Engineering jobs in Manchester, New Hampshire - Page 2Crear alertas

Job DescriptionDEKA Research and Development, housed in Manchester, NH, has an exciting opportunity for an Electrical Engineering Intern to work in a dynamic Research and Development environment. In this role you will work alongside a group of passionate engineers to create innovative solutions that truly make a difference. DEKA offers Internships and Co-Ops for full time students* (must be at least 18 years of age). Internships last a minimum of 10 weeks, but 12 weeks is preferred. All summer internships must start no later than June 15, 2026. How you will make an impact as an Electrical Engineering Intern: • Support the development of new products and new product concepts, • Perform characterization of electrical circuits and document performance, • Assist in failure analysis • Perform verification and validation activities using test equipment and test fixtures, • Troubleshoot electromechanical prototypes, • Use electrical CAD tools for schematic capture and PCB layout (Altium), • Must be currently enrolled in an undergraduate or graduate Electrical Engineering program, • Knowledge of analog circuits (signal and low-power) • Knowledge of digital electronics, • Must have exposure to electrical CAD tools (schematic and layout), • Firmware programming experience on Arduino or similar is a plus., • Must have excellent verbal and written communication skills, • Must be a self-starter eager to contribute in a team environment Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored. Additional Information: *Applicants should be aware that short-term housing options in Manchester, NH are limited and that DEKA is not able to assist with housing. Public transportation is available and routes/schedules can be found by visiting the Manchester Transit Authority website, . Please be aware that we try to make sure that our internship opportunities are well defined and will provide a unique experience. We understand that most candidates would like to know if they have a placement as soon as possible, but at DEKA it takes more time than other companies at we review every application that is submitted. We will try to let you know as soon as we can, but encourage you to pursue other opportunities as well. *A full time student is defined as being enrolled in a minimum of 12 credits per semester at an undergraduate program, or a minimum of 9 credits per semester for a graduate program. Powered by JazzHR i5ktZNypcY

Job DescriptionDescription: As an Entry Level Civil Engineer in the Aviation Services Group, you will provide a broad range of assistance and support to Project Managers, Planners, and Construction Managers. The position can be based out of any of our New England offices (Burlington, VT, Chelmsford, MA, Manchester, NH, Portsmouth, NH or Yarmouth, ME). Hoyle Tanner has earned the reputation as experts across a wide array of specialties and our greatest strength lies in the passion, talent, and uniqueness of each of our team members. This is your opportunity to join the great team at Hoyle, Tanner & Associates, Inc. You will: • Work on airport infrastructure and civil engineering projects with an assigned team, • Complete assignments with direction from the Project Engineer or Project Manager, • Perform design calculations and related tasks, • Preparing technical specifications and reports, • Ensuring compliance with applicable design, safety or environmental regulations, • Work as part of an integrated, multi-discipline team to solve technical challenges, • Use software and other tools to develop designs and organize work, • Gather, research and maintain engineering data records including tests, drawings, and field data, • May attend site visits and meetings with clients and contractors, • May be responsible for construction observation and limited administration, • May participate in professional training with direction from the Project Engineer or Project Manager, • Read and understand technical drawings and specifications, • Demonstrate strong writing and communication skillsRequirements:, • BS in Civil Engineering (Masters preferred) or Construction Management, • EIT is preferred, or ability to obtain, • 0-2 years of experience

Job DescriptionDescription: Hoyle Tanner has an opportunity for an individual with 10-15 years of experience as a Senior Project Manager in our Ground Transportation Division. This senior position allows you to be involved in the leadership of the projects from start-to-finish, mentor, work on potential pursuits of additional projects, develop project plans, schedules, and budgets. This position could lead to a business development position while utilizing your technical aptitude. Location: Manchester’s historic mill yard, our 30,000 square foot office space sits perched on the 5th floor of the original Amory Mill and is the home of our company’s headquarters. Remnants of the historic charm remain in various locations throughout the mill, while our space has been redesigned with modern lines and architectural accents. Job Responsibilities: • Hold the lead role in an integrated, multi-discipline team that solves technical project challenges of all types, • Understand project budget, scope of services, project schedule and project development, • Be a primary contributor or author of the development of technical and price proposals, • Monitor and review spent hours and dollars versus percent complete in relation to project timelines and budget and provide recommendations to the Project Manager to stay on track, • Understand the client’s organization and develop professional relationships with client peers, • Manage engineering staff and prioritize technical tasks to meet changes in schedule or resource availability, • Be proficient in technical writing, editing, and presentations, • Identify areas of improvement and regularly shares best practices and/or improve processes, • Develop person-hour estimates and budgets, • Act as a technical lead and demonstrate a specialized skill in a subject matter or application, • Potentially be the primary team member responsible for overall quality control of the project, • BSCE Degree required, MSCE preferred, • 10+ Years of relevant experience, • Current PE in NH, MA, ME, or VT, • Experience with the multiple engineering programs

