Risk Management Engineer
Listed on 2026-10-05
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Engineering
Quality Engineering
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.
This position works out of our St Paul, MN location for our Electrophysiology Medical Device business. In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.
What You’ll Work OnRisk Management Engineer II assures new products perform the functions intended in a safe manner and establishes compliance with the quality system. They collaborate with clinical, design engineering, regulatory, labeling, and post market surveillance functions to ensure that risk is appropriately mitigated, evaluated, disclosed, and monitored. They are 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.
- Product Development – support/execute risk management plan
- Support system/product risk management planning
- Support the requirements development process to assure quality of requirements and linkage to risk management file
- Support System Hazard Analysis; support risk assessments (FTAs, FMEAs);
Analyze and incorporate legacy inputs; coordinate/integrate cybersecurity risk with patient safety implications - Assure and maintain traceability among hazards, risks, risk analyses, evaluations and risk controls, and verification of implementation and effectiveness of risk controls
- Support writing of system/product risk management reports
- Be point of contact for tracking and developing response to post market signals (event‑based and periodic) and lead resulting risk management file updates
- Including annual risk file updates
- Complaint analysis and related action planning/response
- Backroom support for audits
- Risk Management Tool Mastery – develop proficiencies in primary risk assessment tools (e.g., FMEA, FTA)
- Support Risk Management Process Excellence – identify opportunities for improvement and drive/support process/infrastructure changes
- Identify/support process improvements driven by changes to external regulations, standards, or guidance or by internal Abbott Quality Policies
- Support CAPA efforts with linkages to Risk Management Process or Execution
- Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
- Bachelor level degree in Engineering or Technical Field
- 5+ years’ experience
- Previous design quality engineering experience and demonstrated use of quality tools/methodologies
- Experience working in a broader enterprise/cross‐division business unit model
- Advanced Degree
- Medi…
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