Join Our Team

We offer exceptional opportunities for engineers and other innovators, competitive compensation and benefits, and an engaging and dynamic culture. Simbex is an equal opportunity employer.

Join Us

Like what you see? Do you have something to contribute to a collaborative environment where your engineering or software development expertise will be put to the test? Do you share our commitment to our core values of Passion, Integrity, Openness, Innovation, Agility, and Social Responsibility? Whether you are ready to build on your background in biomechanical systems, or have the tools and creative mind to help forge life-altering products, we want you to join our passionate team.

Some of the Benefits

  • Competitive Compensation
  • Medical and Dental Plans
  • Flexible Spending Account
  • Life Insurance
  • Retirement Savings Plan – 401K
  • Tuition Reimbursement and Professional Development
  • Paid Holidays and Generous Paid Time Off
  • Great Culture, Relaxed Environment in Beautiful New Hampshire
  • Paid Volunteer Time

Career Opportunities

Senior Systems Integration Engineer/Project Manager

Simbex seeks a dedicated Senior System Integration Engineer to serve as the technical lead for developing complex, electro-mechanical products for the consumer health and medical device markets.  This individual is responsible for all aspects of product life cycle management in the area of product development, from inception through engineering design and manufacture and works in concert with Simbex Project Managers to deliver novel product solutions within constraints of budget, schedule, and established quality processes and methodologies.  As a Functional Team member at Simbex (Electrical, Mechanical, or Software), the Senior Systems Integration Engineer will also be responsible for domain-specific architecture, design, and engineering of products.

Essential Functions:

  • Develops conceptual and detailed designs by analyzing product market requirements and performance requirements
  • Performs diverse and complex design, fabrication, modification, and evaluation of mechanical or electromechanical components, subsystems, and systems by applying engineering principles and developing new or unique analysis tools as required
  • Determines feasibility of designing new equipment or modifying existing equipment considering technical and economic factors, available resources, time constraints, and company planning by applying advanced analytical methods, creating design solutions, and establishing engineering plans
  • Provides technical information affecting long range product engineering planning by researching manufacturing or processing techniques, materials, properties, and process advantages and limitations
  • Recommends and implements process control specifications and related documentation.
  • Conducts complex analyses and devises tests pertaining to the development of new designs, methods, materials or processes and completes required documentation by applying advanced engineering principles and company standards, and generating detailed reports, procedures, or change proposals
  • Develops acceptance, engineering evaluation, development and qualification/certification test plans, procedures, and reports. Compiles and analyzes operation, test, and research data to establish performance standards for newly designed or modified equipment or product
  • Investigates pertinent design factors such as human factors and ergonomics, ease of manufacture, availability of materials and equipment, interchangeability, strength-weight efficiency, contractual specification requirements, cost-determining optimum solutions, and implementing recommendations
  • Prepares or directs preparation of product or system layout and detailed drawings, assembly drawings, and schematics by coordinating with designers, drafters, or other engineers, interpreting customer and functional requirements, or by using engineering computer-aided design tools and following industry and/or military drawing standards
  • Reviews drawings and layouts to ensure clarity, completeness, functionality, and conformity to standards, procedures, and specifications. Identifies design errors, omissions, and other deficiencies, and directs revisions and improvements to engineers or other designers
  • Ensures internal project documents are complete, current, and stored according to Simbex’s Quality Management System
  • Concisely and accurately communicates development progress and results to internal and external customers (both written and verbal)

Click here to see the full job description.

To apply, send a resume and cover letter to hr@simbex.com

Software Quality Assurance Engineer

Simbex seeks a Software Quality Engineer responsible for ensuring software quality within complex medical device products through the development and execution of software test plans by way of verification procedures based upon software and system specifications. Together with an agile team, the QA Engineer will develop and translate requirements into high quality, reliable and scalable technology and products. Our ideal candidate will have experience designing test plans, identifying, testing and filing bugs, and writing and creating automated tests, and will initially be 50% manual testing and 50% automation testing.

Essential Duties and Responsibilities:

  • Review product design documentation to ensure that requirements stated are correct, unambiguous, and verifiable.
  • Consult with product development to evaluate system interfaces, operational requirements, and performance requirements of overall system.
  • Define test methods and create test plans for new or updated software projects to determine if the software will perform accurately and reliably according to documented requirements as well as established standards under both normal and abnormal conditions.
  • Design, develop and implement automated testing and tooling solutions with a focus on project and application-based automated functional and regression testing.
  • Recommend design improvements or corrections to engineers throughout the development process.
  • Maintain effective communication with the engineers on project limitation, capability, performance requirement and hardware interface changes.
  • Execute test plans and create test reports to describe program evaluation, testing, and correction.
  • Monitor program performance after implementation to prevent reoccurrence of program operating problems and ensure efficiency of operation.
  • Conduct compatibility tests with vendor-provided programs.
  • Formulate and design software systems, using scientific analysis and mathematical models to predict and measure outcome and consequences of design.
  • Create test tools that facilitate data gathering and test method execution.
  • Support manufacturing by verifying fixture software or any software used during production.
  • Support clinical studies by validating data collection processes.
  • Participate in risk management meetings.

