Design Assurance Engineer II

Reposted 3 Days Ago
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Burlington, MA, USA
In-Office
70K-90K Annually
Mid level
Biotech
The Role
The Design Assurance Engineer II role involves supporting product development and quality assurance through collaboration with R&D teams, conducting investigations, managing complaints, and ensuring compliance with regulations.
Summary Generated by Built In

Position Summary

We are seeking a Design Assurance Engineer II to join our team. The ideal candidate is a talented individual who is enthusiastic about learning while making a difference in the world. The DA Engineer will have the opportunity to contribute to a variety of Design Assurance core responsibilities, being the key QA team member on one or more product development projects, working collaboratively with the R&D teams from concept generation through manufacturing transfer, and contributing to risk management process throughout. The role also includes directing cross-functional complaint teams on investigations and root cause analysis to drive product improvement, assisting with complaint metrics and analysis, development of automated metrics system, and managing CAPAs, as required.

Primary Responsibilities

  • Contribute to new product development activity by participating in Design Assurance tasks including risk management activities, V&V planning and execution, statistical analysis, design reviews, and R&D testing.
  • Work with cross-functional complaint teams to conduct product malfunction investigations and root cause analysis to drive product improvement.
  • Assist with monthly and weekly complaint metrics and analysis. Assist with data analysis, visualization, and reporting using MS Excel and Tableau.
  • Assist with the management of the corrective and preventive action system by leading teams through the process, facilitating structured root cause analysis, and keeping CAPAs on track to target timelines
  • Execute corrective actions to solve problems and non-conformances based on root cause analysis.
  • Assist with the review of document and design changes.
  • Perform all activities in compliance with applicable regulations, Fractyl’s policies and guidelines, including, but not limited to, timely documentation of activities and maintaining all required applicable training.

Education or Certification Requirements

  • Bachelor's degree in engineering, science, or related field
Experience, Qualifications, and Skills
  • Minimum of 3-5 years of experience in design assurance/engineering roles within the medical device industry.
  • Experience with risk management methodologies (e.g., FMEA, fault tree analysis) and risk management tools.
  • Solid computer skills essential, including Microsoft Office Suite, Adobe, Minitab, etc.
  • Comfortable with basic statistics and data analysis
  • Knowledge of FDA regulations and ISO 13485 standards for medical devices
  • Experience with project management is a plus

Other Essentials and Key Success Factors

  • Strong analytical and problem-solving skills
  • Strong attention to detail and ability to prioritize tasks with a passion to deliver quality results
  • Ability to lead fast-paced projects
  • Proven and successful track record as a team-player and collaborator in small working environments
  • Excellent verbal and written communication skills
  • Highest levels of professionalism, personal values and ethical standards
Compensation

This position offers a competitive salary in the range of $62,000 – $90,000 annually, along with a comprehensive benefits package. Actual compensation will be based on relevant experience, education, and market factors.

The description and requirements outlined above are general; additional requirements may apply.


In accordance with Massachusetts law, General Laws Chapter 149, Section 19B. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.


 

Top Skills

Adobe
Microsoft Office Suite
Minitab
Excel
Tableau
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The Company
HQ: Lexington, MA
88 Employees
Year Founded: 2010

What We Do

Fractyl Health is a leader in creating innovative therapies to address the root cause of type 2 diabetes. We were founded based on groundbreaking research and biological insights showing the key role of the intestine in metabolic control. Our therapies are uniquely designed to target and control this controller for the treatment of metabolic disease. Our lead program, Revita DMR, is a first-in-class procedural therapy that is now in late-stage clinical trials for the treatment of type 2 diabetes. Our team is made up of passionate innovators at the intersection of biology and technology, working to deliver better real-world outcomes for people with metabolic disease. Fractyl is located in Lexington, Mass.

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