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Specialist QA Document Control

Company: Abbott Laboratories
Location: Des Plaines
Posted on: January 9, 2021

Job 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 107,000 colleagues serve people in more than 160 countriesSpecialist QA Document ControlAt Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world - in nutrition, diagnostics, medical devices and branded generic pharmaceuticals - that create more possibilities for more people at all stages of life. Today, 99,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve.At Abbott Molecular, we realize the potential of personalized care as the laboratory's most trusted and preferred source for molecular diagnostic solutions. We are a division of Abbott Laboratories, a global, diversified healthcare innovator with a legacy of pioneering work in medical diagnostics.This position is responsible for organizing and maintaining the Abbott Molecular (AM)Document Control System and the AM Design Records System (DRS) to meet currentregulatory requirements. Position Responsibilities:* Reviewing and processing change requests for new documents and revisions to existingdocuments and securing and controlling access of documentation as required byprocedures and regulations.* Ensuring that any new documents or changes to existing documents are appropriate,justified, and approved by the required functional areas according to established* * Coordinating documentation with new product teams and successfully completingassigned projects.Position Accountabilities:* Accountable for the integrity and maintenance of the AM Division Document Control and* Record Retention system, including both electronically and manually. Includes storageand retention of the Division's documents and records.* Accountable for the integrity and maintenance of electronic design records in a designrecords database.* Interact with all levels and functional areas of the Am organization including R&D,* Manufacturing, Quality, Purchasing, Planning, Marketing, Medical Writing, etc. andexternal organizations including external auditors and the FDA.* Responsible for ensuring that procedures are established, followed, and maintained incompliance with documented procedures and regulations.* Make day-to-day document control and change control decisions following establishedprocedures and guidelines without prior review with immediate manager.* Effectively communicate to appropriate level of management for decisions that requireEducational / Skills/ Experience:BA/BS degree preferred in science, Business, or related field to ensure accuracy oftechnical information used by manufacturing and research organizations and by theAbbott Molecular Division and regulated by the FDA and other outside agencies.The minimum knowledge, skills, and experience requirements of the position include:Advanced word processing experience with working knowledge of Microsoft OfficeApplications including Word, Powerpoint, and Excel.Exceptional organization skills with the ability to manage multiple tasks and prioritizeaccordingly.Must demonstrate high attention to detail; strive for zero errors.Must demonstrate exceptional customer service aptitude.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 (Include for Manufacturing roles only)* 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 communitiesLearn more about our benefits that add real value to your life to help you live fully: www.abbottbenefits.comFollow 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.

Keywords: Abbott Laboratories, Des Plaines , Specialist QA Document Control, Other , Des Plaines, Illinois

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