Click here to read the full job description. 

To apply, submit a resume and cover letter to  hr@simbex.com.

Quality Systems Coordinator

Simbex seeks a dedicated Quality Systems Coordinator responsible for the maintenance of, and improvements to, Simbex’ ISO13485 compliant Quality Management System (QMS). This position ensures that the QMS is being implemented according to established standard operating procedures and works with the product development teams to ensure products are being developed and manufactured under appropriate controls.

ESSENTIAL FUNCTIONS

  • Partner with the project managers to ensure product development adheres to established and documented best practices and standard operating procedures.
  • Oversee the development and maintenance of procedures and policies required for the QMS.
  • Provide introductory and ongoing training to all employees on the QMS.
  • Plan and execute internal quality audits of Simbex processes and procedures.
  • Plan and oversee external quality audits of vendors/suppliers if necessary.
  • Oversee customer and agency audits. Ensure that appropriate documentation is established throughout the product development lifecycle.
  • Lead the quarterly QMS review meeting and ensure quality objectives are established and met.
  • Ensures that all quality documentation meet appropriate documentation standards and follows good documentation practices.
  • Ensure that staff are appropriately qualified to perform special processes.
  • Ensure record retention and maintenance of all quality system documentation, including change orders, work orders, deviation requests, etc.
  • Implements and maintains the project quality plan on assigned projects, and ensures that customers execute documents as defined in the project specific quality plans.
  • Oversees the corrective action process and ensures that non-conformities are appropriately documented and follow-up activities are executed.
  • Assume lead role in assuring compliance to local/federal regulations are being followed.
  • Oversee equipment Calibration system and coordination of services with external vendor.

Click here to see the full job description.

To apply, send a resume and cover letter to: hr@simbex.com.

REST API Developer

Simbex seeks a dedicated REST API Developer, working as a member of a cross disciplinary team to provide the specification, design, development, and analysis of backend web services for the medical device and consumer health markets.  The REST API developer will provide technical guidance, follow sound software engineering principles, help guide design verification and validation, create and support unit/integration testing, and maintain code documentation.  The ideal candidate is a dependable and creative team player working with both software and electrical engineering cross-functional teams, and project teams.

Essential Functions:

  • Develop solutions that adhere to industry standard methodologies in areas such as design, performance, flexibility, user experience, and scalability while also ensuring the solution code-base is clean and well-documented with an emphasis on code quality, extensibility, security, reusability, and stability
  • Design, develop, and maintain highly secure, stable, scalable, and extensible solutions
  • Contribute to architectural design, automated testing, continuous integration and build management
  • Ensure quality through unit and functional test implementation and execution
  • Participate in and contribute to all phases of Product Development Life Cycle from Design Input to Design Verification and Test Automation
  • Develop and maintain code documentation including software development plans, architecture, software design, and requirements specifications
  • Analyze and influence technical, system, and/or user requirements. Identifies and creates solutions to improve system performance and availability. Facilitates root cause analysis of system issues to minimize impact and future occurrences
  • Assist project teams with software integration and coordination

Click here to see the full job description.

To apply, send a resume and cover letter to hr@simbex.com

Software Engineer

Simbex seeks a dedicated Software Engineer to support product development teams with software design, development, and testing for innovative products in the medical device and consumer health markets.  As a Software Engineer, you will assist with developing software across a range of platforms and devices from embedded to web following sound engineering principles and coding guidelines, maintaining code documentation, and executing software test plans.

Essential Functions:

  • Design / develop / test consumer facing software
  • Provide ongoing maintenance, support, and enhancements of existing software
  • Write clean, portable, scalable, documented, and sustainable code that conforms to industry based design patterns
  • Support the development of high-quality software design and architecture across multiple platforms and devices
  • Design, develop, implement and test software applications Create and maintain QA test automation and regression plans
  • Assist with the development and maintenance of software development operating procedures and tools/technologies to support software development
  • Maintain technical and user documentation within the Simbex Quality Management System
  • Work with third party design firms, hardware and software developer
  • Provide user and client support
  • Assist in the development and maintenance of data management functions in a data replication environment
  • Work as a member of the project team assigned to a specific development project
  • Ensure the quality and integrity of deliverables by adhering to FDA standards, guidelines, and process.
  • Perform other duties as required or requested

Click here to see the full job description.

To apply, send a resume and cover letter to: hr@simbex.com

Algorithm Development Engineer

Simbex seeks a dedicated Algorithm Development Engineer responsible for developing innovative and creative algorithms to extract meaningful and actionable insights from low cost wearable technologies/sensors in the consumer health and medical device space.  The Algorithm Development Engineer will be responsible for leading algorithm development throughout the product lifecycle – from defining requirements through design, development, testing, and deployment.  The successful candidate will have deep data analysis experience in time series/frequency analysis, sensor fusion, feature extraction, data reduction, classification techniques, optimization techniques, and machine learning.  This role requires a good deal of creativity and initiative that is applied to a diverse type of sensing technologies meeting the needs of both business and consumer stakeholders.

