Job DescriptionJob Description InnoTECH Staffing has an immediate opening for a Test Engineer to work in a dynamic medical device R&D environment at our client who is located in Manchester, NH. This requires being onsite 5 days a week and must be a US Citizen or Greencard holder. Test Engineering is a high-visibility role with a significant, direct impact on the success of the project. How you will make an impact as a Verification and Validation Test Engineer: Developing and writing test procedures assessing end-to-end performance and reliability of user interfaces and hardware Understanding device design and core technologies in order to inform test method development Determining test coverage for revisions to design Creating and evaluating test fixtures if needed for product design verification Contributing to design failure investigations that may impact Risk Assessments, Hazard Analyses, and FMEAs Contributing toward regulatory and agency submissions Authoring Test Summaries and other documents To be successful in this role as a Verification and Validation Test Engineer, you will need the following skills and experience: Must have a BS in Physics, Biology, Electrical, Mechanical, or Biomedical Engineering. Experience with research, development, and product testing Experience writing procedures for others to follow Experience with data and failure analysis Broad measurement instrument knowledge Knowledge and deep understanding of engineering fundamentals Demonstrated problem solving ability and techniques Ability to work as part of an interdisciplinary team Self-motivated and able to self-prioritize Ability to clearly explain objectives Must be detail oriented and have excellent verbal and written communication skills Experience in medical devices, knowledge of FDA Quality System Regulations (QSRs) and/or ISO 13485, and other medical device industry experience preferred
04/24/2026
Full time
Job DescriptionJob Description InnoTECH Staffing has an immediate opening for a Test Engineer to work in a dynamic medical device R&D environment at our client who is located in Manchester, NH. This requires being onsite 5 days a week and must be a US Citizen or Greencard holder. Test Engineering is a high-visibility role with a significant, direct impact on the success of the project. How you will make an impact as a Verification and Validation Test Engineer: Developing and writing test procedures assessing end-to-end performance and reliability of user interfaces and hardware Understanding device design and core technologies in order to inform test method development Determining test coverage for revisions to design Creating and evaluating test fixtures if needed for product design verification Contributing to design failure investigations that may impact Risk Assessments, Hazard Analyses, and FMEAs Contributing toward regulatory and agency submissions Authoring Test Summaries and other documents To be successful in this role as a Verification and Validation Test Engineer, you will need the following skills and experience: Must have a BS in Physics, Biology, Electrical, Mechanical, or Biomedical Engineering. Experience with research, development, and product testing Experience writing procedures for others to follow Experience with data and failure analysis Broad measurement instrument knowledge Knowledge and deep understanding of engineering fundamentals Demonstrated problem solving ability and techniques Ability to work as part of an interdisciplinary team Self-motivated and able to self-prioritize Ability to clearly explain objectives Must be detail oriented and have excellent verbal and written communication skills Experience in medical devices, knowledge of FDA Quality System Regulations (QSRs) and/or ISO 13485, and other medical device industry experience preferred
Job DescriptionJob Description InnoTECH Staffing is looking to hire a Senior Test Engineer to work in a dynamic medical device R&D environment. This is a high visibility role with a direct impact on the success of our projects. It will be a great opportunity to work on some amazing projects that make a positive impact on the world. This requires being onsite 5 days a week in Manchester, NH. There is no sponsorship. How you will make an impact as a Senior Test Engineer: Writing test plans, test procedures and other activities involving performance, durability, and reliability assessments Understand device design and core technologies in order to inform test method development Determining test coverage for revisions to design Creating and evaluating test fixtures needed for product design verification Contributing to design failure investigations that may impact Risk Assessment, Hazard Analysis, and FTAs Participating and contributing toward regulatory and agency submissions Authoring Quality Plans, Test Summaries, and other documents What you need to be successful Senior Test Engineer: BS in Biomedical, Mechanical and/or Robotics/ Automation Engineering 3+ years' experience testing electro-mechanical devices (medical devices preferred) Must have laboratory/ wet lab skills and experience Must have fluid system handling experience Leadership and/or mentoring experience Knowledge and deep understanding of engineering fundamentals Capability to create and clearly explain team objectives and write procedures for others to follow Demonstrated problem solving ability and techniques Ability to work as part of an interdisciplinary team Self-motivated and able to self-prioritize Must have excellent verbal and written communication skills Preferred skills and experience: Knowledge of FDA Quality System Regulations (QSRs) and/or ISO 13485, and other medical device industry experience Experience with research, development, and product testing Experience writing procedures for others to follow Experience with data and failure analysis Broad measurement instrument knowledge
04/24/2026
Full time
Job DescriptionJob Description InnoTECH Staffing is looking to hire a Senior Test Engineer to work in a dynamic medical device R&D environment. This is a high visibility role with a direct impact on the success of our projects. It will be a great opportunity to work on some amazing projects that make a positive impact on the world. This requires being onsite 5 days a week in Manchester, NH. There is no sponsorship. How you will make an impact as a Senior Test Engineer: Writing test plans, test procedures and other activities involving performance, durability, and reliability assessments Understand device design and core technologies in order to inform test method development Determining test coverage for revisions to design Creating and evaluating test fixtures needed for product design verification Contributing to design failure investigations that may impact Risk Assessment, Hazard Analysis, and FTAs Participating and contributing toward regulatory and agency submissions Authoring Quality Plans, Test Summaries, and other documents What you need to be successful Senior Test Engineer: BS in Biomedical, Mechanical and/or Robotics/ Automation Engineering 3+ years' experience testing electro-mechanical devices (medical devices preferred) Must have laboratory/ wet lab skills and experience Must have fluid system handling experience Leadership and/or mentoring experience Knowledge and deep understanding of engineering fundamentals Capability to create and clearly explain team objectives and write procedures for others to follow Demonstrated problem solving ability and techniques Ability to work as part of an interdisciplinary team Self-motivated and able to self-prioritize Must have excellent verbal and written communication skills Preferred skills and experience: Knowledge of FDA Quality System Regulations (QSRs) and/or ISO 13485, and other medical device industry experience Experience with research, development, and product testing Experience writing procedures for others to follow Experience with data and failure analysis Broad measurement instrument knowledge
Job DescriptionJob Description InnoTECH Staffing is seeking a dynamic, results driven, and inventive Systems Engineer to assist in the development of a groundbreaking technologies. This is a great opportunity to roll up your sleeves and utilize your advanced engineering experience while playing a lead role for a life changing innovation. Systems engineers serve as technical guides and leaders to the project team as a whole. How you will make an impact as a Systems Engineer: Define the overall electro-mechanical system architecture, specifications, and design descriptions. Architect critical interfaces between software-driven subsystems to ensure flawless integration and function. Lead hazard and failure modes analysis (FMEA) to proactively identify and mitigate risks. Support the development of system-level test strategies, specifications, and protocols to ensure the product meets all performance and safety standards. Serve as a technical guide for your project team and collaborate with program management to drive design goals, including performance, cost, size, weight, and manufacturability. Provide expert guidance to manufacturing teams, contributing to process development through activities like PFMEA review. Support program management by estimating engineering effort and ensuring project plans align with technical goals. What you will need to succeed as a Systems Engineer: A BS or MS in an engineering discipline. A minimum of 2+ years of experience in the design of electro-mechanical products or machinery, with a proven track record of bringing new products from concept through commercialization. Demonstrates experience in a new product development environment, with knowledge spanning embedded software, complex mechanical systems, and electronics. Proven ability to define, manage, and test requirements for performance and standards compliance. Experience with testing and experimental methods, including the application of statistical techniques. Demonstrates technical leadership skills and a collaborative mindset to effectively guide and influence cross-functional teams. Must be detail oriented with strong written and verbal communication skills Depending on level and experience, salary is up to $150K. Requires being onsite 5 days a week in Manchester, NH Candidate must be a US Citizen or Greencard holder
04/24/2026
Full time
Job DescriptionJob Description InnoTECH Staffing is seeking a dynamic, results driven, and inventive Systems Engineer to assist in the development of a groundbreaking technologies. This is a great opportunity to roll up your sleeves and utilize your advanced engineering experience while playing a lead role for a life changing innovation. Systems engineers serve as technical guides and leaders to the project team as a whole. How you will make an impact as a Systems Engineer: Define the overall electro-mechanical system architecture, specifications, and design descriptions. Architect critical interfaces between software-driven subsystems to ensure flawless integration and function. Lead hazard and failure modes analysis (FMEA) to proactively identify and mitigate risks. Support the development of system-level test strategies, specifications, and protocols to ensure the product meets all performance and safety standards. Serve as a technical guide for your project team and collaborate with program management to drive design goals, including performance, cost, size, weight, and manufacturability. Provide expert guidance to manufacturing teams, contributing to process development through activities like PFMEA review. Support program management by estimating engineering effort and ensuring project plans align with technical goals. What you will need to succeed as a Systems Engineer: A BS or MS in an engineering discipline. A minimum of 2+ years of experience in the design of electro-mechanical products or machinery, with a proven track record of bringing new products from concept through commercialization. Demonstrates experience in a new product development environment, with knowledge spanning embedded software, complex mechanical systems, and electronics. Proven ability to define, manage, and test requirements for performance and standards compliance. Experience with testing and experimental methods, including the application of statistical techniques. Demonstrates technical leadership skills and a collaborative mindset to effectively guide and influence cross-functional teams. Must be detail oriented with strong written and verbal communication skills Depending on level and experience, salary is up to $150K. Requires being onsite 5 days a week in Manchester, NH Candidate must be a US Citizen or Greencard holder