Job DescriptionDEKA Research & Development, located in Manchester, NH, is seeking an Automation Machine Vision Engineer to join our industrial automation team developing vision inspection systems for medical device manufacturing. This role will collaborate with both our automation team and DEKA's robotic perception group to ensure product quality and manufacturing excellence. How you will make an impact as an Automation Machine Vision Engineer: • Design and maintain machine vision systems for detecting anomalies in manufactured medical devices including dimensional measurement, surface inspection, assembly verification, and seal integrity, • Select and specify cameras, lenses, and lighting configurations for diverse inspection challenges, • Integrate vision systems with Allen-Bradley PLCs and manufacturing automation equipment Apply both contrast-based and learning-based detection methods to solve inspection challenges, • Develop Python scripts and tools for data analysis and process improvement Support manufacturing sites and machine builders through regional travel (5-10%), • Advance vision capabilities through collaboration with DEKA's robotic perception groupTo be successful in this role, you will need the following skills:, • B.S. in Engineering, Computer Science, or equivalent work experience, • Remote and hybrid work not available, must be able to work on-site 5 days a week, • Minimum 3 years of hands-on experience with industrial machine vision systems, • Proficiency with Keyence vision systems (Cognex experience is a plus), • Strong understanding of optical component selection and lighting principles, • Python or other scripting language proficiency, • Experience integrating vision with PLCs and automation equipment, • Demonstrated ability to rapidly prototype and validate solutions under time-critical constraints, • Strong data-driven problem-solving and troubleshooting abilities, • Willingness to travel regionally (5-10%), • Clear technical documentation and communication skillsPreferred Qualifications:, • FDA-regulated medical device manufacturing experience, • Statistical process control, • Multiple vision platform experience, • Deep learning frameworks for vision applications One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age. Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored. Powered by JazzHR nzcthH4bOG

Job DescriptionDescription: Hoyle Tanner has an opportunity for an individual with 10-15 years of experience as a Senior Project Manager in our Ground Transportation Division. This senior position allows you to be involved in the leadership of the projects from start-to-finish, mentor, work on potential pursuits of additional projects, develop project plans, schedules, and budgets. This position could lead to a business development position while utilizing your technical aptitude. We are a welcoming, collaborative, respectful, encouraging, and diverse community where you can achieve your career goals. Our midsize allows you to be visible and heard. Hoyle Tanner offers you a flexible schedule, remote work opportunities and a generous sign-on bonus. See our impressive benefits package for more information. Location: Manchester, NH Manchester’s historic mill yard, our 30,000 square foot office space sits perched on the 5th floor of the original Amory Mill and is the home of our company’s headquarters. Remnants of the historic charm remain in various locations throughout the mill, while our space has been redesigned with modern lines and architectural accents. Job Responsibilities: • Lead and manage transportation engineering projects from inception to completion, • Develop project plans, schedules, and budgets, • Monitor and manage resources to complete projects in accordance with the contract, scope of services, budget, and schedule. Efficiently and effectively use Deltek and other management tools, • Lead and assemble a qualified project team to successfully complete complex projects or challenging client deliverables on time and within budget, • Provide superior client service by responding to needs and understanding concerns, • Provide technical expertise and guidance to team members, • Ensure compliance with all relevant regulations, standards, and guidelines, • Achieve excellent financial performance for Hoyle Tanner, • Maintain and foster team engagement and satisfaction in completing project tasks and collaborating with subconsultants and other disciplines, • Resolve team personnel conflicts in conjunction with supervisors, • Lead efforts in pursuit of potential projects and the development of technical and price proposals, • Promptly invoice for services rendered and advocate for outstanding accounts receivable, • Monitor product quality and ensure a quality management plan is developed with roles defined accordingly, • Keep Principal-In-Charge informed of potential claims or contract risks as they arise and collaborate on resolution strategies as needed, • Provide coaching, mentoring and feedback to other project managers Requirements: Qualifications • BS or MS degree (preferred), • PE License in one or more New England States, • 15+ years of increasing engineering or planning and leadership experience, • At least 5 years of experience as a project manager, • Strong communication skills, an acute understanding of project finances, scheduling, and client management skills

