Electrical Development Quality Engineer II
AbbottAbout the role
JOB DESCRIPTION:
Job Title
Electrical Development Quality Engineer II
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’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 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 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
Our location in Sylmar, CA currently has an opportunity for an Electrical Development Quality Engineer II.
This is a fully onsite role.
A Development Quality/Design Assurance Engineer assures new or modified 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 by protecting patient/user safety and meeting business needs.
As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.
WHAT YOU’LL DO:
- Execute and support on-time completion of Design Control Deliverables.
- Accountable for Electrical Design Verification and Validation planning & execution, including active cross-functional root-cause analysis investigation & resolution activities.
- Lead or support Risk Management activities from product Concept through Commercialization.
- Support electrical design test and inspection method development, and lead method validation activities.
- Ensure DHF content completion, integrity, and regulatory & standards compliance; collaboratively communicating & resolving gaps.
- Support manufacturing process development & qualification for new product commercialization and product changes.
- Support internal & external audits and audit responses.
- Support product re-certifications.
- Support the establishment of objective, measurable, discrete, and verifiable customer and product requirements.
- Support objective component specification definitions, supplied component sampling plan development, and vendor qualifications.
- Complete Document Change Request Reviews in a timely and objective manner.
- Additional duties may be identified by functional management based on the current project/business objectives.
- Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
- 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.
Required Qualifications
- Bachelor’s Degree in Engineering or Technical Field or an equivalent combination of education and work experience.
- 2 years of quality engineering experience and demonstrated use of Quality tools/methodologies
- Experience working in a broader enterprise/cross-division business unit model preferred.
- Ability to work in a highly matrixed and geographically diverse business environment. <
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