Principal Software Design Assurance Engineer

Posted 6 Days Ago
Be an Early Applicant
Plymouth, MN
110K-188K Annually
Senior level
Healthtech • Telehealth
The Role
The Principal Software Design Assurance Engineer will lead software quality assurance activities for new medical device software, ensuring compliance with regulations and standards. Key responsibilities include creating documentation, managing risk files, and implementing processes to prevent software defects while collaborating with cross-functional teams.
Summary Generated by Built In

Job TitlePrincipal Software Design Assurance Engineer

Job Description

Principal Software Design Assurance Engineer (Plymouth, MN)

The Principal Software Design Assurance Engineer will support the development, qualification, and commercialization of innovative, highly reliable, life changing medical devices and associated software.

Your role:

  • Provide Software Quality leadership for New Product Introductions (NPIs) and Sustaining product development teams for stand-alone software projects (SaMD) as well as software-related aspects of complex medical systems.
  • Supporting the creation and review of all medical device software documentation including Software Development Plans, Software Safety Classification, Software Design Verification test plans, regression plans, and associated test protocols and test reports, software issue tracking and resolution, cyber security assessments such as Data Protection, Privacy, and Security Assessments etc.
  • Leading the creation and review of risk management files to include the risk management plan, product hazard analysis, FMEA’s, Risk Management Matrix, and Benefit Risk Determination.
  • Ensuring Risk Management is effective utilizing feedback from validation, field service, post-market surveillance, manufacturing indications, CAPAs, HHAs, etc. Familiarity with ISO 14971, Risk management for medical devices and IEC 62304 Medical Device Software. Provide guidance on Quality aspects of PDLM Deliverables in addition to Design Verification/Validation.
  • Identifying, promoting, and supporting processes and tools for use in preventing software defects (e.g. tools for assessing code design robustness and performance metrics). Participate in Design Verification Planning, Protocol Review, and Report Review.
  • Understanding of all aspects of the QMS related to Design Controls. Development and status reporting of Quality and Reliability metrics during phase reviews.

You're the right fit if:

  • You’ve acquired 7+ years of related experience in the medical device industry, preferably with software products (both embedded and standalone). Class 2 software medical device experience from conception to launch required. Experience with verification and validation (V&V) nice to have. Experience implementing and using Software quality metrics is a plus.
  • Your skills include expert knowledge of IEC 62304 (Software Development Life Cycle) required, IEC 62366 (Usability) preferred; ISO 13485 & 14971 required. Knowledge of algorithm development and user interface is a plus. Cybersecurity experience preferred, not required. SaMD experience is a must have, Artificial intelligence and Machine Learning experience are a big plus.
  • You have a bachelor’s degree or higher in a related field.
  • You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.
  • You’re a technical expert with strong communication skills, and effective in a matrixed organization and cross-functional role. Minimal travel required (<5%).

How we work together

We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.

This is an office-based role.

About Philips

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

  • Learn more about our business.
  • Discover our rich and exciting history.
  • Learn more about our purpose.
  • Learn more about our commitment to diversity and inclusion.

Philips Transparency Details

The pay range for this position in Plymouth, MN is $109,515 to $187,740.

The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.   

In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered.  Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more.  Details about our benefits can be found here. 

At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case. 

Additional Information

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

Company relocation benefits will not be provided for this position.  For this position, you must reside in or within commuting distance to Plymouth, MN.

#LI-PH1

This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates.  Interested candidates are encouraged to apply as soon as possible to ensure consideration.

Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.

The Company
Alpharetta, GA
80,000 Employees
Hybrid Workplace

What We Do

Do the work of your life to help the lives of others.

As a leading health technology company, it is our purpose to improve people’s health and well-being through meaningful innovation. Our goal is to improve 2.5 billion lives per year by 2030. ​

We also strive to be the best place to work for people who share our passion, by promoting personal development, inclusion and diversity while acting responsibly towards our planet and society.

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