Job DescriptionWe are seeking a Manufacturing Engineer to drive process development, build execution, and the transition to scalable manufacturing for complex mechanical and electromechanical assemblies. This is a critical, cross-functional role that collaborates internally with engineering, supply chain, and operations teams, as well as externally with suppliers, partners, and customers. How You Will Make an Impact as a Manufacturing Engineer: • Develop and maintain essential manufacturing documentation including Bills of Materials (BOMs), line layouts, assembly instructions, fixtures, pFMEAs, and production control methods., • Plan, lead, and execute pre-production builds with a long-term vision for scalable, high-volume production., • Collaborate closely with design and engineering teams to ensure products are robust, reliable, and ready for manufacturing., • Consult with suppliers to define product specifications, and partner with the supply chain team to procure required equipment, materials, and parts., • Interface with manufacturing partners throughout the design transfer process to ensure on-time delivery of high-quality products that meet all performance criteria.Skills you will need to be successful in this role:, • B.S. in Mechanical or Manufacturing Engineering with 2–5 years of experience, or A.S. degree with 3–6 years of experience. Strong candidates with less experience may be considered., • Experience with electromechanical assembly and manufacturing process development., • Working knowledge of Lean Manufacturing, Six Sigma, or green manufacturing principles is a plus., • Proficiency in CAD software; SolidWorks preferred., • Familiarity with ERP systems is a plus., • Experience in medical device manufacturing is highly desirable., • Proven ability to set up manufacturing assembly lines with an eye toward scalability and efficiency., • Strong understanding of component forming processes, assembly operations, production line optimization, and design for manufacturability., • Demonstrated passion for solving complex engineering problems and a curiosity for understanding how things work. One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age. Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored. Powered by JazzHR jyY02Y6RJs

Job 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 Type Full-time Description GENTEX AT A GLANCE: At Gentex Corporation, we've created an environment where great ideas and great people can thrive. Leveraging a history that spans over 130 years, Gentex is a global leader in personal protection and situational awareness solutions for defense forces, emergency responders, and industrial personnel operating in high performance environments. Join our multinational team of exceptional and dedicated employees around the world and work on challenging and rewarding projects, grow your skills, and advance your career all while making a positive difference in the lives of our customers. Together, you and Gentex can build a career that's uniquely yours. MINIMUM QUALIFICATIONS: \n • B.S. Electrical Engineering, Computer Engineering or a related technical field\n The Manufacturing Engineer supports the development, improvement, and documentation of manufacturing processes within the Situational and Awareness Value Stream. This role applies technical skills to optimize and develop production processes, while also providing hands-on technical support and troubleshooting to manufacturing operations. Gentex offers a robust benefit package- including, but not limited to, medical coverages, 401k, paid time off and excellent work schedules including a 9/80 work week. RESPONSIBILITIES: • Troubleshoot and root-cause analysis of production electro-mechanical assemblies and subassemblies., • Participate in documenting and refining manufacturing processes to support production efficiency and quality standards., • Propose and provide input on new equipment design, development and procurement., • Contribute to the development and maintenance of work instructions, routers, and process documentation., • Support continuous improvement efforts using Lean principles with appropriate guidance., • Develop and enhance production tooling and equipment. Both custom-built and off-the-shelf solutions., • Collaborate with the production, engineering, and quality teams to troubleshoot basic problems in manufacturing operations and implement solutions., • Stay current with industry best practices, technology, and actively pursue opportunities for technical and professional growth. KNOWLEDGE, SKILLS AND ABILITIES: • Understanding of basic electro-mechanical systems; experience with projects in automation, electrical, or computer engineering disciplines is preferred., • Ability to apply data analysis tools (e.g., Excel, Minitab) to drive and verify process improvements., • Proficiency in engineering software tools such as MATLAB, LTspice, and Studio 5000/Connected Components Workbench (CCW) is a plus., • Skilled in the use of common hand tools, soldering irons, multimeters, oscilloscopes, power supplies, and other basic electronic test equipment; experienced with light fabrication tools for modifying or assembling fixtures and enclosures., • Exposure to parametric CAD software (e.g., SolidWorks) and Product Data Management (PDM) systems., • Exposure to ERP systems (e.g., SAP)., • Familiarity with basic quality standards, manufacturing documentation, and quality assurance protocols, including IQ, OQ, and PQ., • Strong analytical and problem-solving skills with excellent attention to detail., • Clear written and verbal communication skills; able to perform well in a team-oriented environment. TO APPLY: Visit: LOCATION: Gentex's Manchester facility is located in southern New Hampshire. Manchester is the largest convention, sports, entertainment, and arts & cultural destination in New Hampshire. There is so much to do, see and experience in Manchester including major concerts and ECHL Hockey, AA minor league baseball, live performances at the historic Palace Theatre or exhibits at our renowned museums. Located in the heart of New England, Manchester is also conveniently located within an hour's drive of Boston, an hour from the Atlantic Ocean and less than two hours from New Hampshire's scenic White Mountains, Lake Winnipesaukee and the many other well-known vacation destinations in Maine, Vermont and Massachusetts. Gentex Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard for any applicable state or federal protected class. Gentex is an E-Verify Participant. Pre-employment drug/alcohol/background screening is required.

