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Quality Engineer II

Company: Abbott Laboratories
Location: Saint Paul
Posted on: January 13, 2022

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 109,000 colleagues serve people in more than 160 countries.This role is weekend day shift: Wednesday or Thursday through Sunday; 8 or 10 hour days available, depending on preference. Structural Heart Business Mission: - why we existOur business purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural heart disease. -We aim to lead the markets we serve by requiring the solutions we offer customers provide an improved benefit/risk profile as compared to existing standards of care; a performance threshold that by definition, guides and ensures the productive output of our engineering, business development, and clinical research efforts result in outcomes that advance the standard of care. WHAT YOU'LL DOWe are seeking an experienced, high caliber Quality Engineer II to be responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development, manufacturing, or system/services support. Each employee can make a difference at Abbott and has the power, either individually or as a team, to influence the success of the company. We are team-oriented, fast-paced and progressive. We value people with great ideas who partner with others both internally and externally to take action and accomplish goals. This role is an individual contributor position, requiring the candidate to have comprehensive knowledge in the specific area. Seeking a candidate who:

  • Will conduct -inspection, -verification -and -validation -of -components -or -materials -used -in -development processes
  • Will be responsible for designing and maintaining programs for the systematic monitoring and evaluation of the various aspects of a project, service, or facility to ensure that standards of quality are being met.
  • Under -general -direction, -has -duties -of -instructing, -directing, -and -checking -the -work -of -other -quality assurance -professionals.
  • Will be responsible -for -application -of -quality -principles -and -complex -analysis -of -quality -records, -reports -to -form -recommendations -for -improvements.
  • Able to identify -and -address -recurring -problems -either -with -the -quality -of -the -product -or -the -reliability -of testing procedures.
  • Will document -quality -issues -and -performance -measures -for -management -review.
  • May -liaise -with -external -vendors. Impact this role will have on Abbott:
    • Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements
    • Lead in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements
    • Lead, coach, and mentor non-exempt and entry level exempt personnel
    • Assist in the development and execution of streamlined business systems which effectively identify and resolve quality issues
    • Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues
    • Design and conduct experiments for process optimization and/or improvement
    • Appropriately document experiment plans and results, including protocol writing and reports
    • Lead process control and monitoring of CTQ parameters and specifications
    • Lead and implement various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing)
    • Lead the investigation, resolution and prevention of product and process non-conformances
    • Participate in or lead teams in supporting quality disciplines, decisions, and practices (e.g., represent the Quality function as a Core Team Member)
    • Lead in the completion and maintenance of risk analysis
    • Work with design engineering in the completion of product verification and validation EDUCATION AND EXPERIENCE YOU'LL BRINGRequired
      • BS degree in Engineering or Technical Field or equivalent experience; 2-5 years' experience
      • Engineering experience and demonstrated use of Quality tools/methodologies
      • Detailed knowledge of FDA, GMP, ISO 13485, and ISO 14971
      • Solid communication and interpersonal skills
      • Strong project management and leadership skills, including the demonstrated ability to lead multi-departmental project teams and resolve quality-related issues in a timely and effective manner
      • Advanced computer skills, including statistical/data analysis and report writing skills
      • Experience implementing various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing)
      • Ability to work in a highly matrixed and geographically diverse business environment
      • Ability to work within a team and as an individual contributor in a fast-paced, changing environment
      • Ability to leverage and/or engage others to accomplish projects
      • Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization
      • Multitasks, prioritizes and meets deadlines in timely manner
      • Strong organizational and follow-up skills, as well as attention to detail
      • Ability to travel approximately 10%
      • Ability to maintain regular and predictable attendance Preferred
        • Advanced degree preferred
        • Demonstrated supervisory experience preferred
        • ASQ CQE or other certifications preferred
        • Prior medical device experience preferred
        • Experience working in a broader enterprise/cross-division business unit model preferred 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 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: - 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 , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.

Keywords: Abbott Laboratories, St. Paul , Quality Engineer II, Engineering , Saint Paul, Minnesota

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