Medical Device Development Engineer - Regulatory - #1404326
Lynntech, Inc.
Date: 9 hours ago
City: College Station, TX
Contract type: Full time

Lynntech Is Seeking An Experienced Engineer With a Background In New Electromechanical Medical Device Development To Help Build Our Capability To Transition Technologies And Regulated Devices Into The Marketplace. The Engineer Will Be Involved In The Following Activities As Part Of a Team Of Technical And Regulatory Experts
Qualifications
Minimum qualifications include Master of Engineering or Master of Science in Biomedical Engineering, Mechanical Engineering, or related engineering disciplines, or bachelor's degree with at least 2 years of relevant work experience, as well as the following demonstrated strengths:
The ideal candidate will have a Master of Engineering or Master of Science degree in Biomedical Engineering, Mechanical Engineering, or related engineering disciplines with 3 or more years of experience, or bachelor's degree with 5 or more years of relevant work experience, as well as the following qualities and experiences:
Lynntech's mission is to solve real problems in defense, aerospace, medical, and energy markets by developing and commercializing innovative world-class technologies and products. To accomplish this mission, we need team members who are passionate about creating the latest in technology solutions, and who are driven to learn and grow.
Lynntech is built on a culture of collaboration - you will play an integral role within close-knit groups, working daily right alongside other talented engineers, scientists, and researchers. Throughout your career, you will have the opportunity to mature groundbreaking technologies into commercially viable solutions.
Long-term growth opportunities abound in Lynntech's engineering career path, where you determine your own ceiling according to your passion, proficiency, and ability to add value to the engineering team and the organization.
Some of the incredible variety of technology areas that Lynntech's engineers are involved in are:
Medical Devices
Lynntech is an EEO Employer.
- Defining indications for use and intended use
- Capturing user needs and developing design inputs
- Leading risk analyses and risk evaluations in accordance with ISO 14971
- Developing Safety Assurance Cases in accordance with FDA guidance
- Facilitating device design documentation and development processes in accordance with ISO 13485
- Reviewing draft test protocols
- Supporting regulatory strategy development for new devices
- Identifying potential predicate devices and reference devices
- Preparing design documentation in support of presubmission meetings with the FDA and other stakeholder meetings
- Supporting creation and maintenance of Design History File documentation
Qualifications
Minimum qualifications include Master of Engineering or Master of Science in Biomedical Engineering, Mechanical Engineering, or related engineering disciplines, or bachelor's degree with at least 2 years of relevant work experience, as well as the following demonstrated strengths:
- Phase II/III medical device development experience
- Class II medical device development experience
- Experience working for an established medical device manufacturer
- Experience working with straightforward regulatory pathways and FDA clearance (510(k))
- Familiarity with fluid mechanics, thermal management, material selection, machine design, controls, and manufacturing
- Proven skills in development of medical devices - contributing to requirements definition; risk analysis and evaluation; and prototype design, fabrication, assembly, and testing as a supporting member of a team
- Able to simultaneously consider functionality, performance, and risk while evaluating designs
- Creating, maintaining, and revising design documentation within a Quality System (ISO 13485)
The ideal candidate will have a Master of Engineering or Master of Science degree in Biomedical Engineering, Mechanical Engineering, or related engineering disciplines with 3 or more years of experience, or bachelor's degree with 5 or more years of relevant work experience, as well as the following qualities and experiences:
- Full medical product lifecycle experience from conceptualization through manufacturing, sustainment, and post-market monitoring
- Experience in a medical device startup or small business setting with new product development
- Developing devices with challenging regulatory requirements and nuanced regulatory pathways
- Developing disposable/single-use devices or components and associated durable systems
- Proven leadership skills in developing medical devices - leading requirements definition, leading risk analysis and evaluation, and interfacing directly with regulatory affairs personnel and the FDA
- Training new personnel on following design controls within a Quality System (ISO 13485)
- Familiar with standardized testing (g., IEC test standards, MIL-STD-810)
- Experience with Verification and Validation testing
- Developing and clearing disposable/single-use devices or components and associated durable equipment
- Leading Design Failure Mode and Effect Analyses (DFMEA)
Lynntech's mission is to solve real problems in defense, aerospace, medical, and energy markets by developing and commercializing innovative world-class technologies and products. To accomplish this mission, we need team members who are passionate about creating the latest in technology solutions, and who are driven to learn and grow.
Lynntech is built on a culture of collaboration - you will play an integral role within close-knit groups, working daily right alongside other talented engineers, scientists, and researchers. Throughout your career, you will have the opportunity to mature groundbreaking technologies into commercially viable solutions.
Long-term growth opportunities abound in Lynntech's engineering career path, where you determine your own ceiling according to your passion, proficiency, and ability to add value to the engineering team and the organization.
Some of the incredible variety of technology areas that Lynntech's engineers are involved in are:
Medical Devices
- Air platforms
- Space platforms
- Materials and Chemistry
- Biology and Life Science
- Human Systems
- Intelligent Systems
- Electronics
- Sensors
- Weapons
- Modeling
- Diagnostics
- Energy and Power
Lynntech is an EEO Employer.
How to apply
To apply for this job you need to authorize on our website. If you don't have an account yet, please register.
Post a resumeSimilar jobs
Restaurant Staff
MOD Pizza,
College Station, TX
1 day ago
MOD Restaurants make pizza to serve people, to contribute to a world that works for and includes everyone. We believe companies can and should be a force for good in the lives of the people they employ and the communities they serve. Because at MOD we don’t just make pizzas. We make pizzas that make the world a better place...

QC Chemist I
FUJIFILM Diosynth Biotechnologies,
College Station, TX
1 week ago
The work we do at FDB has never been more important—and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. Join FDB and help create the next vaccine, cure, or gene therapy...

Manufacturing Process Engineer I
FUJIFILM Diosynth Biotechnologies,
College Station, TX
3 weeks ago
Summary : The Manufacturing Process Engineer I is an integral part of the Manufacturing Technical Operations department located in College Station, Texas. This position will report directly to the Manager of Technical Operations, Manufacturing. Company Overview The work we do at FUJIFILM Diosynth Biotechnologies has never been more important—and we are looking for talented candidates to join us. We are...
