Staff Clinical Product Engineer

Abbott

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Quick summary

Work type
On-site
Location
Sylmar, CA
Salary
$114,000–$228,000 / yr
Employment
Full-time
Posted
92 days ago
Freshness
Confirmed live today

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $211k
This role $171k
$96k $279k
below market most similar roles pay here above market

This role pays less than 82% of similar roles. Most pay $181,795–$239,800 — the blue band above. At the midpoint, this role pays about $171k versus about $211k for comparable roles.

Based on 240 similar postings.

Employer

About Abbott

Abbott Laboratories is a global healthcare company that manufactures and markets a broad and diversified line of health care products including diagnostics, medical devices, nutritionals, and branded generic pharmaceuticals. Industry: Healthcare & Medical Devices

Abbott currently has 193 open roles on FindRole.

Listed pay typically runs $99,300–$198,700 across 123 roles with salary data.

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At a glance

TL;DR · Staff Clinical Product Engineer

The Staff Clinical Product Engineer joins the Cardiac Rhythm Management Division to lead a large group of engineers and scientists in managing clinical development for multiple projects. This role involves planning and implementing product development projects, providing technical leadership, and ensuring program objectives meet regulatory requirements and customer needs. Key responsibilities include defining clinical and workflow requirements, driving clinical design documentation like user needs and feature definitions, and developing pre-clinical evaluation protocols. The position requires interpreting customer data, analyzing electrograms, and testing prototypes to validate output. Candidates must possess a Bachelor’s degree in biomedical, mechanical, or electrical engineering and have at least seven years of medical device experience. The work focuses on developing smart, connected medical devices to treat heart arrhythmias and improving clinical workflows for doctors.

What you'll do

  • Lead a large group of engineers and scientists to manage clinical development for multiple projects.
  • Plan and implement product development projects while providing technical leadership and supervision to others.
  • Coordinate logistics and budgets while acting as a cross-functional liaison to meet regulatory requirements.
  • Define clinical and workflow requirements by engaging with customers throughout the product development cycle.
  • Drive clinical design documentation including user needs, feature definitions, and design validation.
  • Develop and direct pre-clinical evaluation protocols, data analysis, and reports.
  • Simulate and test new projects to validate that prototypes meet customers' intended use requirements.
  • Provide input to risk management files and Clinical Evaluation Reports throughout the product lifecycle.

What we're looking for

  • Bachelor's Degree in biomedical, mechanical, electrical, or similar engineering field, or an equivalent combination of education and work experience.
  • Minimum 7 years of progressively more responsible work experience in the medical device industry or equivalent.
  • Demonstrated ability to apply understanding of clinical applications to resolve issues within assigned projects.
  • Strong analytical, problem-solving, organizational, and quantitative skills.
  • Comprehensive written and verbal communication, interpersonal, facilitation, and presentation skills.
  • Ability to travel approximately 20%, including internationally.
  • Master’s or Doctoral Degree in biomedical, mechanical, electrical engineering, biological or physical science, or medicine (preferred).
  • Advanced credential in a relevant discipline/concentration, including Biomedical Engineering (preferred).

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