Click here to see the full job description.

To apply, send a resume and cover letter to: hr@simbex.com

Spring 2019 Product R&D Co-op

Simbex is a product development company focused on engineering human solutions. We bring to market medical innovations / technologies based upon personal biomechanical feedback; applying sensing technologies to facilitate rehabilitation, promote personal safety, and enhance performance training. Most of our engineering efforts fall into the electrical, mechanical, and software domains with a strong emphasis on integration and usability. Our Spring 2019 Product R&D Co-op will:

  • Assist with product design, manufacturing, and quality assurance tasks
  • Test prototype production equipment in laboratory and/or field settings
  • Prepare documentation to industry ISO 13485 standards
  • Complete an independent project with guidance from professional engineers

Requirements:

  • Be a sophomore or junior pursuing a Bachelor’s degree in Engineering (Mechanical, Electrical, Biomedical, or Computer Science)
  • Have experience using hand tools and performing mechanical or electrical testing,
  • Demonstrated problem solving capabilities and technical skills
  • Have a preferred minimum GPA of 3.0
  • Have a history of project work; it is highly recommended to describe past projects in your cover letter

Candidates interested in this January through June co-op should submit a resume and cover letter expressing interest to Kathy Karr, hr@simbex.com. Priority will be given to applications received by September 30. Please note that these are co-op positions (six months in duration). Anticipated pay is $16 hourly.

Spring 2019 Software/Web Developer Co-op

Simbex is a product development company focused on engineering human solutions. We bring to market medical innovations / technologies based upon personal biomechanical feedback; applying sensing technologies to facilitate rehabilitation, promote personal safety, and enhance performance training. Most of our engineering efforts fall into the electrical, mechanical, and software domains with a strong emphasis on integration and usability. Our Spring 2019 Co-op will:

  • Assist with product design, manufacturing, and quality assurance tasks
  • Prepare documentation to industry ISO 13485 standards
  • Complete an independent project with guidance from professional engineers
  • Assist with full-stack web development

Requirements:

  • Be a senior pursuing a Bachelor’s degree or a Master’s degree in Computer Science or related engineering discpline (Electrical Engineering, Computer Engineering, Software Engineering),
  • Demonstrated problem solving capabilities and technical skills
  • Demonstrative programming and web development skills
  • Have a preferred minimum GPA of 3.0
  • Have a history of project work; it is highly recommended to describe past projects in your cover letter
  • Experience performing mechanical or electrical testing desired

Candidates interested in this January through June co-op should submit a resume and cover letter expressing interest to Kathy Karr, hr@simbex.com. Priority will be given to applications received by September 30. Please note that these are co-op positions (six months in duration).

Entrepreneur Fellow (TREAT)

The TREAT Entrepreneur Fellowship Program is an immersive cooperative educational and professional opportunity for individuals seeking experience in technology translation and commercialization. TREAT, and its member organizations, developed a program to encourage the
rapid adoption of the core principals of commercialization to empower entrepreneurs with the resources and skill sets needed to bring their idea or device to market. The program amplifies the benefits delivered to entrepreneurs, researchers, and clinicians who participate in TREAT by aligning Commercialization Assistance Program clients with Entrepreneur Fellows. The combination of complementary skill sets and expertise will help projects overcome the many hurdles presented during the commercialization process.

Fellows will investigate and evaluate potential and existing TREAT projects on their methods, successes and failures via regular one-on-one meetings with their TREAT mentor. Fellows will join the TREAT leadership team and participate in regular meetings, including reviews, critiques,
and assistance to the broad spectrum of rehabilitation and assistive technology commercialization projects that make up TREAT’s clients.

Fellowship Activities:

  • Review, analyze, and provide feedback on TREAT Commercialization Assistance Abstracts and Proposals
  • Deliver strategic advisement, subject matter expertise, and project support to clients in the
  • Commercialization Assistance Program
  • Contribute to ongoing TREAT program development activities
  • Develop and execute product development strategies with commercialization experts

Benefits:

  • Immersive and experiential learning of the TREAT Commercialization Methodology
  • Mentorship and advisement from seasoned entrepreneurs and commercialization experts
  • Direct engagement with innovators and industry pioneers developing novel rehabilitation and assistive technologies
  • Learn how to navigate the regulatory, reimbursement, and intellectual property pathways for medical device development

Requirements:

  • Ideal candidates for a TREAT Fellowship position will be post-graduates or those seeking a post-graduate degree with an educational background in technology, business, clinical, or healthcare delivery and a strong interest in entrepreneurship and technology commercialization. Preference
    will be given to those candidates who are able to spend at least a portion of their Fellowship tenure at the TREAT offices in Lebanon, NH.
  • Fellowship candidates will be considered on a rolling basis with a desired appointment duration of 6-12 months.

For more information about TREAT visit: TREATcenter.org

To view the Entrepreneur Fellowship Overview and Application, please go here: TREAT Fellowship Application

Please note that the application must be submitted with the requested additional information for consideration. Questions and/or completed applications
may be directed to info@treatcenter.org

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