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Supplier Quality Engineer

Abbott Diagnostics Scarborough

This is a Contract position in Boulder, CO posted May 9, 2022.

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 109,000 colleagues serve people in more than 160 countries.

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 countriesAbout AbbottThe key to successful treatment and full recovery is often fast, accurate diagnosis.

Abbott’s life-changing tests and diagnostic tools provide insights that enable smarter, faster decisions and transform the way the world is managing health.Our pioneering technology spans the world of healthcare operations
– with medical diagnostic instruments, tests, automation and informatics solutions for hospitals, reference labs, blood centers, emergency departments, physician offices and clinics.The position of Supplier Quality Professional is within our Infectious Disease Developed Markets business unit located at Scarborough, Maine.

In this role you will perform daily activities required to ensure that all purchased or otherwise received materials, products and services that can impact the quality of product or service provided conform to predefined requirements and quality attributes.

If you seek a dynamic role where your contributions will pave the way in developing new products, systems, and processes, come work with usWHAT YOU’LL DOMaintain the Supplier Quality Function, working closely with and supporting Purchasing and the New Product Development and Engineering team(s).Respond in a timely and professional manner to internal and external suppler requests that pertain to quality.Manage supplier changes through the change management system.Review Supplier Validation Protocols to ensure they meet regulatory and customer requirementsWork closely with the engineering team to schedule and drive and review purchased product first article inspections, capability studies, gage R, etc.

Investigate and drive to completion root cause analysis of product quality issues and defects for new and sustaining purchased products and implement solutions to resolve issues; assist other personnel, as required, with the Corrective Action process specific to purchased components and/or servicesManage the Supplier corrective action process, drive improvement to the ASLUtilize supplier Scorecards/metrics and analytical tools to quantify performance levels of individual suppliers and work with those suppliers to develop improvement plans to achieve quality performance goalsEstablish and execute priorities to achieve expectationsIdentify and implement continual improvement opportunities to streamline quality systems and processes.Perform external audits, as required, based on the published audit schedule and/or as needed if suppliers are struggling to achieve established quality metrics.

Other duties as requiredEDUCATION AND EXPERIENCE YOU’LL BRINGRequiredBS in Engineering, Manufacturing, Biology or related discipline or equivalent combination of education and experience.2 years’ experience in medical device industry, preferably in Quality or Supplier Engineering.

Demonstrated proficiency using Microsoft Word, PowerPoint, and ExcelPreferredFamiliarity with federal and other regulations, e.g.

QSR’s, ISO 13485, CMDR, IVDD/IVDR.

Working knowledge of the General Provisions of 21 CFR Part 11 for Electronic Records and Electronic Signatures preferred.High level of proficiency in Microsoft Office Suite of software applications is required.High level of attention to detail and accuracy is required.Strong organizational skills and ability to prioritize tasks is required.Exceptional documentation and technical writing skills is required.Excellent verbal and written English language skills is required.Ability to establish and maintain strong, effective working relationships with internal employees and external customers is required.Ability to react quickly and adapt to changes in priorities, circumstances and direction is required.Must be able to reason independently and work with minimum supervision.Ability to interpret data and make sound judgments based on those interpretations is required.Must be able to adapt to quickly changing priorities and schedules.Ability to maintain good working relationships with all co-workers and outside contracts is required.WHAT WE OFFER At Abbott, you can have a good job that can grow into a great career.

We offer:Training and career development, with onboarding programs for new employees and tuition assistanceFinancial security through competitive compensation, incentives and retirement plansHealth care and well-being programs including medical, dental, vision, wellness and occupational health programsPaid time off401(k) retirement savings with a generous company matchThe 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: http://www.abbottbenefits.com/pages/candidate.aspxFollow 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.

An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce.

JOB FAMILY:Operations Quality DIVISION:ARDx Abbott Rapid Diagnostics LOCATION:United States > Scarborough : 10 Southgate Rd ADDITIONAL LOCATIONS:WORK SHIFT:Standard TRAVEL:Not specified MEDICAL SURVEILLANCE:Not Applicable SIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday) 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