Associate Manufacturing Line Quality Engineer
Abbott
Scarborough, Maine
Full-Time
$50,700
HybridAssociate
Associate Manufacturing Line Quality Engineer (2nd Shift Position)
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 Scarborough, ME location in the Infectious Disease, Diagnostics Division. We’re empowering smarter medical and economic decision-making to help transform the way people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott’s diagnostics instruments, providing lab results for millions of people.
The Associate Manufacturing Line Quality Engineer (2nd shift position) is within our Infectious Disease business unit located at all sites under Abbott Diagnostics Scarborough Quality Management System (QMS). In this role you will provide support for product quality assurance, process improvements, and all quality system programs.
Working Hours: 2nd Shift Monday – Friday, 2:00 pm - 10:30 pm
What You’ll Work On
Support production with resolution of quality issues in accordance with established procedures.
Support production on the manufacturing floor, ensuring adherence to procedures and ensuring appropriate device history record (DHR) documentation. Supports line clearances, reworks, and inspections as required.
Demonstrates commitment to the development, implementation and effectiveness of Quality Management System per ISO, FDA, and other regulatory agencies.
Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
Understands and is aware of the quality consequences which may result from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities.
Other duties as assigned, according to the changing needs of the business.
Required Qualifications
Bachelor’s Degree in Engineering, Chemistry, Biotechnology, Life Science or other technical field or the equivalent Combination of education and experience.
Preferred Qualifications
Working knowledge of Database software; Internet software; Inventory software; Spreadsheet software and Word Processing software.
Working knowledge of FDA, cGMPs/QSR and ISO quality system requirements
Strong technical writing skills and effective communication skills.
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:https://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 abbott.com, on LinkedIn at https://www.linkedin.com/company/abbott-/, and on Facebook at https://www.facebook.com/AbbottCareers.
The base pay for this position is
$50,700.00 – $101,300.00In specific locations, the pay range may vary from the range posted.