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Experience Level
Not Applicable
Qualifications
Ideal candidates will possess a strong background in engineering, particularly in automation and control systems. We are seeking individuals with excellent problem-solving skills and a keen attention to detail. Familiarity with medical device regulations and quality assurance protocols is preferred but not mandatory.
About the job
Join our innovative team at System Canada Technologies as a Medical Devices Automation Engineer. In this role, you will spearhead automation processes to enhance the efficiency and reliability of our medical device manufacturing. You will collaborate with cross-functional teams to develop and implement automation strategies, ensuring compliance with industry standards.
About System Canada Technologies
System Canada Technologies is at the forefront of medical device innovation, dedicated to enhancing healthcare through advanced technology. We pride ourselves on our commitment to quality and our collaborative work environment, fostering growth and development for all employees.
Join our innovative team at System Canada Technologies as a Medical Devices Automation Engineer. In this role, you will spearhead automation processes to enhance the efficiency and reliability of our medical device manufacturing. You will collaborate with cross-functional teams to develop and implement automation strategies, ensuring compliance with industry…
About Beacon Biosignals Beacon Biosignals is advancing precision medicine for brain health. The company’s at-home EEG platform supports clinical development of new therapeutics for neurological, psychiatric, and sleep disorders. Beacon’s FDA 510(k)-cleared Waveband EEG headband and proprietary AI algorithms enable quantitative biomarker discovery and application. With a Clinico-EEG database spanning nearly 100,000 patients, Beacon’s cloud-native analytics platform powers large-scale retrospective and predictive studies using real-world data. The team is working to redefine treatment for conditions affecting brain physiology. Role Overview: Director of Device Engineering The Director of Device Engineering leads a multidisciplinary team focused on hardware and systems engineering. Reporting to the VP of Device Engineering, this leader shapes and executes the device engineering strategy while overseeing daily operations and team development. Key Responsibilities Guide the full lifecycle of home sleep testing products, from concept and architecture through verification, regulatory submission, manufacturing transfer, commercialization, and ongoing support. Deliver safe, reliable, and high-quality medical devices that meet clinical needs, regulatory requirements, and business goals. Direct product support efforts, including vendor and contract manufacturer management, resolving production issues, improving yields, and implementing design changes to enhance reliability, performance, and scalability. Collaborate with Quality Assurance, Regulatory Affairs, Clinical Operations, and Logistics teams to uphold rigorous design controls, risk management, and audit readiness in line with medical device regulations. Maintain high standards for safety, compliance, system integrity, and product quality as the company grows. Location This position is based in the Boston area to support close collaboration with the local team.
Full-time|On-site|Boston, Massachusetts, United States
TransPerfect delivers language services and technology solutions to enterprise clients worldwide. With operations in more than 100 cities and support for over 170 languages, the company helps organizations manage multilingual content efficiently through its GlobalLink® platform. TransPerfect holds ISO 9001 and ISO 17100 certifications. Headquarters are in New York, with additional offices in London and Hong Kong. More information is available at www.transperfect.com. Role overview The Account Executive for the medical device sector develops new business and supports existing clients in the Boston area. This role expands TransPerfect’s presence and strengthens partnerships within the medical device industry. What you will do Drive business development in the region to create new revenue opportunities. Identify and reach out to potential clients through online research, trade shows, referrals, and professional networks. Engage new clients using cold calling, networking, and participation in industry events. Design and implement sales strategies to meet monthly, quarterly, and annual targets. Present TransPerfect’s solutions in both virtual and in-person meetings, adapting to client needs. Refine business development tactics specific to the medical device market. Negotiate pricing and project timelines with new and existing clients. Explain the translation process, pricing, turnaround times, and how TransPerfect compares with competitors. Develop account strategies at regional and national levels to achieve revenue and margin goals. Build a strong understanding of TransPerfect’s services and their value in the market. Deepen relationships with key customers and broaden engagement across accounts. Location Boston, Massachusetts, United States
The Account Executive, Medical Devices and Life Sciences role at InterSystems focuses on driving growth in these sectors from the Boston office. The position centers on building strong relationships with both new prospects and existing customers, supporting the expansion of the HealthShare platform. HealthShare connects patient data and enables interoperability and analytics for healthcare organizations. Key responsibilities Promote InterSystems products and services to organizations in the medical devices and life sciences fields, prioritizing new business development. Create and implement sales strategies to increase revenue within assigned accounts. Act as the main contact for customer organizations, strengthening connections at various levels. Work closely with internal teams to meet sales goals and deliver value to clients. Collect and communicate customer feedback on products to support ongoing improvements. Grow new business revenue while maintaining and expanding relationships with current customers. Location This position is based in Boston, MA.
About Hike MedicalHike Medical is revolutionizing musculoskeletal care, beginning with foot health. Our innovative AI-driven vision platform transforms a quick 30-second web-based foot scan into custom-engineered, 3D-printed insoles that help prevent pain before it occurs. We are already safeguarding the well-being of on-their-feet workforces at Fortune 50 companies, significant health systems, and manufacturers across middle America. Recently funded by top-tier venture capitalists, we maintain a fast-paced, no-nonsense execution culture from our Boston Seaport headquarters as we aim for $100M ARR and to support 10 million Americans in their daily lives.First and only PDAC-approved 3D printed custom insole globally Three proprietary AI models enhancing the user experienceTwo product lines: one for employers & health plans, and another for clinics to provide affordable foot care, creating a beneficial cycle of clinician-validated data.Expanded access to care for over 100,000 Americans to dateRevenue growth of 10x from 2023 to 2024, with projections to continue this trend in 2025. Consistently profitable month-over-month.The RoleAs a Senior Software Engineer, you will develop and deploy the essential systems behind Hike’s AI healthcare platform. Serving as the backbone of Hike's rapidly growing, mission-driven initiative, you will design scalable services, implement production-ready AI, and create user experiences that enhance patient outcomes. From your first day, you will enjoy significant autonomy and a direct impact on transforming the US healthcare landscape.Why This Opportunity is Career-Defining:Your code will empower individuals to move without pain.You will have complete autonomy to create, deploy, and witness the outcomes—transitioning from concept to production in mere hours or days.You’ll collaborate with a high-performing team of elite engineers and AI researchers, where every addition substantially influences our mission.You'll thrive in a culture that rejects bureaucracy, discourages unnecessary complexity, and values trust as our core principle.What You'll Work On:Architect, build, and refine high-performance, scalable systems that drive AI-based solutions.Design resilient, serverless architectures within a TypeScript and AWS environment.Create developer-friendly APIs and SDKs to enhance integration and usability.
