Quality Engineer III

Abbott • Alameda, CA

1d • $100,000 - $200,000 • Onsite

About The Position

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 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. Free medical coverage for employees via the Health Investment Plan (HIP) PPO 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 This position works out of our Alameda, CA location in the Diabetes Care division where we are focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology. This position is responsible for activities related to design control, qualification, specification, and corrective and preventive action (CAPA) of medical devices, including software as a medical device (SaMD), digital platforms, and globally deployed web‑based systems supporting regulated products. The role will have a particular emphasis on governance, design control, and quality oversight of worldwide website unification initiatives, ensuring consistent compliance, risk management, and lifecycle documentation across regions.

Requirements

• Bachelors degree in Engineering, Science, or technical related field
• Minimum 5 years applicable technical/engineering experience and demonstrated use of Quality tools/methodologies.
• Minimum 3 years regulated industry and preferable experience with design control and software as medical device.

Nice To Haves

• Experience supporting global, customer‑facing websites or digital platforms within a regulated environment, including governance of content, configuration, and release management across regions.
• Working knowledge of web technologies (HTML, CSS, JavaScript) and common content management systems or web platforms.
• Experience applying design control principles to software‑based systems, including SaMD, digital health solutions, or regulated web platforms.
• Experience collaborating cross‑functionally with R&D, IT, Regulatory, Marketing, and external partners to enable compliant deployment of digital solutions.
• Ability to provide quality oversight of third‑party or outsourced software development, including review of design documentation, validation evidence, change controls, and supplier deliverables.
• Ability to operate effectively in global organizations, influencing without direct authority and balancing regional and global quality needs.
• Strong written and verbal communication skills, with experience reviewing, approving, and defending quality and design documentation in cross‑functional and audit settings.

Responsibilities

• Drives alignment in cross functional meetings acting as QA representative on new and on market product design projects to ensure compliance with the design control process.
• Reviews and approves engineering changes in a timely manner
• Collaborates with R&D and Marketing to support mobile app deployment activities (for Software as a Medical Device projects)
• Drives alignment during cross functional review and approval of impact assessments, root-cause analysis investigation and resolution activities
• Reviews and approves batch records for products used in design verification/validation testing and clinical investigations
• Ensures Device History File (DHF) and Device Master Record (DMR) are in compliance with regulatory standards and quality management policies and procedures
• Collects, organizes, and monitors information related to quality and process improvement
• Participates in internal & external audits and ensures audit responses are submitted in a timely manner
• Leads/supports design planning efforts to include heading CFTs; establishing deliverables and tracking completion for complex projects.
• Leads/supports complex investigations and CAPA activities.

Benefits

• 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 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees