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.
Sr. Quality Engineer - 2nd Shift ($1,000 Sign-On Bonus)
Schedule: M-F 3:00 pm - 11:30 pm
About Abbott
Abbott is a global healthcare leader, creating breakthrough science to improve people\xe2\x80\x99s health. We\xe2\x80\x99re always looking towards the future, anticipating changes in medical science and technology.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You\xe2\x80\x99ll also have access to:
Career development with an international company where you can grow the career you dream of.
Free medical coverage for employees* via the Health Investment Plan (HIP) PPO.
An excellent retirement savings plan with high employer contribution.
Tuition reimbursement, the student debt program and education benefit - an affordable and convenient path to getting a bachelor\xe2\x80\x99s degree.
A company recognized as a great place to work in dozens of countries around the world 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 a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
This position works out of our Westfield, IN location in the Structural Heart division 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.
The Senior Quality Engineer will function as the regional SME providing Validation support, consultation, and training to AN manufacturing sites. This position will also interface with other regional SMEs to capture and share best practices globally.
What You\xe2\x80\x99ll Work On
Lead regional community of practice meetings to exchange best practices.
Develop and track validation related metrics.
Provide validation training and consultation services on validation policies and practices.
Work closely with regional engineering and quality personnel providing expertise and guidance for verifying and validating new products and processes.
Provide guidance on defining the validation & verification strategy, including risk management mitigations, verification and validation plans, protocols, and reports.
Review, analyze and provide recommendations for verification and validation test data.
Provide guidance on resolving deviations associated with verification and validation activities.
Solve organization problems.
Oversee recruitment and development of staff.
Required Qualifications
B.S. in Engineering, science, or similar engineering discipline
Minimum 5 years of experience in design/process verification and validation in a regulated environment such as Medical Devices, Pharmaceutical Products or Food Manufacturing.
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