Senior Quality Engineer

February 7, 2019


Allurion Technologies is a rapidly growing, global, venture-backed healthcare company headquartered in Natick, Massachusetts with offices in Paris and Dubai. The Company was founded in 2009 by two Harvard Medical School students dedicated to helping consumers lose weight. The Company’s flagship program features the Elipse Balloon, a procedureless device for the treatment of overweight and obese consumers, an Allurion Bluetooth® body composition scale, and an Allurion smartphone app that tracks the user’s progress throughout their weight loss journey. The program leads to 25 to 30 lbs of weight loss in 4 months. The Elipse Balloon is placed in a 15-minute office visit and does not require surgery, endoscopy or anesthesia for placement or removal. The Company launched commercial operations in 2016, and 10,000 consumers have already experienced the Elipse Program. Allurion has been recognized as one of Fierce Medical Device’s Fierce 15, one of Boston’s 50onFire, and a top Emerging Technology by SAGES.



Under the direct supervision of the Director of Quality Assurance, the Sr. Quality Engineer will be responsible for supporting new product development activities and developing and implementing manufacturing processes and controls to support product quality. The qualified candidate will be a core member of the quality assurance team and will play an essential role to ensure the safety of the Elipse Device and the ongoing commercial success of Allurion.

Specifically, the Sr. Quality Engineer will be responsible for the following activities:

  • Support the development and manufacturing of Class III medical devices in conformance with the Quality System Regulation, Medical Device Directive, ISO 13485, ISO 14971, ISO 62366 and other industry related Regulations and Standards.
  • Support New Product Development activities from Concept through Launch as a Design Control Subject Matter Expert and core team member.
  • Evaluate new or modified product designs for manufacturability, serviceability, testability, reliability, and capability.
  • Assist in new product design and process changes to ensure that effective controls and requirements are established.
  • Develop process validation protocols and support process validations in accordance with applicable standards, regulations, and guidelines.
  • Lead Risk Management activities as a Subject Matter Expert in accordance with EN ISO 14971:2012.
  • Update and review existing documentation related to DHF’s, manufacturing, testing, process development, and process validation, to identify risks that could impact product quality.
  • Review and approve process changes throughout the product lifecycle. Review activities may include: verifying application of quality engineering principles during process design, verifying process testing data or reports, evaluating quality and risk documentation & metrics, and others.
  • Develop and/or revise routine procedures, work instructions, and test methods.
  • Support, create, review, and approve engineering and document change orders and implement approved changes.
  • Document all activities in compliance with applicable standards, regulations, and guidelines.
  • Monitor outgoing product quality via review of documentation such as nonconforming reports and lot history records.
  • Assist in investigations of quality issues arising from product complaints, CAPAs, and non-conforming reports.
  • Assist with internal and supplier audits.
  • Utilize problem solving tools to analyze and identify root causes and implementing corrective actions.
  • Make decisions and proposing solutions based on calculated risks identified through data analysis.


  • Bachelor’s degree, prefer technical such as engineering or biomedical.
  • Must have 3-5 years of Medical Devices experience with direct responsibilities related to Design Quality and Manufacturing.
  • Excellent interpersonal and communication skills, as well as a demonstrated ability to work well with cross functional teams.
  • Goal oriented with a positive attitude and a willingness to take initiative and solve problems creatively, independently, efficiently, and with an attention to detail.
  • Ability to handle multiple assignments in a fast-paced environment with changing priorities.
  • Ability to uphold a high standard for professionalism.
  • Confidence with Minitab, Microsoft Windows, Microsoft Office.
  • DFSS or DMAIC Black Belt Certified, preferred
  • Certified Quality Engineer (CQE), preferred
  • Certified Quality Auditor (CQA), preferred


  • Salary will be commensurate with prior experience
  • Comprehensive medical, dental, vision, life and disability insurance
  • Tuition reimbursement
  • Newborn baby care allowance
  • Generous holiday schedule
  • 3 weeks paid time off
  • Stock options
  • Company-matched 401K savings plan

Must be authorized to work in the US. 


If you are a qualified applicant, please submit your resume to:

Allurion is an equal opportunity employer.