Senior Staff Systems Engineer - Medical Device Systems

Abbott Laboratories

Los Angeles (CA)

On-site

USD 114,000 - 228,000

Full time

42 hours ago
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Benefits offered by this job

Travel 10% of the time

Job summary

Abbott Laboratories in Sylmar, CA is seeking a senior program leader to drive complex device development in Cardiac Rhythm Management. You will oversee programs with novelty, organize teams, verify system-level designs, and collaborate across clinical, engineering, and regulatory functions to meet business objectives.

The role requires extensive experience in engineering of implantable systems, strong ISO/FDA design control knowledge, and ability to travel.

Qualifications

  • Minimum 8 years of progressively more responsible system engineering with product development experience.
  • Experience in electrical, electro-mechanical, software, mathematical or biomedical tech for implantable systems.
  • Strong knowledge of ISO/FDA design controls and cross-disciplinary collaboration.

Responsibilities

  • Lead programs with substantial novelty and cross-discipline integration.
  • Plan and execute department strategies; frame problems, design solutions, measure success.
  • Organize and manage work to deliver programs and lead teams.
  • Design and conduct system-level characterization and verification of complex systems.
  • Serve as SME on designated systems, addressing customer needs and technologies.

Skills

Electrical systems
Electro-mechanical
Software
Mathematics
Biomedical technologies

Education

Bachelor's degree in software eng / CS or related engineering field
Advanced credential in biomedical engineering or related discipline (preferred)

Job description

Abbott Laboratories in Sylmar, CA is seeking a senior program leader to drive complex device development in Cardiac Rhythm Management. You will oversee programs with novelty, organize teams, verify system-level designs, and collaborate across clinical, engineering, and regulatory functions to meet business objectives.

The role requires extensive experience in engineering of implantable systems, strong ISO/FDA design control knowledge, and ability to travel.

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