Staff Quality Engineer Abbott Laboratories - 3.8 Santa Clara, CA Job Details Full-time $114,000 - $228,000 a year 1 day ago Benefits Health insurance Tuition reimbursement Retirement plan Qualifications Statistics Report preparation Technical engineering Data analysis reporting ISO standards Quality control statistical data analysis GMP Technical report writing Data-driven problem-solving Biomedical regulatory compliance Computer skills Cross-functional communication FDA regulations Full 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 122,000 colleagues serve people in more than 160 countries. Working at Abbott At 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: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree. A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune. A 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. The Opportunity This position works out of our Santa Clara, CA location in the SH division.

Structural Heart Business Mission:

Why We Exist. Our 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 Work On We are seeking an experienced, high caliber Staff Supplier Development Quality Engineer to be responsible to act as the site interface to suppliers. 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. Drives the development, maintenance and improvement of quality of implantable heart valve components sourced from outside suppliers. Reviews new heart valve components specifications and proposes changes to existing specifications to support component quality and manufacturability. Develops all supplied component quality plans to drive component qualification throughout the lifecycle of the design. Manages development of supplied product inspection procedures and first article requirements. Responsible for Supplier Quality activities such as: Supplier Audits, Supplier performance, etc. Provides engineering guidance to Abbott Receiving Inspection including statistical analysis, measurement techniques, and Gage R&R studies. Assesses supplier capabilities through direct visits, technical discussions, and directed testing. Collaborates with suppliers to develop comprehensive process validation strategies. Proactively communicates quality issues to suppliers as needed through supplier corrective action requests, data driven and technical discussions. Leads the investigation, permanent resolution and prevention of supplied component nonconformances. Responsible for Supplier Performance and Evaluation. Evaluates and develops Supplied Data Agreement, Skip Lot, Dock-to-Stock, CoC, and CoA partnerships with suppliers. Applies thorough engineering analysis and judgement to reduce the need for inspection in accordance to program policies and data gathered. Works with Manufacturing Engineering to assess and address supplied component issues. Applies systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. Participate in or lead teams in supporting Supplier Quality program requirements (e.g., represent the Supplier Quality function as a Core Team Member). Mitigates risk by work in partnership with the suppliers to document Process Flow Charts, PFMEAs, and Control Plans. Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. Performs other related duties and responsibilities, on occasion, as assigned. Required Qualifications BS degree in Engineering or Technical Field or equivalent experience; advanced degree preferred 7+ years' Engineering experience and demonstrated use of Quality tools/methodologies Detailed knowledge of

FDA, GMP, ISO 13485, ISO

14971, and

ISO 22442

Solid communication and interpersonal skills Advanced computer skills, including statistical/data analysis and report writing skills 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 Qualifications Training and/or Certification to

ISO 22442

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 Prior medical device (implantable) manufacturing experience preferred but not necessary. Experience implementing various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing) 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. Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews. The base pay for this position is $114,000.00 - $228,000.00. In specific locations, the pay range may vary from the range posted.