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Software/Hardware Quality Engineer

Intelon Optics, Inc. Hope ,RI
  • Posted: over a month ago
  • $90,000 to $110,000 Yearly
  • Full-Time
  • Benefits: medical, vision, dental
Job Description

Introduction

Intelon Optics is a rapidly-expanding world class medical technology and innovation company.

This position offers the opportunity to contribute to the Medical Technology business and help shape the future of intelligent medical devices for ophthalmology. If you are excited about solving complex, multivariate technical and systems challenges in the medical domain, are passionate about developing safe, robust and compliant high quality medical device that serves a meaningful purpose, and have excellent interpersonal and leadership skills, then this role could be for you. You will work with R&D team and lead the creation of innovative optical products and technologies. Your primary role would be to provide Software Quality Assurance testingand ensure compliance in the support of medical device development lifecycles.

In this fast-paced startup environment you will need excellent interpersonal skills, keen attention to detail, excellent communication/documentation, and ability to collaboratively and responsively, focusing on key priorities based on new information and product development timeline. You should have high energy and excitement to contribute to cutting-edge technology that improves medical care.

This role is based in our new state-of-the-art innovation center, located in Lexington, MA.

Responsibilities

• Perform and Review all test methods, design verification and validations on complex opto-electo-mechanical medical system with software controls. Work with R&D team to establish and document product requirements, test protocols and generate testreports.

• Create and maintain requirements tracematrix.

• Review Design and Development paperwork, records, etc. for compliance tointernal procedures and regulations. Participate in Phase/DesignReviews.

• Collaborate with engineers and SMEs to direct device risk management activities including UFMEA, DFMEA,PFMEA.

• Verify data integrity, electronic data storage and data sheetvalidations.

• Perform Data/Statistical analysis as needed. Support scientific, complaint, and test failure investigations.

• Providing support during internal and externalaudits

Requirements

BS in Engineering or related field and 4+ years or MS and 2+ year experience in medical device industry, particularly in medical equipment (software and hardware combination devices).

We are looking for someone who is adaptable, self-motivated, and able to work under pressure. We will expect you to be able to work collaboratively as part of a team and have the strong initiative and drive to work independently. You should have excellent interpersonal, communication, and presentation skills. Demonstrable track record of getting medical products through regulatory approvals is a significant plus.

Minimum Qualification

• Excellent communicationskills

• Strong understanding of Design Control process in Medical Device industry.

• A good understanding of the development principles applicable to regulatedproducts

• Technical training and experience using Statistics, Lean and Six Sigma Methodologies (i.e. including Measurement System Analysis, SPC, DOEs, Reliability,etc.)

• Knowledge of statistical software packages is preferred with the ability to preview, graphand analyzedata

Preferred Additional Qualifications

• Ability to read and understand technical documentation in a form of Visio diagrams, flowcharts, UML diagrams is aplus

• Knowledge and ability to use application control and performance evaluation tools (Services, Device Manager, Task manager,etc.)

• Attention to details, experience with instrument control software specifics

• Understanding and experience with Agile product development workflow andpractices

• Practical experience with JIRA required, other workflow / document collaboration tools (Confluence) is aplus

• Technical background in software or other engineering discipline

• Understanding US and International regulations and guidances for MedicalDevices

• Experience working with both an FDA and European regulatoryagencies

• Previous project management and/or project leadershipexperience

Benefits

Competitive salary and benefits with company incentive plan.

Diversity Statement

We believe that our company and business is better with a diverse team. We embrace and encourage our team members’ differences in age, ethnicity, disability, family or marital status, gender identity or expression, language, national origin, ability, political affiliation, race, religion, sexual orientation, socio-economic status, veteran status, and other characteristics that make our team members who they are.

Company Description
Medical Device Technology Company (www.intelon.com)

Intelon Optics, Inc.

Why Work Here?

We are a "can-do", diverse, and breakthrough medical device company committed to improving eye health around the world.

Medical Device Technology Company (www.intelon.com)

Address

91 Hartwell Avenue
Hope, RI
USA

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