Principal Engineer Aesthetic Medical Device (Bothell, WA) jobs in United States
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Bausch Health Companies Inc. · 5 hours ago

Principal Engineer Aesthetic Medical Device (Bothell, WA)

Bausch Health Companies Inc. is a global diversified pharmaceutical company dedicated to improving health outcomes for patients. The Principal Systems/Verification Engineer will be responsible for ensuring Solta products meet functional system requirements and will work collaboratively with a multi-disciplinary product development team to manage verification testing of medical devices.

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H1B Sponsor Likelynote

Responsibilities

Develop System/SW verification Tests using C, C++ and C#
Develop tests for device software, including automated tests
Lead / participate in Design and Code reviews
Demonstrated experience with Medical Device System/SW verification for Windows CE based devices and Embedded Linux based devices
Coordinate / conduct Design Verification testing (embedded Linux / C#)
Provide technical leadership / mentoring especially in applicable test methods of products
Develop plans and coordinate activities for system level verification testing, including regression analysis of system functionality to determine scope of testing, overseeing test execution and reviewing individual test results and data for inclusion with test reports
Write individual and summary level test reports which provide clear and concise results along with appropriate detail information as needed
In partnership with other system engineers, formulate system functional requirement specifications and risk assessments
Establish and maintain product requirements and verification trace management via a requirements management tool
Identify test cases and write verification test protocols for software and hardware verification/validation that utilize manual and automated test methods
Design and/or develop verification scripts to utilize automated test methods
Develop verification test scripts and protocols utilizing automated and manual test methods
Address and analyze functionality and performance related issues discovered during verification testing
Document results of work activities
Participate in defect issue tracking, troubleshooting, and resolution
Identify and isolate product defects, perform root cause analysis, and work with engineering team across design disciplines to determine corrective action
Work closely with other departments to ensure projects conform to all regulatory and quality regulations
Stay up-to-date and follow all procedures related to this job that can affect the quality of products or services provided to our customers
Be willing to travel occasionally for short duration trips

Qualification

Medical Device VerificationCC++C#Embedded SystemsRequirements ManagementFDA Quality SystemRisk ManagementUsability EngineeringTest AutomationAnalytical SkillsTeam CollaborationCommunication SkillsProblem Solving

Required

BS or MS in Engineering plus 10 years of experience designing / validating / testing of complex electro-mechanical systems, and at least five years in medical devices or closely related field
Knowledge / experience in System Engineering concepts/principles
Demonstrated experience with Medical Device System/SW verification for Windows CE based devices and Embedded Linux based devices
Proven track record of successful product testing, verification, and validation using a variety of testing tools and techniques
Ability and willingness to support project planning and management including use of scheduling software such as MS Project
Demonstrated experience on the use of a requirements management tool (e.g. DOORS/DOORS NG) for requirements trace management
Ability to focus on and achieve scheduled milestones, including contingency planning
Ability to operate test equipment such as oscilloscope, logic analyzer, etc
Strong team collaboration and communication skills
Driven to get the job done in the face of obstacles and time constraints, and a willingness to jump in wherever needed
Demonstrated ability to multi-task
Ability to read, analyze, and interpret engineering specifications, general business periodicals, professional journals, technical procedures, or governmental regulations
Ability to write reports, specifications, business correspondence, test plans / protocols and procedure manuals
Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public
Ability to clearly and concisely convey project accomplishments, obstacles, issues, and status to project team members
Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry
Ability to define problems, collect data, establish facts, and draw valid conclusions
Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables
Ability to read technical and clinical literature and documents and extract important concepts

Preferred

Experience with C# and .NET desired
Verification experience with embedded platforms including Windows CE and Embedded Linux desired
Competency in at least one of the following: C++, C#, Visual Basic, or Matlab
Use of defect tracking tools such as TestTrack, JIRA, etc
Knowledge of FDA Quality System and Design Control requirements and their application to projects from design inception to manufacturing release
Regulatory experience in QSR, ISO13485
Risk Management techniques and experience in EN 14971
Experience in Usability Engineering compliant to EN IEC 62366
Experience producing designs compliant to EN IEC 60601-1 /-2, EN IEC 62304: Medical Device Directive Essential Requirements
Working experience with ESD environment

Benefits

Comprehensive Medical (includes Prescription Drug)
Dental
Vision
Flexible Spending Accounts
401(k) with matching company contribution
Discretionary time off
Paid sick time
Tuition reimbursement
Parental leave
Short-term and long-term disability
Life insurance
Accidental death & dismemberment insurance
Paid holidays
Employee referral bonuses
Employee discounts

Company

Bausch Health Companies Inc.

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Bausch Health Companies Inc.

H1B Sponsorship

Bausch Health Companies Inc. has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (8)
2024 (7)
2023 (4)
2022 (13)
2021 (4)
2020 (5)

Funding

Current Stage
Public Company
Total Funding
$7.4B
Key Investors
Kohlberg Kravis Roberts
2025-05-21Post Ipo Debt· $2.52B
2025-03-25Post Ipo Debt· $3.08B
2023-07-07Post Ipo Debt· $600M

Leadership Team

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Thomas J. Appio
Chief Executive Officer
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Graham Jackson
SVP, Chief Quality Officer & Global Head Technical Operations
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Company data provided by crunchbase