About SimpliSafe At SimpliSafe, we are an innovative home security company dedicated to safeguarding the life you've built. Our mission is to ensure that Every Home is Secure. We foster a culture that values your professional growth as much as our commitment to our customers. With an ego-free environment that encourages collaboration and innovation, we welcome individuals who are passionate about making a significant impact in the home security industry. We don’t just want you to work here; we want you to flourish and succeed. We embrace a hybrid work model, allowing our teams to balance their time between the office and home. Our hybrid approach typically requires in-person collaboration on two core days, often Tuesday, Wednesday, or Thursday, while providing the flexibility to work remotely the rest of the week. This model enables us to leverage the best of both worlds for our productivity. Why Join Us? As we continue to grow, we seek talented, intelligent, and humble individuals who align with our values and are eager to join us in revolutionizing the home security landscape while pursuing our mission of keeping Every Home Secure. Your Role You will be part of SimpliSafe’s Device Cloud Services team, striving to enhance cloud-based systems that allow customers to manage their home security from anywhere globally. We are in search of a driven and experienced Senior Software Engineer to architect, develop, maintain, and take ownership of software solutions. As a backend team, we tackle large-scale distributed challenges, ensuring our customers enjoy real-time access and control over their security systems. Our core principles revolve around life safety, reliability, simplicity, and performance. Key Responsibilities: Design and develop robust solutions, mentoring junior engineers to grasp product requirements and create scalable, reliable systems. Implement and maintain tests to ensure high-level functionality and safe refactoring of solutions. Engage in long-term support and maintenance tasks, including performance optimization, bug fixes, feature enhancements, design improvements, and automation. Document the systems you develop to facilitate future maintenance and upgrades by subsequent developers. Act as an on-call first responder for software under your team's purview.
Full-time|$141K/yr - $225.6K/yr|Hybrid|Boston, Massachusetts, United States
Join Axon and be a Force for Good.At Axon, our mission is to Protect Life. We are pioneers tackling some of society's most pressing safety and justice challenges through our innovative ecosystem of devices and cloud software. We thrive on collaboration, fostering open communication and valuing diverse perspectives from our customers, communities, and each other.Life at Axon is dynamic, rewarding, and impactful. Here, you’ll take ownership and effect real change, growing constantly as you contribute to a mission that truly matters at a company that values you. Your ImpactAs a member of our high-performing software engineering team, you will develop embedded software for Axon’s devices, ensuring critical evidence is captured during vital moments for our customers. This role offers the chance to collaborate with talented software and firmware engineers and to contribute to the development of next-generation public safety products, including body-worn cameras, in-car cameras, and wireless microphones.Your role requires you to engage deeply in architectural decisions that will influence our products. You are committed to crafting device software characterized by high stability and rapid, consistent performance. With a passion for working with cutting-edge open-source technologies, you will leverage your systems design expertise to make sound technical decisions for robust systems.In addition to driving decisions among competing engineering trade-offs, your empathy for customers will enable you to propose innovative solutions to their challenges. You will work closely with product managers and designers to ensure we are developing the right solutions for our customers. Furthermore, you enjoy mentoring fellow engineers, acting as a hands-on teacher to elevate the team around you.As an Embedded Application Software Engineer, your responsibilities will include designing, developing, testing, and maintaining embedded applications and networking configurations, along with the necessary systems and libraries, while interfacing with cloud and firmware services for the devices. Join our mission-driven team eager to positively impact the lives of first responders and those they serve.
Full-time|Hybrid|Boston, Massachusetts, United States
Job Title: Senior Sustaining EngineerLocation: Boston, MAEmployment Type: Full-time (Hybrid) About Activ SurgicalActiv Surgical is a pioneering medical device startup dedicated to revolutionizing surgical advanced visualization through innovative imaging, computer vision, and artificial intelligence technologies. Our platform seamlessly integrates state-of-the-art solutions to elevate laparoscopic and minimally invasive surgical procedures. Position OverviewAs a Senior Sustaining Engineer, you will take charge of the manufacturing processes, sustaining efforts, and continuous improvements for the Activ Surgical platform. Acting as the primary technical liaison with our contract manufacturer, you will facilitate cross-departmental collaboration across Quality, Regulatory, Operations, and R&D teams. This role blends hands-on engineering expertise with structured problem-solving and detailed documentation in a dynamic startup environment.Your duties will encompass sustaining engineering, investigating hardware issues, implementing design-for-manufacture strategies, and managing the product development cycle for our existing platform. You will collaborate closely with Quality and Regulatory teams on handling complaints, non-conformance reports (NCRs), corrective and preventive actions (CAPAs), and field investigations, ensuring the device adheres to reliability, manufacturability, and compliance standards. Key ResponsibilitiesManufacturing Leadership & Technical InterfaceAct as the primary technical contact for the contract manufacturer, assisting with daily production, troubleshooting, and ensuring build readiness.Lead the resolution of manufacturing challenges, including assembly difficulties, test failures, yield enhancements, and line-down incidents.Review, approve, and contribute to updates in manufacturing documentation, including work instructions, testing procedures, and assembly processes.Drive the implementation of engineering change orders (ECOs) while ensuring compliant and controlled distribution at the contract manufacturer.Support manufacturing preparedness for engineering builds, pilot runs, and ongoing production.Sustaining Engineering & Quality InvestigationsLead root-cause analysis and corrective action initiatives for hardware-related issues, including complaints, NCRs, CAPAs, and field returns.Collaborate with Quality and Regulatory teams to ensure investigations and enhancements comply with ISO 13485 and FDA Quality System Regulations (QSR).Oversee sustaining engineering tasks to bolster reliability, robustness, and performance of the current hardware platform.Maintain hardware documentation and facilitate updates to risk management, verification, and traceability as necessary.Design for Manufacture & Process EnhancementsChampion design for manufacture (DFM), design for assembly (DFA), and process improvement initiatives aimed at increasing manufacturability, reducing costs, and optimizing assembly/testing workflows.
