Field Application Scientist - Image and Detection Systems (Northeast United States) Thermo Fisher ScientificField Application Scientist - Image and Detection Systems (Northeast United States)Waltham, MassachusettsAs a Field Application Scientist (FAS) supporting our Imaging & Detection portfolio, you will serve as the scientific and technical expert for customers throughout the evaluation, implementation, and ongoing use of Thermo Fisher Scientific's imaging and detection platforms, including EVOS microscopes, Celleste Image Analysis Software, Varioskan multimode plate readers, iBright imaging systems, and emerging technologies. In this customer-facing role, you will partner with academic researchers, biotechnology companies, pharmaceutical organizations, and core laboratory facilities to optimize experimental workflows, troubleshoot scientific challenges, and enable successful adoption of our technologies.
Project Manager, Internal Evaluations (Hybrid - Acton, MA) Insulet CorpProject Manager, Internal Evaluations (Hybrid - Acton, MA)Acton, MA$90,500–$135,800 / yearInsulet's flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Responsibilities: Partner with Program Managers to ensure programs are managed efficiently and effectively by participating and driving all phase of development starting with concept through design transfer.
Electrical Engineer LancesoftElectrical EngineerBurlington, MA$40Analyzes failures, develops, and implements investigative protocols to identify root causes, performs circuit analysis, performs device and component level failure analysis. May serve as lead and assign work to less experienced personnel and serves as a mentor when assisting less experienced lab staff in solving more complex problems.
Senior Technical Product Manager Beacon BiosignalsSenior Technical Product ManagerBoston, Massachusetts$147,000–$167,000 / yearAs such, we're always seeking new contributors whose work demonstrates an avid curiosity, a bias towards simplicity, an eye for composability, a self-service mindset, and - most of all - a deep empathy towards colleagues, stakeholders, users, and patients. Partner closely with Systems, Hardware, Firmware, Software, Algorithms, Clinical, Quality, Regulatory, Business Development, Operations, and Manufacturing teams to drive successful product development and commercialization.
Senior Technical Product Manager Beacon Biosignals, IncSenior Technical Product ManagerBoston, MA$147,000–$167,000 / yearAs such, we're always seeking new contributors whose work demonstrates an avid curiosity, a bias towards simplicity, an eye for composability, a self-service mindset, and - most of all - a deep empathy towards colleagues, stakeholders, users, and patients. Partner closely with Systems, Hardware, Firmware, Software, Algorithms, Clinical, Quality, Regulatory, Business Development, Operations, and Manufacturing teams to drive successful product development and commercialization.
Usability And Regulatory Affairs Specialist SentecUsability And Regulatory Affairs SpecialistLincoln, RI$90,000–$110,000 / yearDevelop and maintain usability engineering documentation, including use specifications, task analyses, use-related risk analyses, and the usability engineering file, in accordance with IEC 62366 and FDA guidance. You will work closely with engineering, clinical, and quality teams to identify and mitigate use-related risks—ultimately helping bring high-impact medical technologies to market.
Sr. Software Product Owner MedtronicSr. Software Product OwnerBoston, MassachusettsMust possess at least two (2) years’ experience with each of the following: Hybrid hardware and software (HW/SW) product using scaled agile framework; C++, Python, and Simulink; SDLC - AUTOSAR and tools to include JIRA, Bitbucket, Stash, Confluence, JAMA, Git, and CMake; ISO 13485, ISO 14971, ISO 26262, ASPICE, or SOTIF; FMEA; Software architecture, design specifications, anomaly tracking, and test reports, supporting compliance and audit readiness; Software release planning and coordination; Embedded systems development, including firmware and hardware integration; and Embedded software architectures, real-time operating systems (RTOS), and debugging tools. Navigate medical devices and other industry regulations such as ISO 13485, ISO 14971, ISO 26262, Good Manufacturing Practices (GMP) guidelines, Automotive Software Process Improvement and Capability Determination (ASPICE), Safety Of The Intended Functionality (SOTIF), FDA 21 CFR Part 802 regulations, and IEC 62304.
Usability Specialist SentecUsability SpecialistLincoln, RI$90,000–$110,000 / yearDevelop and maintain usability engineering documentation, including use specifications, task analyses, use-related risk analyses, and the usability engineering file, in accordance with IEC 62366 and FDA guidance. You will work closely with engineering, clinical, and quality teams to identify and mitigate use-related risks—ultimately helping bring high-impact medical technologies to market.
Sr. Software Product Owner Medtronic PlcSr. Software Product OwnerBoston, MA$149,000–$177,600 / yearMust possess at least two (2) years' experience with each of the following: Hybrid hardware and software (HW/SW) product using scaled agile framework; C++, Python, and Simulink; SDLC - AUTOSAR and tools to include JIRA, Bitbucket, Stash, Confluence, JAMA, Git, and CMake; ISO 13485, ISO 14971, ISO 26262, ASPICE, or SOTIF; FMEA; Software architecture, design specifications, anomaly tracking, and test reports, supporting compliance and audit readiness; Software release planning and coordination; Embedded systems development, including firmware and hardware integration; and Embedded software architectures, real-time operating systems (RTOS), and debugging tools. Navigate medical devices and other industry regulations such as ISO 13485, ISO 14971, ISO 26262, Good Manufacturing Practices (GMP) guidelines, Automotive Software Process Improvement and Capability Determination (ASPICE), Safety Of The Intended Functionality (SOTIF), FDA 21 CFR Part 802 regulations, and IEC 62304.
NewSenior Technical Product Manager Beacon Biosignals IncSenior Technical Product ManagerBoston, MA$147,000–$167,000 / yearAs such, we''re always seeking new contributors whose work demonstrates an avid curiosity, a bias towards simplicity, an eye for composability, a self-service mindset, and - most of all - a deep empathy towards colleagues, stakeholders, users, and patients. Partner closely with Systems, Hardware, Firmware, Software, Algorithms, Clinical, Quality, Regulatory, Business Development, Operations, and Manufacturing teams to drive successful product development and commercialization.
New2027 Spring Co Op Device Strategy And Innovation Cambridge MA Sanofi2027 Spring Co Op Device Strategy And Innovation Cambridge MACambridge, MA$29–$57 / hourStudents currently on CPT, OPT, or STEM OPT usually require future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship. If you are excited about contributing to the development of breakthrough drug delivery devices to address the delivery needs for our current and future pipeline portfolio, we encourage you to apply and be part of our collaborative and forward-thinking research team at Sanofi.
Associate Director, Device Lead GSK plcAssociate Director, Device LeadWaltham, MA$142,725–$237,875 / yearThese responsibilities include some of the following: Be the SPOC technical SME interface between Device/Component suppliers and GSK MSAT site teams - providing device-related technical management to MSAT where required for business improvement projects and risk management activities, represent MSAT at supplier technical and project meetings. Drive innovation through the introduction of new and novel device technologies and/or ways of working and champion business cases for sustainable manufacturing technology implementation or other strategic projects including those related to quality by design, design for manufacturing, product and process understanding, design control, and digital data management, and analytical competency.
New2027 Spring Co op Device Strategy and Innovation Cambridge MA Sanofi2027 Spring Co op Device Strategy and Innovation Cambridge MACambridge, MA$29–$57 / hourStudents currently on CPT, OPT, or STEM OPT usually require future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship. If you are excited about contributing to the development of breakthrough drug delivery devices to address the delivery needs for our current and future pipeline portfolio, we encourage you to apply and be part of our collaborative and forward-thinking research team at Sanofi.
NewProgram Coordinator II, Part Time Mass General BrighamProgram Coordinator II, Part TimeBoston, Massachusetts$22.22–$31.71 / hourThe Central Venous Catheter (CVC) Program Coordinator provides administrative and operational support to the MGB CVC Safe Insertion Training and Competency Program across Massachusetts General Hospital (MGH) and Brigham and Women’s Hospital (BWH), operating under the AMC Office of the Chief Medical Officer. Assist the Co-Program Medical Directors with periodic updates to HealthStream (HS) training modules, including US-guided IJ CVC placement, CLABSI prevention, CVC observation, subclavian catheter placement, and US-guided peripheral IV access (SonoSite and SiteRite systems).
Scientist II, LNP CRISPR Therapeutics AGScientist II, LNPSouth Boston, MA$130,000–$140,000 / yearThe Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY (exagamglogene autotemcel [exa-cel]), the world's first CRISPR-based therapy, approved for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia. The ideal candidate will have experience in lipid nanoparticle (LNP) design, formulation and characterization, with proven experience in designing novel solutions for encapsulation of different nucleic acid payloads (such as mRNA, siRNA, etc.).
Associate Director, Device Development Rhythm PharmaceuticalsAssociate Director, Device DevelopmentBoston, MA$160,000–$240,000 / yearYou will serve as the device subject matter expert (SME), accountable for design control execution, design history file (DHF) ownership, and integration of device strategy across CMC, regulatory, clinical, and manufacturing functions. Opportunity Overview As an Associate Director, Device Development , you will lead the development and lifecycle management of drug–device combination products, with a focus on injectable delivery systems such as prefilled syringes and auto-injectors.
Head Of Regulatory, AM & D PhilipsHead Of Regulatory, AM & DCambridge, MA$171,000–$273,000 / yearPartner cross-functionally to integrate regulatory requirements into product development and business processes, leading regulatory planning, risk assessments, and compliance strategies while driving continuous improvement initiatives that enhance operational efficiency, quality, and regulatory outcomes. Drive regulatory compliance and market access across the product lifecycle, overseeing global product registrations, approvals, CE Marking, clinical evaluations, regulatory submissions, and change management activities to ensure timely commercialization and sustained compliance in international markets.
Rehabilitation Aide Mass General BrighamRehabilitation AideWaltham, MassachusettsThe framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. At Mass General Brigham, our competency framework defines what effective leadership “looks like” by specifying which behaviors are most critical for successful performance at each job level.
Research Fellow, Neuroimaging Mass General BrighamResearch Fellow, NeuroimagingBoston, MassachusettsResponsibilities include participating in all aspects of data acquisition and management; developing, modifying, and executing analytical protocols; preparing publications and scientific presentations; disseminating results in peer-reviewed scientific journals and at major national and international meetings, and mentoring junior staff. Opportunities exist for excellent scientific interactions and collaborations with an extensive program of seminars, symposia, and other meetings focused on a large array of topics in neuroscience, clinical research, and neurotechnology.
NewCo-op - Robotics Mechatronics, Surgical Robotics - Cambridge, MA - January 2027 PhilipsCo-op - Robotics Mechatronics, Surgical Robotics - Cambridge, MA - January 2027Cambridge, MA$29–$32 / hourThe actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity. In this 6-9 month internship, you will work with a multidisciplinary R&D team to design, build, and evaluate a robotic testbed for image-guided surgical robotics applications.