Principal Systems/Verification Engineer (Aesthetic Med Device) (Bothell, WA)

Bausch Health Companies Inc.; Bothell (WA); On-site; USD 115,000 - 158,000; Full time

Benefits offered by this job

Competitive base salary

Annual bonus or sales incentive

Health insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

401(k) match

Paid time off

Tuition reimbursement

Job summary

A leading health company in Bothell seeks a Principal Engineer to develop and verify systems for medical devices. The ideal candidate has extensive experience designing electromechanical systems and is proficient in programming languages such as C# and C++. Applicants should have strong problem-solving skills and be familiar with compliance standards. Competitive salary offers and additional benefits are included.

Qualifications

• At least 10 years of experience designing, validating, and testing complex electromechanical systems.
• 5+ years experience in medical devices.
• Proficiency in verification tools and defect tracking.

Responsibilities

• Develop system and software verification tests for medical devices.
• Lead design and code reviews on embedded Linux and Windows CE.
• Write test protocols, scripts, and reports.

Skills

System engineering concepts

Embedded platforms (Windows CE, Embedded Linux)

C#

C++

.NET

Visual Basic

MATLAB

Communication

Teamwork

Problem-solving

Education

BS or MS in Engineering

Tools

DOORS

TestTrack

JIRA

MS Project

Oscilloscopes

Logic analyzers

Job description

Principal Engineer – Aesthetic Medical Device (Bothell, WA)

Apply to the Principal Engineer – Aesthetic Medical Device role at Bausch Health Companies Inc.

Responsibilities

• Develop system and software verification tests using C, C++ and C# for medical devices.
• Lead design and code reviews and coordinate design verification testing on embedded Linux and Windows CE platforms.
• Write test protocols, scripts and reports; perform regression analysis and maintain traceability with requirements management tools (e.g., DOORS).
• Identify and analyze defect root causes, conduct testing, and collaborate with cross‑functional teams to determine corrective actions.
• Support project planning and use scheduling software such as MS Project.
• Ensure compliance with FDA Quality System and Design Control requirements, ISO 13485, IEC 14971, IEC 60601, and EN IEC 62304.

Qualifications

• BS or MS in Engineering and at least 10 years of experience designing, validating, and testing complex electromechanical systems, with 5+ years in medical devices.
• Strong knowledge of system engineering concepts and experience with embedded platforms (Windows CE, Embedded Linux).
• Proficiency in C#, .NET, C++, Visual Basic, or MATLAB.
• Experience with verification tools and defect tracking (TestTrack, JIRA).
• Demonstrated ability to use requirements management tools (DOORS/DOORS NG).
• Experience in risk management, usability engineering (EN IEC 62366), and compliance with QSR and ISO 13485.
• Excellent communication, teamwork, and problem‑solving skills.

Additional Requirements

• Travel to local sites occasionally (short duration trips).
• Work with test equipment such as oscilloscopes and logic analyzers.

Benefits

Competitive base salary ($115K‑158K) plus annual bonus or sales incentive, health, dental, vision, life, disability, 401(k) match, paid time off, tuition reimbursement, and other standard benefits.

Equal Opportunity Employer

We are an Equal Opportunity Employer. EOE Disability/Veteran. We are committed to building diverse teams and fostering an inclusive workplace.