Full-time|$70K/yr - $73K/yr|Hybrid|Boston, Massachusetts, United States
Role Summary Responsibilities: Engage in projects that demand thorough analysis and presentation of clinical data, crucial for the successful adoption of innovative therapies. Salary: $70,000 to $73,000 per annum based on prior experience (this is a standardized, non-negotiable salary). Benefits: Enjoy hybrid working arrangements allowing up to 50% remote work, generous vacation allowance, flexible hours, private medical and dental coverage, 401K plan, life insurance, full funding for external training, comprehensive travel insurance, and more. Role Type: Full-time, permanent. Start Date: We are currently recruiting for positions starting in 2026. Location: This opportunity is based in our Boston office. About the RoleThe Analyst and Medical Writer roles are perfect for recent science graduates or those with scientific research experience, eager to apply their knowledge to impactful projects. These professionals will analyze clinical trial data and creatively present findings through various formats such as posters, slide sets, value dossiers, reports, and peer-reviewed publications. These deliverables play a vital role in our clients' communications with external stakeholders, facilitating the successful adoption of novel therapies. Work is organized on a project basis, involving three to four concurrent projects across a range of prominent disease areas and products, offering a diverse work experience and opportunities to develop a broad skill set.Collaboration is key, as you will work closely with seasoned colleagues who will provide training in both technical aspects and project management, as well as effective client communication. Your role will involve direct engagement with clients, with opportunities for teleconferences and in-person meetings, which may include travel within the US and internationally.Located in our Boston office, established in 2020, this role offers the chance to shape and influence our US operations, building on the success of our established presence in the UK and Asia. You will closely collaborate with our Scientific Director based in Boston.
Internship|$24/hr - $30/hr|On-site|Boston, Massachusetts, United States
Role OverviewKey Responsibilities: Engage in hands-on projects across Medical Communications, Evidence Development, and Value and Access domains, focusing on the assimilation, interpretation, and innovative presentation of scientific data related to pharmaceuticals and medical devices.Compensation: Competitive hourly wage ranging from $24 to $30, contingent on experience.Benefits: Enjoy a generous vacation leave policy, flexible working hours, the option to work from home one day per week, comprehensive medical, dental, and vision insurance, plus opportunities for social activities funded by the company.Role Type: Full-time, 3-month internship.Start Date: We are currently seeking candidates for Summer 2026; please indicate your availability on your application.Location: This position is based in our Boston office.About the InternshipThis Analyst/Medical Writer Internship is tailored for current students and recent graduates from scientific backgrounds looking to gain valuable insights into the operations of a premier healthcare consultancy. Interns will contribute to two to three distinct projects, involving tasks such as:Creating medical education presentationsConducting systematic literature reviewsDrafting clinical trial manuscriptsCompiling clinical and cost-effectiveness evidence to support HTA submissions to NICEThese impactful projects play a vital role in enhancing global healthcare outcomes. Interns will receive personalized training on the technical aspects of their roles and gain insights into project management and effective client communication.
Join SimpliSafe, a leader in home security technology, as a Senior Firmware Automation Engineer. In this pivotal role, you will be responsible for developing, implementing, and optimizing automated testing frameworks to ensure the highest quality of our firmware products. You will collaborate with cross-functional teams to enhance our testing strategies, drive innovation, and contribute to the continuous improvement of our firmware development process.
Join our dynamic team at Sonsoft Inc. as a Ranorex Automation Engineer. In this role, you'll leverage your skills in automation testing to enhance our software quality and efficiency. You will be responsible for designing, developing, and executing automated test scripts using Ranorex. Collaborate with cross-functional teams to ensure seamless integration and functionality across various platforms.
Join Sonsoft Inc. as a Ranorex Automation Engineer in vibrant Boston, Massachusetts! We are looking for a detail-oriented and skilled engineer to enhance our automation capabilities. You will collaborate with cross-functional teams to develop and maintain automated testing frameworks using Ranorex. This role is perfect for individuals passionate about software quality assurance and automation.
