Quality Assurance Engineer - Med Device NPD
Myomo, Inc.
A leading medical device company in Burlington, MA, is looking for a Quality Assurance Engineer to support the New Product Development team. The ideal candidate will have experience in quality management within the medical device industry, demonstrating strong analytical skills and the ability to drive quality improvement projects. Responsibilities include hands-on test development, documentation reviews, and collaboration in risk management activities. This position requires a Bachelor's degree in Biomedical Engineering or a related field. #J-18808-Ljbffr Myomo, Inc.
$85k - $100k
...Quality Assurance Engineer Department: Quality Employment Type: Full Time Location: Burlington, MA Compensation... ...disabilities.) It is the only device that, sensing a patient’s own neurological... ...supports the New Product Development (NPD) team, working cross‑functionally to...SuggestedFull time- ...that are not only more effective, but also more accessible to patients around the world. The Role: The Quality Assurance Specialist II, Device Engineering will support Quality Assurance activities for Terrestrial's combination product programs, with a strong focus...SuggestedWork at office
$93k - $116k
...for an accommodation or an alternative application process. Quality Assurance Engineer II Full‑Time Regular Professionals MA Bedford CID Office,... .../ANSI standards documentation 1D and 2D Bar Code Reader Devices Magnetic Stripe Readers UV Devices RFID Readers Card Security...SuggestedFull timeTemporary workWork at officeLocal area$115k - $182k
**Software Test Engineer - Medical Device Integration (Bedford, MA)** You will join a high-performing software team in Philips Image Guided Therapy... ...are complete, clear, and testable. Supports high-quality delivery by validating requirements readiness.* Develops and...SuggestedFull timeWork at officeImmediate startWork visaRelocation package3 days per week$115k - $182k
Software Test Engineer - Medical Device Integration (Bedford, MA) Job Description You will join a high‑performing software team in Philips Image... ...requirements are complete, clear, and testable. Support high‑quality delivery by validating requirements readiness. Develop and...SuggestedFull timeWork at officeWork visaRelocation package3 days per week- ...Group, Inc. is seeking a Manufacturing Engineer I in Wilmington, Massachusetts. The role... ...tailored implants. Responsibilities include assuring compliance with regulations, optimizing... ...1-3 years of experience in the medical device industry, excellent communication skills...
$90k - $115k
Anika is seeking a Validation Engineer II based in Bedford, MA, responsible for managing validation processes for pharmaceutical and medical device manufacturing. The ideal candidate has 3-5 years of validation experience and a strong understanding of cGMP regulations....Full time$10k
Software Quality Assurance Engineer II/III (341851) Job Summary You will have the opportunity to work in a multi-functional team environment with a wide diversity of exciting technologies and products. Whether your desired career path is technical or leadership, Textron...Temporary workCasual workWork at officeFlexible hours$160k - $180k
...will oversee full testing processes and ensure high standards of quality in compliance with applicable regulations. The ideal candidate... ...of product development experience and a Bachelor's degree in Engineering or Science. This position offers competitive compensation in...$115k - $182k
Philips Iberica SAU is seeking a Software Test Engineer in Bedford, MA, to join a high-performing team focused on verifying software solutions in the cardiovascular diagnostic space. You will collaborate closely with other teams, ensuring the software meets all functional...3 days per week- Philips International is seeking a Software Test Engineer for their Bedford, MA location. In this role, you will validate software solutions in the cardiovascular diagnostic space to ensure they meet functional, safety, and performance standards. We're looking for a candidate...Full timeWork at office
- ConforMIS, Inc. is seeking a Product Quality Engineer II in Wilmington, Massachusetts. This role involves quality assurance activities including product quality engineering, non... ...least 2 years of experience in the medical device industry, a Bachelor's degree in a related...
- Analog Devices, Inc. is seeking a Quality Systems Engineer in Wilmington, MA to develop and maintain quality management systems for medical devices. Responsibilities include supporting compliance with ISO 13485 and FDA regulations, coordinating training activities, and...