Job Description InnoTECH Staffing has an immediate opening for a Sr. Quality Engineer to work in the Quality Department in a dynamic Medical Device Research and Development environment located in Manchester, NH. This requires being onsite 5 days a week and must be a US Citizen or Greencard holder. The position reports to the Director of Quality. We are seeking a Sr. Quality Engineer to provide Quality guidance in a dynamic, fast-paced medical device research, design assurance, manufacturing, and distribution environment. How you will make an impact as a Senior Quality Engineer: • Work cooperatively with cross functional design team members and project management to determine the best approach for on-going compliance with applicable SOPs and regulations, such as 21 CFR 820 and ISO 13485., • Use critical thinking to determine the best approach., • Use experience within Design Assurance or production and processing of medical devices to provide guidance and assistance in the development of new products., • Participate and lead in Risk Management activities in accordance with ISO 14971:2019., • The development, implementation, and approval of Hazard Analyses, FMEAs, and other Risk Analysis documentation., • Use experience with engineering and technology to identify and ensure compliance with applicable standards and regulations., • Lead investigations resulting in root cause and corrective actions through use of data analysis, inductive and deductive reasoning, and problem-solving skills., • Coordinate the efforts of individuals and teams performing investigations., • Use experience within manufacturing and monitoring of medical devices, to provide guidance in Root Cause Analysis and CAPA., • Ensure the accurate documentation and recording of information to be used in communication with partners and regulatory bodies., • Prepare detailed work plans such as Master Validation Plans., • Lead system and process improvements using six sigma tools., • Provide reliability and statistical analysis., • Conduct test method validations for formal testing., • Participate in internal and external audits., • Interface with partners on quality topics., • Evaluate and approve proposed design or manufacturing process change., • Drive system and process improvements., • Manage Suppliers and Supplier Qualifications per applicable Millyard supplier quality procedures., • Manage the Supplier Corrective and Preventive Action requests., • Facilitate the review and approval of supplier-initiated changes and communicate the approved changes to the appropriate departments. To be successful in this role, you will need the following skills & experience: • Bachelor’s degree in an engineering or related STEM discipline. Additional training and experience may be considered in lieu of degree., • Minimum 5 years' experience in any suitable occupation related to quality assurance of medical devices., • Experience with medical devices and direct responsibility for Risk Analysis and Design Transfer required., • Experience with compliance, applicable standards and regulations such as 21 CFR 820 and ISO 13485:2016 required., • Experience developing and leading quality system procedures required., • Experience supporting regulatory body submissions preferred., • Experience participating in internal and external audits preferred., • Hands-on experience in Supplier Qualification, Supplier Audits, and Supplier Corrective Action., • Ability to:, • Multitask and carry tasks through to completion., • Manage multiple sources of data and develop reports.

BETA Group, Inc is seeking a highly skilled and experienced senior bridge engineer ready to prove themself in a.This individual will have the opportunity to lead and oversee bridge/culvert design projects from initiation through completion.The ideal candidate should have previous experience piloting

Acts as Process Owner / Process Champion for assigned processes. The Manufacturing Process Engineer independently applies engineering theories and principles, managing moderately complex or contributing to complex projects in the design of process and support of products and tools in a manufacturing

The right candidate will have a degree in engineering or construction management, along with three years of experience in the overall direction, completion, and financial outcome of a construction project and/or the administrative activities, with self-perform experience. This individual will work c

Analyzes operational data and performance of wastewater treatment systems, and makes recommendations for troubleshooting process operations and process optimization. We are seeking an experienced Wastewater Process Engineer to join our team.

Proficiency in Python, security testing tools, and cloud security frameworks. Mentoring junior engineers, ML engineers, and security practitioners on AI security best practices. Working closely with cybersecurity, cloud engineering, MLOps, data engineering, and AI engineering teams, the engineer des

Acts as Process Owner / Process Champion for assigned processes. Manufacturing Process Engineers have a "Process Focus". The Manufacturing Process Engineer independently applies engineering theories and principles, managing moderately complex or contributing to complex projects in the design of proc

It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age. DEKA R&D has an immediate opening for a Product Complaints Engineer - Team Lead to work in a dynamic Medical Device Research and Development environment.

Technical experience in the development of processes and tools for products, manufacturing support, quality control, test equipment qualification and correlation, process, and gage capabilities. Use Failure Mode and Effects Analysis (FMEA) to assess and mitigate risk for critical processes, process

Coaches, reviews, and delegates work to lower-level professionals; Mentors lower-level engineers. Contributes to the foundational good of their domain and engineering overall, defining patterns and canonical examples, plus paying down tech debt.

DEKA Research & Development, located in Manchester, NH, is seeking an Automation Machine Vision Engineer to join our industrial automation team developing vision inspection systems for medical device manufacturing. It is now home to DEKA Research & Development, where we are taking the same innovatio

Proficiency in CAD software; SolidWorks preferred.

Quality Department in a dynamic Medical Device Research and Development environment. We are seeking a Quality Engineer to provide Quality guidance in a dynamic, fast-paced medical device research, development, and manufacturing and distribution environment. It is now home to DEKA Research and Develo

It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age. DEKA Research & Development, located in Manchester, NH, is seeking an Product Development Engineering Lead.

It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.

This individual will work closely with the owner, design, and construction team throughout the project lifecycle, and ideally will be a flexible, detail-oriented team player with expertise in architectural, civil, structural, and other commercial construction aspects, and a strong understanding of

Experience designing complex electro-mechanical assemblies in SolidWorks or other CAD system.

DEKA Research and Development, housed in Manchester, NH, has an exciting opportunity for an Electrical Engineering Intern to work in a dynamic Research and Development environment. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology in

It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age. We have an immediate opening for an EMC Test Engineer to work in a dynamic Medical Device Research and Development environment.

Computer Science, Computer Engineering, Software Engineering or equivalent program. DEKA Research and Development, housed in Manchester, NH, has an exciting opportunity for a Software Test Intern to join our software team and work in a dynamic R&D environment. This position will give exposure to sev

It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age.

DEKA Research and Development, housed in Manchester, NH, has an exciting opportunity for a Plastics Engineering Internto work in a dynamic R&D environment. Assist in part design reviews, material selection and general plastics research. It is now home to DEKA Research & Development, where we are tak

DEKA R&D has an immediate opening for a Product Complaints Engineer - Team Lead to work in a dynamic Medical Device Research and Development environment. It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age.

DEKA is looking for a hands-on, detail-oriented Engineering Service Technician to help keep our medical devices and test equipment running smoothly. Must have the ability to understand and follow established manufacturing Operating Procedures (OP) in the service process, and work within a Quality Ma

Job DescriptionJoin our dynamic team at DEKA and be at the forefront of driving quality excellence! As our Junior Quality Engineer, you'll be a key player in our collaborative environment, working hand-in-hand with cross-functional teams to ensure the highest standards of quality. Quality Engineering is a high-visibility role with a significant, direct impact on the success of the project. As a key contributor to our team, the following skills are required: • Aptitude for Learning Technical Information: Ability to comprehend and apply technical concepts effectively. Strong engineering foundation and technical skills., • Project Coordination/Management: Skilled in planning, executing, and managing projects with varying timelines., • Problem Solving: Embrace challenges and find creative solutions., • Collaboration: Effectively collaborate with various teams and departments, sharing ideas, taking initiative and proactively contribute to achieve common objectives. Work to maintain a positive attitude, fostering a supportive and productive work environment., • Attention to Detail: Display exceptional accuracy and precision in all tasks., • Effective Communication: Ability to articulate problems and solutions with clarity and precision to a diverse, cross-functional team with varying levels of technical aptitude, • Self-Motivated: Able to self-prioritize and work independently., • Technical Writing: Proficient in conveying complex technical information clearly and concisely to as variety of audiences., • Excellent at utilizing or the ability to quickly learn applications, including Excel, Word, and Visio.As a Jr. Quality Engineer, you will contribute in the following areas:, • Ensure an overall level of product quality in line with DEKA’s standards, • Support and participate in development of complex electromechanical devices, • Assist in the development, implementation and approval of Device Master Records and Device History Records, • Attain a comprehensive understanding of device design and core technologies, leveraging this knowledge to drive investigations and improvements in product design and process., • Participate in investigations resulting in root cause and corrective actions through use of data analysis, inductive and deductive reasoning, and problem solving skills, • Participate in Risk Management activities in accordance with ISO 14971:2019 such as FMEAs and Risk Analysis, • Use critical thinking and analysis to determine the best approach and provide guidance on QMS, FDA Part 820, and ISO 13485 compliance to design team members, • Review and approve quality records to ensure accuracy, completeness, and compliance with regulatory requirements.To be successful in this role as a Junior Quality Engineer, you will need the following skills:, • BS or MS degree in Biomedical, Mechanical, Electrical, or a related engineering/ Science discipline, • Ability to work as part of a multidisciplinary team, • Excellent verbal and written communication skills, as well as attention to detail, • Ability to understand and provide guidance on quality system procedures, • Project coordination/ management skills, • Technical Writing experience, • Excel, Word, Visio skillsNice skills to have:, • Knowledge of FDA’s Quality System Regulation, • Knowledge of ISO 13485 and related standards, • Experience with Corrective and Preventive Action (CAPA) One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age. Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored. Powered by JazzHR tFuyd4K5pE

Job DescriptionDEKA Research and Development, housed in Manchester, NH, has an exciting opportunity for a Software Test Intern to join our software team and work in a dynamic R&D environment. In this role you will work alongside a group of passionate engineers to create innovative solutions that truly make a difference. This position will give exposure to several different aspects of software test development including test automation, hands on trouble shooting, implementation of tests based on software requirements and working on a product that directly improves user’s lives. DEKA offers Internships and Co-Ops for full time students* (must be at least 18 years of age). Internships last a minimum of 10 weeks, 12 preferred. All summer internships must start no later than June 15, 2026. How you will make an impact as a Software Test Intern: • Write unit and automated tests for an Android app using Kotlin, • Write new software tools to facilitate testing, • Learn software processes, • Help review test and development code written by the teamTo be successful in this role as a Software Test Intern you need the following skills and experience:, • Must be currently enrolled as an undergraduate in a Computer Science, Computer Engineering, Software Engineering or equivalent program., • Kotlin, Java, or Python programming experience a plus, • Experience with Android development or testing and have successfully completed at least one year of programming course(s), • Must be a self-starter eager to contribute in a test team environment, • Must have excellent verbal and written communication skills One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age. Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored. Additional Information: *Applicants should be aware that short-term housing options in Manchester, NH are limited and that DEKA is not able to financially assist with housing. Public transportation is available and routes/schedules can be found by visiting the Manchester Transit Authority website, . Please be aware that we try to make sure that our internship opportunities are well defined and will provide a unique experience. We understand that most candidates would like to know if they have a placement as soon as possible, but at DEKA it takes more time than other companies at we review every application that is submitted. We will try to let you know as soon as we can, but encourage you to pursue other opportunities as well. *A full time student is defined as being enrolled in a minimum of 12 credits per semester at an undergraduate program, or a minimum of 9 credits per semester for a graduate program. Powered by JazzHR 2RMhgZJo7L

Job DescriptionBenefits/Perks • Competitive Compensation, • Great Work Environment, • Work with different departments to develop new products and processes, • Examine current manufacturing processes to see where improvements could be made, • Train and mentor new and existing employees on best manufacturing practices, • Troubleshoot problems with staff and suppliers, • Conduct audits internally and with suppliers to maintain high standardsQualifications, • Bachelor’s in Engineering or equivalent field, • Previous experience working in quality control desired, • Strong communication and organizational skills, • Excellent attention to detail, • Strong analytical skills

Job Description InnoTECH Staffing is looking to hire a Senior R&D Test Engineer for a product development company in Southern, New Hampshire. Ideal candidate should have medical device and/or pharma experience (Class II or III exp) This is onsite 5 days a week and candidate must be a US Citizen or Greencard Holder. Responsibilities: • Writing test plans, test procedures and other activities involving performance, durability, and reliability assessments, • Understanding of 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 or pharma 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

Job DescriptionDEKA R&D has an immediate opening for a Sr. Quality Engineer to work in the Quality Department in a dynamic Medical Device Research and Development environment. The position reports to the Director of Quality. We are seeking a Sr. Quality Engineer to provide Quality guidance in a dynamic, fast-paced medical device research, design assurance, manufacturing, and distribution environment. How you will make an impact: • Work cooperatively with cross functional design team members and project management to determine the best approach for on-going compliance with applicable SOPs and regulations, such as 21 CFR 820 and ISO 13485., • Use critical thinking to determine the best approach., • Use experience within Design Assurance or production and processing of medical devices to provide guidance and assistance in the development of new products., • Participate and lead in Risk Management activities in accordance with ISO 14971:2019., • The development, implementation, and approval of Hazard Analyses, FMEAs, and other Risk Analysis documentation., • Use experience with engineering and technology to identify and ensure compliance with applicable standards and regulations., • Lead investigations resulting in root cause and corrective actions through use of data analysis, inductive and deductive reasoning, and problem-solving skills., • Coordinate the efforts of individuals and teams performing investigations., • Use experience within manufacturing and monitoring of medical devices, to provide guidance in Root Cause Analysis and CAPA., • Ensure the accurate documentation and recording of information to be used in communication with partners and regulatory bodies., • Prepare detailed work plans such as Master Validation Plans., • Lead system and process improvements using six sigma tools., • Provide reliability and statistical analysis., • Conduct test method validations for formal testing., • Participate in internal and external audits., • Interface with partners on quality topics., • Evaluate and approve proposed design or manufacturing process change., • Drive system and process improvements.To be successful in this role, you will need the following skills and experience:, • Bachelor’s degree in industrial, mechanical or related engineering discipline required., • Minimum 5 years' experience in any suitable occupation related to quality assurance of medical devices., • Experience with medical devices and direct responsibility for Risk Analysis and Design Transfer required., • Experience with compliance, applicable standards and regulations such as 21 CFR 820 and ISO 13485:2016 required., • Experience developing and leading quality system procedures required., • Experience supporting regulatory body submissions preferred., • Experience participating in internal and external audits preferred., • Ability to:, • Multitask and carry tasks through to completion. Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored. Powered by JazzHR Me8boqDhwn

Job DescriptionDEKA R&D has an immediate opening for a Product Complaints Engineer to work in a dynamic Medical Device Research and Development environment. The position reports to the Product Complaints Manager. This is a high visibility role with a significant direct impact in the Quality Management System. How you will make an impact: • Responsible for reviewing complaints related to potential medical device issues., • Perform product complaint evaluations with minimal direction, utilizing experience and product knowledge., • Ensure that complaint documentation follows Good Documentation Practices; meets QMS requirements; and complies with U.S. Food and Drug Administration (FDA) regulations / other regulatory requirements., • Identify and make sound decisions regarding medical device reporting to regulatory agencies., • Interface with Third Party Manufacturers, health care professionals, internal customers, and regulatory agencies., • Participate in audits and CAPA investigations as they relate to complaint handling., • Work with the forensic investigation team to align product investigations related to complaints., • Generate reports to identify areas of process improvement., • Develop product training aids., • Contribute independently while also collaborating with other team members and departments needing product complaint information., • Maintain positive and cooperative communication with co-workers, customers, contractors, and vendors., • Serve as a subject matter expert on complaint handling., • Perform other related duties as assigned under management supervision.Skills needed to be successful:, • 4-year engineering degree, preferably in biomedical engineering; OR 2-year engineering degree and 2+ year(s) relevant experience in a cGMP environment supporting complaint handling investigations, medical device reporting, or product analysis., • Knowledge of FDA requirements for Quality Systems, pharmaceutical products, and Medical Device Reporting regulations (21 CFR 803, 820 and 211) is preferred., • Experience with SalesForce is preferred., • Strong motivation to see individual tasks through to completion, and to help as needed to achieve team goals., • Exceptional time management skills with the ability to prioritize multiple projects and ensure compliance with regulations and standard operating procedures., • Good problem-solving and proficient computer skills are required., • Solid written/verbal communication and organizational skills, as well as attention to detail., • Sound technical writing skills. FDseJooVXs

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