About the Role Great Gray Group is hiring a Senior QA Automation Engineer in Boston, MA. This role focuses on strengthening the quality of software products by creating and maintaining automated test frameworks. The work directly supports the reliability and stability of applications through thorough testing. What You Will Do Design, build, and maintain automated test frameworks Develop and execute rigorous testing protocols to validate application quality Advise and support the development team on quality assurance best practices Help foster a culture focused on software excellence
Full-time|$73K/yr - $76K/yr|Hybrid|Boston, Massachusetts, United States
Role OverviewKey Responsibilities: As a Statistician, you will design and implement statistical analysis plans, effectively communicating methodologies and outcomes to clients within the healthcare industry.Salary: $73,000 to $76,000, commensurate with qualifications and prior experience.Benefits: Enjoy discretionary profit share bonuses paid biannually, hybrid working arrangements, a generous vacation policy, private medical and dental coverage, a 401K plan with up to a 5% employer match, life insurance, and full funding for external training along with study leave. For more details, visit our benefits page.Employment Type: Full-time, permanent.Start Date: We are looking to fill positions with a start date in early 2026; please indicate your availability in your application.Application Deadline: There are no strict deadlines, but we encourage early applications as positions may close once suitable candidates are identified.Location: This opportunity is based in our Boston office.About the RoleJoin our Statistics team at Costello Medical, where we deliver exceptional statistical and analytical expertise. You will devise statistical analysis plans and conduct data analysis utilizing R, Excel, Stan, SQL, and BUGS software. Your work will involve analyzing various datasets, including patient-level clinical trial data, real-world observational studies, and published aggregate data. Techniques employed range from basic statistical analysis to complex Bayesian network meta-analysis.Collaborating with a diverse team of professionals, you will ensure that all statistical projects meet high standards and are delivered on time, aligning with client expectations. Comprehensive training will be provided in both technical skills and client communication to support your professional growth.
At Klaviyo, we celebrate the diverse backgrounds, experiences, and perspectives our team members—whom we affectionately refer to as Klaviyos—bring to our innovative workplace. We believe that everyone deserves an equitable opportunity for success and value the unique insights each individual contributes beyond conventional job qualifications. If you feel you are close to the mark but may not meet every requirement, we encourage you to apply. Curious about life at Klaviyo? Visit klaviyo.com/careers to explore how we empower creators to take charge of their own destinies.At Klaviyo, we thrive on overcoming complex engineering challenges and seek engineers who have specialized skills yet are passionate about building, owning, and scaling features from inception to completion, while overcoming any hurdles or technical challenges that arise. We inspire one another to step outside our comfort zones, embrace new technologies, and strive to make each day an improvement over the last.Team Overview:Klaviyo operates a cutting-edge real-time data analytics platform primarily developed in Python, designed to handle extensive scale and hosted on Amazon Web Services (AWS). The Data Automation team is responsible for creating tools and establishing best practices that empower our Data Platform, fueling core Klaviyo functionalities and generating insightful, data-driven results.As a foundational member of the Data Automation team, you will define both the technical and organizational vision for the team. Your leadership will guide the design and development of systems critical to our analytics infrastructure.Team Tech Stack:AWSTerraformPythonKubernetesClickhouseDynamoDBMySQLKafkaSparkFlinkAirflowHow You’ll Make an Impact:Lead and nurture a team of 7+ engineers to realize your data automation vision and roadmap.Coach engineers, oversee and review technical documentation, and articulate a phased approach to project execution.
Full-time|$73K/yr - $76K/yr|Hybrid|Boston, Massachusetts, United States
Role SummaryAs a Health Economist at Costello Medical, you will play a pivotal role in shaping healthcare decisions by developing economic models that assist in the effective allocation of resources within the healthcare sector. You will be tasked with communicating critical insights to a diverse range of stakeholders.About the RoleIn this challenging yet rewarding position, you will create quantitative assessments that evaluate the impact of healthcare treatments, practices, and policies. This will involve conducting cost-effectiveness analyses and separate cost and benefit evaluations using advanced tools such as Microsoft Excel, R, or C++. Your work will frequently include fitting statistical distributions and parametric survival curves to clinical data, thus a strong knowledge of statistics is essential. You can expect to manage multiple projects simultaneously, typically 3 to 4, upon joining our team.The economic models you develop will have significant real-world implications, aimed at enhancing the efficiency of healthcare systems through robust methodological frameworks. Your responsibilities will include:Conducting thorough research and critical appraisal of medical and economic literatureCollaborating and building relationships with external medical professionalsWorking as part of a team across various healthcare disciplinesApplying theoretical health economic frameworks to project needs
Full-time|$58K/yr - $60K/yr|Hybrid|Boston, Massachusetts, United States
Role OverviewKey Responsibilities: In this dynamic role, you will undertake a diverse range of administrative, coordination, and scientific tasks associated with client projects, while also contributing to various company and team initiatives.Compensation: The position offers a starting salary of $58,000 annually, which increases to $60,000 for candidates holding a master’s degree. Please note that this salary is fixed and non-negotiable.Employee Benefits: Enjoy a hybrid working model that allows up to 50% remote work, generous holiday leave, flexible working hours, comprehensive private medical and dental insurance, a 401K plan, life insurance, complete funding for external training, extensive travel insurance, and many more benefits.Employment Type: This is a full-time, permanent position.Start Date: We are currently recruiting for positions starting in early 2026.Office Location: This role is based in our Boston office.About the PositionAs a Project Coordinator, you will be an integral part of our scientific teams, engaging in a wide array of administrative, project management, and scientific activities. These teams cover areas such as Medical Communications, Market Access, Evidence Development, and Rare Diseases. During the recruitment process, we will explore your interests in these areas, assigning you to a specific team upon joining. Many Project Coordinators also have the opportunity to work across different teams, enhancing their exposure to various project types and responsibilities.Your role will primarily focus on ensuring the successful delivery of scientific work to our healthcare clients, overseeing the smooth execution of projects and contributing to the overall effectiveness of our operations.
Join our innovative team at Sons of Soft Inc. as a Ranorex Automation Engineer. In this role, you will leverage your expertise in automation testing to enhance software quality and streamline testing processes. We are looking for a passionate engineer who thrives in a collaborative environment and is eager to tackle challenging projects.
Join our innovative team at hike-medical as a Senior Product Designer, where you will play a crucial role in shaping the future of healthcare technology. We are looking for a creative and experienced designer who is passionate about user-centered design and has a strong portfolio showcasing impactful design solutions.In this role, you will collaborate with cross-functional teams to conceptualize and develop user-friendly products that enhance patient experiences. Your expertise in design thinking and your ability to translate complex problems into elegant solutions will be vital to our mission.
Join our innovative team at System Canada Technologies as a Medical Devices Automation Engineer. In this role, you will spearhead automation processes to enhance the efficiency and reliability of our medical device manufacturing. You will collaborate with cross-functional teams to develop and implement automation strategies, ensuring compliance with industry…
About Beacon Biosignals Beacon Biosignals is advancing precision medicine for brain health. The company’s at-home EEG platform supports clinical development of new therapeutics for neurological, psychiatric, and sleep disorders. Beacon’s FDA 510(k)-cleared Waveband EEG headband and proprietary AI algorithms enable quantitative biomarker discovery and application. With a Clinico-EEG database spanning nearly 100,000 patients, Beacon’s cloud-native analytics platform powers large-scale retrospective and predictive studies using real-world data. The team is working to redefine treatment for conditions affecting brain physiology. Role Overview: Director of Device Engineering The Director of Device Engineering leads a multidisciplinary team focused on hardware and systems engineering. Reporting to the VP of Device Engineering, this leader shapes and executes the device engineering strategy while overseeing daily operations and team development. Key Responsibilities Guide the full lifecycle of home sleep testing products, from concept and architecture through verification, regulatory submission, manufacturing transfer, commercialization, and ongoing support. Deliver safe, reliable, and high-quality medical devices that meet clinical needs, regulatory requirements, and business goals. Direct product support efforts, including vendor and contract manufacturer management, resolving production issues, improving yields, and implementing design changes to enhance reliability, performance, and scalability. Collaborate with Quality Assurance, Regulatory Affairs, Clinical Operations, and Logistics teams to uphold rigorous design controls, risk management, and audit readiness in line with medical device regulations. Maintain high standards for safety, compliance, system integrity, and product quality as the company grows. Location This position is based in the Boston area to support close collaboration with the local team.
Full-time|On-site|Boston, Massachusetts, United States
TransPerfect delivers language services and technology solutions to enterprise clients worldwide. With operations in more than 100 cities and support for over 170 languages, the company helps organizations manage multilingual content efficiently through its GlobalLink® platform. TransPerfect holds ISO 9001 and ISO 17100 certifications. Headquarters are in New York, with additional offices in London and Hong Kong. More information is available at www.transperfect.com. Role overview The Account Executive for the medical device sector develops new business and supports existing clients in the Boston area. This role expands TransPerfect’s presence and strengthens partnerships within the medical device industry. What you will do Drive business development in the region to create new revenue opportunities. Identify and reach out to potential clients through online research, trade shows, referrals, and professional networks. Engage new clients using cold calling, networking, and participation in industry events. Design and implement sales strategies to meet monthly, quarterly, and annual targets. Present TransPerfect’s solutions in both virtual and in-person meetings, adapting to client needs. Refine business development tactics specific to the medical device market. Negotiate pricing and project timelines with new and existing clients. Explain the translation process, pricing, turnaround times, and how TransPerfect compares with competitors. Develop account strategies at regional and national levels to achieve revenue and margin goals. Build a strong understanding of TransPerfect’s services and their value in the market. Deepen relationships with key customers and broaden engagement across accounts. Location Boston, Massachusetts, United States
The Account Executive, Medical Devices and Life Sciences role at InterSystems focuses on driving growth in these sectors from the Boston office. The position centers on building strong relationships with both new prospects and existing customers, supporting the expansion of the HealthShare platform. HealthShare connects patient data and enables interoperability and analytics for healthcare organizations. Key responsibilities Promote InterSystems products and services to organizations in the medical devices and life sciences fields, prioritizing new business development. Create and implement sales strategies to increase revenue within assigned accounts. Act as the main contact for customer organizations, strengthening connections at various levels. Work closely with internal teams to meet sales goals and deliver value to clients. Collect and communicate customer feedback on products to support ongoing improvements. Grow new business revenue while maintaining and expanding relationships with current customers. Location This position is based in Boston, MA.
About Hike MedicalHike Medical is revolutionizing musculoskeletal care, beginning with foot health. Our innovative AI-driven vision platform transforms a quick 30-second web-based foot scan into custom-engineered, 3D-printed insoles that help prevent pain before it occurs. We are already safeguarding the well-being of on-their-feet workforces at Fortune 50 companies, significant health systems, and manufacturers across middle America. Recently funded by top-tier venture capitalists, we maintain a fast-paced, no-nonsense execution culture from our Boston Seaport headquarters as we aim for $100M ARR and to support 10 million Americans in their daily lives.First and only PDAC-approved 3D printed custom insole globally Three proprietary AI models enhancing the user experienceTwo product lines: one for employers & health plans, and another for clinics to provide affordable foot care, creating a beneficial cycle of clinician-validated data.Expanded access to care for over 100,000 Americans to dateRevenue growth of 10x from 2023 to 2024, with projections to continue this trend in 2025. Consistently profitable month-over-month.The RoleAs a Senior Software Engineer, you will develop and deploy the essential systems behind Hike’s AI healthcare platform. Serving as the backbone of Hike's rapidly growing, mission-driven initiative, you will design scalable services, implement production-ready AI, and create user experiences that enhance patient outcomes. From your first day, you will enjoy significant autonomy and a direct impact on transforming the US healthcare landscape.Why This Opportunity is Career-Defining:Your code will empower individuals to move without pain.You will have complete autonomy to create, deploy, and witness the outcomes—transitioning from concept to production in mere hours or days.You’ll collaborate with a high-performing team of elite engineers and AI researchers, where every addition substantially influences our mission.You'll thrive in a culture that rejects bureaucracy, discourages unnecessary complexity, and values trust as our core principle.What You'll Work On:Architect, build, and refine high-performance, scalable systems that drive AI-based solutions.Design resilient, serverless architectures within a TypeScript and AWS environment.Create developer-friendly APIs and SDKs to enhance integration and usability.
About SimpliSafe At SimpliSafe, we are an innovative home security company dedicated to safeguarding the life you've built. Our mission is to ensure that Every Home is Secure. We foster a culture that values your professional growth as much as our commitment to our customers. With an ego-free environment that encourages collaboration and innovation, we welcome individuals who are passionate about making a significant impact in the home security industry. We don’t just want you to work here; we want you to flourish and succeed. We embrace a hybrid work model, allowing our teams to balance their time between the office and home. Our hybrid approach typically requires in-person collaboration on two core days, often Tuesday, Wednesday, or Thursday, while providing the flexibility to work remotely the rest of the week. This model enables us to leverage the best of both worlds for our productivity. Why Join Us? As we continue to grow, we seek talented, intelligent, and humble individuals who align with our values and are eager to join us in revolutionizing the home security landscape while pursuing our mission of keeping Every Home Secure. Your Role You will be part of SimpliSafe’s Device Cloud Services team, striving to enhance cloud-based systems that allow customers to manage their home security from anywhere globally. We are in search of a driven and experienced Senior Software Engineer to architect, develop, maintain, and take ownership of software solutions. As a backend team, we tackle large-scale distributed challenges, ensuring our customers enjoy real-time access and control over their security systems. Our core principles revolve around life safety, reliability, simplicity, and performance. Key Responsibilities: Design and develop robust solutions, mentoring junior engineers to grasp product requirements and create scalable, reliable systems. Implement and maintain tests to ensure high-level functionality and safe refactoring of solutions. Engage in long-term support and maintenance tasks, including performance optimization, bug fixes, feature enhancements, design improvements, and automation. Document the systems you develop to facilitate future maintenance and upgrades by subsequent developers. Act as an on-call first responder for software under your team's purview.
Full-time|$141K/yr - $225.6K/yr|Hybrid|Boston, Massachusetts, United States
Join Axon and be a Force for Good.At Axon, our mission is to Protect Life. We are pioneers tackling some of society's most pressing safety and justice challenges through our innovative ecosystem of devices and cloud software. We thrive on collaboration, fostering open communication and valuing diverse perspectives from our customers, communities, and each other.Life at Axon is dynamic, rewarding, and impactful. Here, you’ll take ownership and effect real change, growing constantly as you contribute to a mission that truly matters at a company that values you. Your ImpactAs a member of our high-performing software engineering team, you will develop embedded software for Axon’s devices, ensuring critical evidence is captured during vital moments for our customers. This role offers the chance to collaborate with talented software and firmware engineers and to contribute to the development of next-generation public safety products, including body-worn cameras, in-car cameras, and wireless microphones.Your role requires you to engage deeply in architectural decisions that will influence our products. You are committed to crafting device software characterized by high stability and rapid, consistent performance. With a passion for working with cutting-edge open-source technologies, you will leverage your systems design expertise to make sound technical decisions for robust systems.In addition to driving decisions among competing engineering trade-offs, your empathy for customers will enable you to propose innovative solutions to their challenges. You will work closely with product managers and designers to ensure we are developing the right solutions for our customers. Furthermore, you enjoy mentoring fellow engineers, acting as a hands-on teacher to elevate the team around you.As an Embedded Application Software Engineer, your responsibilities will include designing, developing, testing, and maintaining embedded applications and networking configurations, along with the necessary systems and libraries, while interfacing with cloud and firmware services for the devices. Join our mission-driven team eager to positively impact the lives of first responders and those they serve.
Full-time|Hybrid|Boston, Massachusetts, United States
Job Title: Senior Sustaining EngineerLocation: Boston, MAEmployment Type: Full-time (Hybrid) About Activ SurgicalActiv Surgical is a pioneering medical device startup dedicated to revolutionizing surgical advanced visualization through innovative imaging, computer vision, and artificial intelligence technologies. Our platform seamlessly integrates state-of-the-art solutions to elevate laparoscopic and minimally invasive surgical procedures. Position OverviewAs a Senior Sustaining Engineer, you will take charge of the manufacturing processes, sustaining efforts, and continuous improvements for the Activ Surgical platform. Acting as the primary technical liaison with our contract manufacturer, you will facilitate cross-departmental collaboration across Quality, Regulatory, Operations, and R&D teams. This role blends hands-on engineering expertise with structured problem-solving and detailed documentation in a dynamic startup environment.Your duties will encompass sustaining engineering, investigating hardware issues, implementing design-for-manufacture strategies, and managing the product development cycle for our existing platform. You will collaborate closely with Quality and Regulatory teams on handling complaints, non-conformance reports (NCRs), corrective and preventive actions (CAPAs), and field investigations, ensuring the device adheres to reliability, manufacturability, and compliance standards. Key ResponsibilitiesManufacturing Leadership & Technical InterfaceAct as the primary technical contact for the contract manufacturer, assisting with daily production, troubleshooting, and ensuring build readiness.Lead the resolution of manufacturing challenges, including assembly difficulties, test failures, yield enhancements, and line-down incidents.Review, approve, and contribute to updates in manufacturing documentation, including work instructions, testing procedures, and assembly processes.Drive the implementation of engineering change orders (ECOs) while ensuring compliant and controlled distribution at the contract manufacturer.Support manufacturing preparedness for engineering builds, pilot runs, and ongoing production.Sustaining Engineering & Quality InvestigationsLead root-cause analysis and corrective action initiatives for hardware-related issues, including complaints, NCRs, CAPAs, and field returns.Collaborate with Quality and Regulatory teams to ensure investigations and enhancements comply with ISO 13485 and FDA Quality System Regulations (QSR).Oversee sustaining engineering tasks to bolster reliability, robustness, and performance of the current hardware platform.Maintain hardware documentation and facilitate updates to risk management, verification, and traceability as necessary.Design for Manufacture & Process EnhancementsChampion design for manufacture (DFM), design for assembly (DFA), and process improvement initiatives aimed at increasing manufacturability, reducing costs, and optimizing assembly/testing workflows.