Job DescriptionJob Description InnoTECH Staffing is seeking a Junior Control Systems Engineer in Manchester, NH. This is onsite 5 days a week. Must be a US Citizen or Greencard holder. In this role, you will contribute to the design and development of cutting-edge automation and robotics systems across two key domains: embedded medical devices and PLC-driven manufacturing automation. You will work alongside a multidisciplinary team of engineers to bring innovative prototypes from concept to reality. Responsibilities Embedded Medical Device Development Design and develop control systems for prototype medical devices running on embedded compute platforms Implement real-time control algorithms on embedded targets (e.g., ARM Cortex, FPGA, or DSP-based systems) Write and validate embedded firmware in C/C++ for safety-critical medical applications Collaborate with electrical and mechanical engineers to integrate sensors, actuators, and embedded hardware into functional prototypes Support design verification and validation (V&V) activities in compliance with medical device development standards. Create and maintain system requirements, software design documentation, and failure mode and effects analysis (FMEA) Manufacturing Automation Develop, program, and commission PLC-based automation systems for internal manufacturing equipment Integrate industrial sensors, drives, servo systems, and actuators into automation solutions Troubleshoot and optimize existing automation systems to improve reliability and throughput Collaborate with manufacturing engineers to translate process requirements into automated control solutions Document control system architectures, ladder logic, and functional specifications General Apply linear, non-linear, and optimal control techniques across both embedded and industrial platforms Develop and maintain control systems for automation and robotic products Support testing, debugging, and continuous improvement of prototype and production systems Required Qualifications B.S. in Mechanical, Electrical, Mechatronics, or Biomedical Engineering Foundational knowledge of linear and optimal controls theory Experience applying control algorithms in robotics or automation applications Proficiency in Python and C/C++ Familiarity with embedded systems concepts (real-time OS, hardware peripherals, firmware development) Experience with automation sensors, drives, and actuators Strong problem-solving, communication, and collaboration skills Preferred Qualifications PLC programming experience (Allen-Bradley, Siemens, or equivalent) Exposure to medical device development processes or regulated industries (FDA, ISO 13485, IEC 62304) Experience with real-time operating systems Familiarity with communication protocols used in embedded and industrial systems (CAN, SPI, I2C, EtherCAT, Modbus, PROFINET) Knowledge of design verification and validation (V&V) methodologies Familiarity with version control systems (Git) and engineering documentation practices
04/24/2026
Full time
Job DescriptionJob Description InnoTECH Staffing is seeking a Junior Control Systems Engineer in Manchester, NH. This is onsite 5 days a week. Must be a US Citizen or Greencard holder. In this role, you will contribute to the design and development of cutting-edge automation and robotics systems across two key domains: embedded medical devices and PLC-driven manufacturing automation. You will work alongside a multidisciplinary team of engineers to bring innovative prototypes from concept to reality. Responsibilities Embedded Medical Device Development Design and develop control systems for prototype medical devices running on embedded compute platforms Implement real-time control algorithms on embedded targets (e.g., ARM Cortex, FPGA, or DSP-based systems) Write and validate embedded firmware in C/C++ for safety-critical medical applications Collaborate with electrical and mechanical engineers to integrate sensors, actuators, and embedded hardware into functional prototypes Support design verification and validation (V&V) activities in compliance with medical device development standards. Create and maintain system requirements, software design documentation, and failure mode and effects analysis (FMEA) Manufacturing Automation Develop, program, and commission PLC-based automation systems for internal manufacturing equipment Integrate industrial sensors, drives, servo systems, and actuators into automation solutions Troubleshoot and optimize existing automation systems to improve reliability and throughput Collaborate with manufacturing engineers to translate process requirements into automated control solutions Document control system architectures, ladder logic, and functional specifications General Apply linear, non-linear, and optimal control techniques across both embedded and industrial platforms Develop and maintain control systems for automation and robotic products Support testing, debugging, and continuous improvement of prototype and production systems Required Qualifications B.S. in Mechanical, Electrical, Mechatronics, or Biomedical Engineering Foundational knowledge of linear and optimal controls theory Experience applying control algorithms in robotics or automation applications Proficiency in Python and C/C++ Familiarity with embedded systems concepts (real-time OS, hardware peripherals, firmware development) Experience with automation sensors, drives, and actuators Strong problem-solving, communication, and collaboration skills Preferred Qualifications PLC programming experience (Allen-Bradley, Siemens, or equivalent) Exposure to medical device development processes or regulated industries (FDA, ISO 13485, IEC 62304) Experience with real-time operating systems Familiarity with communication protocols used in embedded and industrial systems (CAN, SPI, I2C, EtherCAT, Modbus, PROFINET) Knowledge of design verification and validation (V&V) methodologies Familiarity with version control systems (Git) and engineering documentation practices