Sr. Quality Systems/CAPA Engineer

Sr. Quality Systems/CAPA Engineer Abbott Laboratories - 3.9 Pleasanton, CA Job Details Full-time $90,000 - $180,000 a year 1 day ago Benefits Health insurance Tuition reimbursement Retirement plan Qualifications Technical engineering ISO standards GMP Biomedical regulatory compliance 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 115,000 colleagues serve people in more than 160 countries. Job Description 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 The Senior Quality Systems Engineer assures products conform to quality standards and establishes compliance with the quality system. Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success. The position employs an individual skilled in advance quality assurance techniques with an in-depth understanding of the

ISO 13485

Quality Standard and

US 21 CFR 820 QSR.

Areas of focus will include improving quality system infrastructure, performance metrics and ISO, FDA and GMP compliance. What You'll Work On Assure compliance with corporate and divisional requirements regarding metrics reporting for the Management Controls / Management Review and CAPA quality systems. Assure the collection, compiling, reporting and dissemination of key quality and compliance metrics/data are completed within the requiring timing. Complete trend analysis of data as appropriate to ensure proper actions can be determined or assessed. Perform and assure timely follow-up activities in support of key quality and compliance metric/data goals and policy/procedural requirements Develop and provide data and analysis in support of Management Controls / Management Review and CAPA Quality Systems Identify and implement opportunities for continuous improvement Identify opportunities to apply, continuously improve, and redefine quality systems and controls product-related processes in accordance with applicable internal, domestic and international quality regulations, US 21 CFR 820 (QSR), ISO 13485, etc. Represent Quality Systems as required in support of cross-functional projects Assist in company preparations for hosting external audits Participate in external and internal audits Assists management teams to ensure timely closure of audit observations. Lead non-conformance investigation teams to identify root causes and effective CAPAs Lead, coach, and mentor non-exempt and entry level exempt personnel on quality principles and procedures Function as part of risk assessment teams to identify product, quality system and compliance requirements. Function as part of special project teams to identify compliance gaps and develop and execute strategies to close gaps.

Required Qualifications :

Bachelor's degree in engineering or Technical Field Minimum 5 or more years of Engineering experience and demonstrated use of Quality tools/methodologies knowledge of

FDA820, GMP, ISO

13485, and

ISO 14971

Preferred Qualifications:

Project management and leadership skills, including the demonstrated ability to lead multi-departmental project teams and resolve quality-related issues Internal and External Audit experience MS or higher degree in a technical discipline Advanced computer skills, including statistical/data analysis and report writing skills medical device industry experience ASQ CQE or CQA certification 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 $90,000.00 - $180,000.00. In specific locations, the pay range may vary from the range posted.