Full-time|$70K/yr - $73K/yr|Hybrid|Boston, Massachusetts, United States
Role Summary Responsibilities: Engage in projects that demand thorough analysis and presentation of clinical data, crucial for the successful adoption of innovative therapies. Salary: $70,000 to $73,000 per annum based on prior experience (this is a standardized, non-negotiable salary). Benefits: Enjoy hybrid working arrangements allowing up to 50% remote work, generous vacation allowance, flexible hours, private medical and dental coverage, 401K plan, life insurance, full funding for external training, comprehensive travel insurance, and more. Role Type: Full-time, permanent. Start Date: We are currently recruiting for positions starting in 2026. Location: This opportunity is based in our Boston office. About the RoleThe Analyst and Medical Writer roles are perfect for recent science graduates or those with scientific research experience, eager to apply their knowledge to impactful projects. These professionals will analyze clinical trial data and creatively present findings through various formats such as posters, slide sets, value dossiers, reports, and peer-reviewed publications. These deliverables play a vital role in our clients' communications with external stakeholders, facilitating the successful adoption of novel therapies. Work is organized on a project basis, involving three to four concurrent projects across a range of prominent disease areas and products, offering a diverse work experience and opportunities to develop a broad skill set.Collaboration is key, as you will work closely with seasoned colleagues who will provide training in both technical aspects and project management, as well as effective client communication. Your role will involve direct engagement with clients, with opportunities for teleconferences and in-person meetings, which may include travel within the US and internationally.Located in our Boston office, established in 2020, this role offers the chance to shape and influence our US operations, building on the success of our established presence in the UK and Asia. You will closely collaborate with our Scientific Director based in Boston.
Internship|$24/hr - $30/hr|On-site|Boston, Massachusetts, United States
Role OverviewKey Responsibilities: Engage in hands-on projects across Medical Communications, Evidence Development, and Value and Access domains, focusing on the assimilation, interpretation, and innovative presentation of scientific data related to pharmaceuticals and medical devices.Compensation: Competitive hourly wage ranging from $24 to $30, contingent on experience.Benefits: Enjoy a generous vacation leave policy, flexible working hours, the option to work from home one day per week, comprehensive medical, dental, and vision insurance, plus opportunities for social activities funded by the company.Role Type: Full-time, 3-month internship.Start Date: We are currently seeking candidates for Summer 2026; please indicate your availability on your application.Location: This position is based in our Boston office.About the InternshipThis Analyst/Medical Writer Internship is tailored for current students and recent graduates from scientific backgrounds looking to gain valuable insights into the operations of a premier healthcare consultancy. Interns will contribute to two to three distinct projects, involving tasks such as:Creating medical education presentationsConducting systematic literature reviewsDrafting clinical trial manuscriptsCompiling clinical and cost-effectiveness evidence to support HTA submissions to NICEThese impactful projects play a vital role in enhancing global healthcare outcomes. Interns will receive personalized training on the technical aspects of their roles and gain insights into project management and effective client communication.
Join SimpliSafe, a leader in home security technology, as a Senior Firmware Automation Engineer. In this pivotal role, you will be responsible for developing, implementing, and optimizing automated testing frameworks to ensure the highest quality of our firmware products. You will collaborate with cross-functional teams to enhance our testing strategies, drive innovation, and contribute to the continuous improvement of our firmware development process.
Join our dynamic team at Sonsoft Inc. as a Ranorex Automation Engineer. In this role, you'll leverage your skills in automation testing to enhance our software quality and efficiency. You will be responsible for designing, developing, and executing automated test scripts using Ranorex. Collaborate with cross-functional teams to ensure seamless integration and functionality across various platforms.
Join Sonsoft Inc. as a Ranorex Automation Engineer in vibrant Boston, Massachusetts! We are looking for a detail-oriented and skilled engineer to enhance our automation capabilities. You will collaborate with cross-functional teams to develop and maintain automated testing frameworks using Ranorex. This role is perfect for individuals passionate about software quality assurance and automation.
About the Role Great Gray Group is hiring a Senior QA Automation Engineer in Boston, MA. This role focuses on strengthening the quality of software products by creating and maintaining automated test frameworks. The work directly supports the reliability and stability of applications through thorough testing. What You Will Do Design, build, and maintain automated test frameworks Develop and execute rigorous testing protocols to validate application quality Advise and support the development team on quality assurance best practices Help foster a culture focused on software excellence
Full-time|$73K/yr - $76K/yr|Hybrid|Boston, Massachusetts, United States
Role OverviewKey Responsibilities: As a Statistician, you will design and implement statistical analysis plans, effectively communicating methodologies and outcomes to clients within the healthcare industry.Salary: $73,000 to $76,000, commensurate with qualifications and prior experience.Benefits: Enjoy discretionary profit share bonuses paid biannually, hybrid working arrangements, a generous vacation policy, private medical and dental coverage, a 401K plan with up to a 5% employer match, life insurance, and full funding for external training along with study leave. For more details, visit our benefits page.Employment Type: Full-time, permanent.Start Date: We are looking to fill positions with a start date in early 2026; please indicate your availability in your application.Application Deadline: There are no strict deadlines, but we encourage early applications as positions may close once suitable candidates are identified.Location: This opportunity is based in our Boston office.About the RoleJoin our Statistics team at Costello Medical, where we deliver exceptional statistical and analytical expertise. You will devise statistical analysis plans and conduct data analysis utilizing R, Excel, Stan, SQL, and BUGS software. Your work will involve analyzing various datasets, including patient-level clinical trial data, real-world observational studies, and published aggregate data. Techniques employed range from basic statistical analysis to complex Bayesian network meta-analysis.Collaborating with a diverse team of professionals, you will ensure that all statistical projects meet high standards and are delivered on time, aligning with client expectations. Comprehensive training will be provided in both technical skills and client communication to support your professional growth.