$102.48k - $163.97k
Mass Digital Health is looking for a Software Design Quality Engineer located in Bedford, MA. You will be responsible for developing and managing comprehensive software quality documentation, ensuring regulatory compliance throughout the software lifecycle. The ideal candidate...Full time$130k - $160k
...Overview Position Summary: The Senior Software Quality Engineer position is responsible to ensure that activities throughout the product lifecycle... .... Experience: A minimum of 8 years of experience in medical devices, pharmaceuticals, diagnostic industry, or clinical laboratory...Work experience placement- 1010 Analog Devices Inc. is seeking a motivated Quality Systems Engineer to support the development and maintenance of quality management systems for medical devices, ensuring compliance with ISO 13485 and FDA regulations. The role includes responsibilities as a Training...
- Job Title: Devie - Senior Quality Engineer, Invitro Diagnostics Location: Cambridge, MA About the Job The Senior Quality Engineer - IVD Devices is a senior subject matter expert responsible for ensuring the quality, safety, and regulatory compliance of IVD devices across...
$90k - $130k
Job Title Device Quality Engineer - Device Risk Management and Surveillance Excellence Location Cambridge, MA About the Job The Device Quality Engineer leads global processes for patient safety and regulatory compliance. The role maintains and continuously improves Device...$160k - $180k
Overview Position Summary: Using Engineering procedures standard for research and development... ..., automation scripts, and test code for quality and accuracy Assess existing test... ...design controls and applicable medical device regulations and standards (e.g., ISO 134...$102.48k - $163.97k
...Job TitleSoftware Design Quality EngineerJob DescriptionThe Software Design Quality Engineer is responsible for developing, maintaining... ...pre- and post-market medical device software.Conducts detailed... ...a focus on Software Design Assurance/Control, detailed knowledge of...Full timeWork at officeImmediate startWork visaRelocation package3 days per week- ...was awarded the first X-Prize to be given for healthcare. The Compliance Engineer is responsible for the organization and the coordination of processes pertaining to regulatory compliance and quality systems to ensure regulatory requirements for compliance DUTIES...
$90k - $130k
Sanofi is seeking a Device Quality Engineer to enhance patient safety and ensure compliance with regulations in Cambridge, MA. The ideal candidate will lead the Device Risk Management processes and collaborate cross-functionally to ensure product safety. Responsibilities...$90k - $120k
We are seeking an Engineer III to support systems engineering programs related to software within a medical device environment. This individual will execute technical workstreams, partnering with various teams to troubleshoot complex issues. The successful candidate will...$90k - $120k
Werfenlife SA. is seeking an Engineer III to support systems engineering programs in a regulated medical device setting. This role emphasizes hands-on contributions to software-related investigations and complex problem troubleshooting, engaging collaboratively across...$69.75k - $93k
Philips Iberica SAU seeks a Product Industrialization Test Engineer for developing and optimizing manufacturing processes in a regulated medical device setting. This role involves supporting the transition from design to manufacturing, managing Bills of Materials, and...- Amgen SA in Cambridge, MA, seeks an Engineer I for laboratory testing and operations. In this role, you’ll join a high-performing team... ...biopharmaceutical company, performing laboratory work including drug delivery device testing and maintaining lab compliance. The position requires a...
$90k - $120k
Werfen is seeking an Engineer III to contribute to systems engineering programs in a regulated medical device environment. This role involves troubleshooting software and systems issues, leading investigations, and supporting cross-functional teams. Ideal candidates will...$102.48k - $163.97k
Software Design Quality Engineer Job Description Software Design Quality Engineer responsible for... ...for pre‑ and post‑market medical device software. Conduct detailed root cause... ...environments, with a focus on Software Design Assurance/Control, detailed knowledge of Risk...Full timeWork at officeWork visaRelocation package3 days per week$110k - $140k
...supervision, as a member of the R&D Software Engineering team at Werfen, this role focuses on... ...and timely solutions. Produce high-quality technical documentation to support compliance... ...functions within application and with devices Evaluates, investigates, and implements...- Philips International in Cambridge, Massachusetts is seeking a Service & Delivery Quality Process Engineer. This role emphasizes quality management in medical devices, requiring a bachelor's degree and over 5 years of experience in Q&R roles. The successful candidate will...
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