quality Evaluations (SQEs) into the Release Batch Activity (RBA) system.\nUse of CAMBAR and AMAPS to adjust or obtain release status for specific batches.\nAudit and maintain records on non-batch related items (i.e.: Storage Temperature Logs).\nCoordinate isolations, holds, and reworks. Resolve discrepancies and deviations prior to final review.\nReconcile product inventories with the amount of product that was manufactured. Track and report quality statistics.\nAssist and backup coordinators and auditors when needed. Train and provide work for contract workers. Responsible to train new employees where needed.\nAssist Supervisor as business needs dictate. Ensure holds and isolations have been initiated and address as required and verify all sort/destruct issues are completed and documented in work order. Complete final batch review of work orders ensuring all critical items are in compliance with regulations before submission to Supervisor when needed.\nEnter corrections and correction plans into GQMS.\nCoordinate product impact brackets as needed.\nAssist with the coordination of the surveillance testing program at the plant.\nCoordinate and communicate release timing of batches to meet release goals.\nAssist with completion of Certificates of Analysis.\nResponsible for coordinating and documentation of Surveillance testing, hold actions and rework and release of product.\nErrors can result in FDA observations, Corporate Compliance Audit Observations, OSHA, Recall or other regulatory action.\nDemands excellent time management and organizational skills to meet deadlines.\nProduct must be released by the target launch date or shipment to customers may be delayed and in turn can negatively impact wholesale and retail business.\nCustomer dissatisfaction and possibly loss of customer accounts could also result if a late batch release were to deplete product inventory.\nREQUIRED QUALIFICATIONS\nHigh School Diploma / GED\nMinimum 2 years of QA experience\nKnowledge of applicable regulatory standards and requirements for infant formula and nutritionals.\nThorough knowledge of the manufacturing process including Analytical, Processing, Filling and familiarity with FDA and IFA regulations.\nAbility to analyze and trouble shoot complex problems and question data.\nStrong communication and writing skills\nProficient in computer applications\nAbility to prioritize workload to meet business needs\nPREFERRED QUALIFICATIONS\nBachelor’s degree in a technical field preferred\n1+ year of experience as a Batch Records Coordinator\nA thorough knowledge and ability to audit all batch records preferred.\nApply Now\nIn 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)\nLearn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com\nEmployees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.\nFollow 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 and a Military/Veteran friendly Employer, committed to employee diversity.\nConnect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.\n\nThe base pay for this position is $19.05 – $38.15 per hour. In specific locations, the pay range may vary from the range posted.","company":"Abbot","rawCompany":"abbot","city":"Columbus","state":"OH","isRemote":false,"isActive":false,"createdAt":"2026-07-27T13:39:47.879Z","occupations":[{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"15-1299.03","title":"Document Management Specialists","slug":"document-management-specialists"}],"industries":[{"code":"561410","title":"Document Preparation Services","slug":"document-preparation-services"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"311991","title":"Perishable Prepared Food Manufacturing","slug":"perishable-prepared-food-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Documents Coordinator","description":"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.\nABOUT ABBOTT\nAbbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.\nWORKING AT ABBOTT\nAt 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:\nProduction areas that are clean, well-lit and temperature-controlled\nTraining and career development, with onboarding programs for new employees and tuition assistance\nFinancial security through competitive compensation, incentives and retirement plans\nHealth care and well-being programs including medical, dental, vision, wellness and occupational health programs, Medical Benefits start day 1\nVacation – 120 hours of accrued vacation (1st yr is prorated) + vacation buy program + 5 personal days + 10 paid holidays\nRetiree Healthcare program\nRobust 401(k) retirement savings with a generous company match\nTuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.\nA 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.\nA stable company with a record of strong financial performance and history of being actively involved in local communities\nA 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.\nOVERVIEW\nAudit and assure accuracy of batch records to be compliant with policies, procedures and regulatory requirements. Assure compliance to Federal Regulations pertaining to Low Acid Canned Foods, Infant Formula Act, Acidified Foods, Nutritional Labeling Laws, and Good Manufacturing Practices.\nWHAT YOU’LL DO\nResponsible for implementing and maintaining the effectiveness of the quality system.\nDetermine appropriate release criteria and communicate with DQA, PR&D, and 3rd Party Manufacturers on document requirements, documentation guidelines and audit discrepancies.\nInitiate Exception Reports (ERs) and Plant Information Reports (PIRs) and route for disposition.\nEnter and maintain work orders, ERs and Standard Quality Evaluations (SQEs) into the Release Batch Activity (RBA) system.\nUse of CAMBAR and AMAPS to adjust or obtain release status for specific batches.\nAudit and maintain records on non-batch related items (i.e.: Storage Temperature Logs).\nCoordinate isolations, holds, and reworks. Resolve discrepancies and deviations prior to final review.\nReconcile product inventories with the amount of product that was manufactured. Track and report quality statistics.\nAssist and backup coordinators and auditors when needed. Train and provide work for contract workers. Responsible to train new employees where needed.\nAssist Supervisor as business needs dictate. Ensure holds and isolations have been initiated and address as required and verify all sort/destruct issues are completed and documented in work order. Complete final batch review of work orders ensuring all critical items are in compliance with regulations before submission to Supervisor when needed.\nEnter corrections and correction plans into GQMS.\nCoordinate product impact brackets as needed.\nAssist with the coordination of the surveillance testing program at the plant.\nCoordinate and communicate release timing of batches to meet release goals.\nAssist with completion of Certificates of Analysis.\nResponsible for coordinating and documentation of Surveillance testing, hold actions and rework and release of product.\nErrors can result in FDA observations, Corporate Compliance Audit Observations, OSHA, Recall or other regulatory action.\nDemands excellent time management and organizational skills to meet deadlines.\nProduct must be released by the target launch date or shipment to customers may be delayed and in turn can negatively impact wholesale and retail business.\nCustomer dissatisfaction and possibly loss of customer accounts could also result if a late batch release were to deplete product inventory.\nREQUIRED QUALIFICATIONS\nHigh School Diploma / GED\nMinimum 2 years of QA experience\nKnowledge of applicable regulatory standards and requirements for infant formula and nutritionals.\nThorough knowledge of the manufacturing process including Analytical, Processing, Filling and familiarity with FDA and IFA regulations.\nAbility to analyze and trouble shoot complex problems and question data.\nStrong communication and writing skills\nProficient in computer applications\nAbility to prioritize workload to meet business needs\nPREFERRED QUALIFICATIONS\nBachelor’s degree in a technical field preferred\n1+ year of experience as a Batch Records Coordinator\nA thorough knowledge and ability to audit all batch records preferred.\nApply Now\nIn 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)\nLearn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com\nEmployees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.\nFollow 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 and a Military/Veteran friendly Employer, committed to employee diversity.\nConnect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.\n\nThe base pay for this position is $19.05 – $38.15 per hour. In specific locations, the pay range may vary from the range posted.","datePosted":"2026-07-27T13:39:47.879Z","dateModified":"2026-07-27T13:39:47.879Z","hiringOrganization":{"@type":"Organization","name":"Abbot","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Columbus","addressRegion":"OH","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"c82abc5d5a96833c56d65d4b"},"url":"https://jobsearcher.com/jobs/c82abc5d5a96833c56d65d4b"}}