At Klaviyo, we celebrate the diverse backgrounds, experiences, and perspectives our team members—whom we affectionately refer to as Klaviyos—bring to our innovative workplace. We believe that everyone deserves an equitable opportunity for success and value the unique insights each individual contributes beyond conventional job qualifications. If you feel you are close to the mark but may not meet every requirement, we encourage you to apply. Curious about life at Klaviyo? Visit klaviyo.com/careers to explore how we empower creators to take charge of their own destinies.At Klaviyo, we thrive on overcoming complex engineering challenges and seek engineers who have specialized skills yet are passionate about building, owning, and scaling features from inception to completion, while overcoming any hurdles or technical challenges that arise. We inspire one another to step outside our comfort zones, embrace new technologies, and strive to make each day an improvement over the last.Team Overview:Klaviyo operates a cutting-edge real-time data analytics platform primarily developed in Python, designed to handle extensive scale and hosted on Amazon Web Services (AWS). The Data Automation team is responsible for creating tools and establishing best practices that empower our Data Platform, fueling core Klaviyo functionalities and generating insightful, data-driven results.As a foundational member of the Data Automation team, you will define both the technical and organizational vision for the team. Your leadership will guide the design and development of systems critical to our analytics infrastructure.Team Tech Stack:AWSTerraformPythonKubernetesClickhouseDynamoDBMySQLKafkaSparkFlinkAirflowHow You’ll Make an Impact:Lead and nurture a team of 7+ engineers to realize your data automation vision and roadmap.Coach engineers, oversee and review technical documentation, and articulate a phased approach to project execution.
Full-time|$73K/yr - $76K/yr|Hybrid|Boston, Massachusetts, United States
Role SummaryAs a Health Economist at Costello Medical, you will play a pivotal role in shaping healthcare decisions by developing economic models that assist in the effective allocation of resources within the healthcare sector. You will be tasked with communicating critical insights to a diverse range of stakeholders.About the RoleIn this challenging yet rewarding position, you will create quantitative assessments that evaluate the impact of healthcare treatments, practices, and policies. This will involve conducting cost-effectiveness analyses and separate cost and benefit evaluations using advanced tools such as Microsoft Excel, R, or C++. Your work will frequently include fitting statistical distributions and parametric survival curves to clinical data, thus a strong knowledge of statistics is essential. You can expect to manage multiple projects simultaneously, typically 3 to 4, upon joining our team.The economic models you develop will have significant real-world implications, aimed at enhancing the efficiency of healthcare systems through robust methodological frameworks. Your responsibilities will include:Conducting thorough research and critical appraisal of medical and economic literatureCollaborating and building relationships with external medical professionalsWorking as part of a team across various healthcare disciplinesApplying theoretical health economic frameworks to project needs
Full-time|$58K/yr - $60K/yr|Hybrid|Boston, Massachusetts, United States
Role OverviewKey Responsibilities: In this dynamic role, you will undertake a diverse range of administrative, coordination, and scientific tasks associated with client projects, while also contributing to various company and team initiatives.Compensation: The position offers a starting salary of $58,000 annually, which increases to $60,000 for candidates holding a master’s degree. Please note that this salary is fixed and non-negotiable.Employee Benefits: Enjoy a hybrid working model that allows up to 50% remote work, generous holiday leave, flexible working hours, comprehensive private medical and dental insurance, a 401K plan, life insurance, complete funding for external training, extensive travel insurance, and many more benefits.Employment Type: This is a full-time, permanent position.Start Date: We are currently recruiting for positions starting in early 2026.Office Location: This role is based in our Boston office.About the PositionAs a Project Coordinator, you will be an integral part of our scientific teams, engaging in a wide array of administrative, project management, and scientific activities. These teams cover areas such as Medical Communications, Market Access, Evidence Development, and Rare Diseases. During the recruitment process, we will explore your interests in these areas, assigning you to a specific team upon joining. Many Project Coordinators also have the opportunity to work across different teams, enhancing their exposure to various project types and responsibilities.Your role will primarily focus on ensuring the successful delivery of scientific work to our healthcare clients, overseeing the smooth execution of projects and contributing to the overall effectiveness of our operations.
Join our innovative team at Sons of Soft Inc. as a Ranorex Automation Engineer. In this role, you will leverage your expertise in automation testing to enhance software quality and streamline testing processes. We are looking for a passionate engineer who thrives in a collaborative environment and is eager to tackle challenging projects.
Join our innovative team at hike-medical as a Senior Product Designer, where you will play a crucial role in shaping the future of healthcare technology. We are looking for a creative and experienced designer who is passionate about user-centered design and has a strong portfolio showcasing impactful design solutions.In this role, you will collaborate with cross-functional teams to conceptualize and develop user-friendly products that enhance patient experiences. Your expertise in design thinking and your ability to translate complex problems into elegant solutions will be vital to our mission.
Mar 13, 2026
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