Senior Automation Engineer, Platform Biology Vesalius TherapeuticsSenior Automation Engineer, Platform BiologyCambridge, MA$108,000–$170,700 / yearYou will partner with scientists, automation operators, IT, and data science teams to translate biological workflows into robust automated workcells and ensure experiments generate reliable, traceable, analysis-ready data. Our platform combines large-scale human genetics, genomics, stem cell studies, high-dimensional cellular phenotyping, and artificial intelligence to uncover causal biology and identify optimal intervention points for new therapies.
Senior Automation Engineer, Platform Biology Vesalius Therapeutics IncSenior Automation Engineer, Platform BiologyCambridge, MA$108,000–$170,700 / yearYou will partner with scientists, automation operators, IT, and data science teams to translate biological workflows into robust automated workcells and ensure experiments generate reliable, traceable, analysis-ready data. Our platform combines large-scale human genetics, genomics, stem cell studies, high-dimensional cellular phenotyping, and artificial intelligence to uncover causal biology and identify optimal intervention points for new therapies.
Senior Automation Engineer, Platform Biology Flagship Pioneering IncSenior Automation Engineer, Platform BiologyCambridge, MA$108,000–$170,700 / yearOur platform combines large-scale human genetics, genomics, stem cell studies, high-dimensional cellular phenotyping, and artificial intelligence to uncover causal biology and identify optimal intervention points for new therapies. You will partner with scientists, automation operators, IT, and data science teams to translate biological workflows into robust automated workcells and ensure experiments generate reliable, traceable, analysis-ready data.
Compliance Engineer SharkNinja IncCompliance EngineerNeedham, MA$72,700–$111,400 / yearRelevant discipline context: Biomedical/Bioengineering backgrounds are well-suited to ISO 10993 biocompatibility and clinical evaluation; Systems Engineering to ISO 14971 risk management and design controls; Chemical/Materials Engineering to material selection, substance compliance (REACH, RoHS), and biocompatibility testing; Computer Science/Software Engineering to IEC 62304 software lifecycle and embedded systems compliance. Powered by two trusted, global brands, Shark and Ninja, the company has a proven track record of bringing disruptive innovation to market and developing one consumer product after another has allowed SharkNinja to enter multiple product categories, driving significant growth and market share gains.
Principal Embedded Software Engineer The Charles Stark Draper LaboratoryPrincipal Embedded Software EngineerCambridge, MassachusettsDesign and implement real time operating system, familiarity with processor low-level peripherals such as UART, SPI, DMA controller, memory controller and ability to absorb detail on processor and peripheral operation similar to complex commercial processors and microcontrollers. Draper supports many programs to improve work-life balance including workplace flexibility, employee clubs ranging from photography to yoga, health and finance workshops, off site social events and discounts to local museums and cultural activities.
Fellow in Human-Machine Interface Clinical Research - Bionics Lab Harvard UniversityFellow in Human-Machine Interface Clinical Research - Bionics LabCambridge, MA$50,000–$70,000 / yearThe Harvard John A. Paulson School of Engineering and Applied Sciences (SEAS) Bionics Lab ( https://bioniclab.seas.harvard.edu/ ) is seeking a highly motivated Fellow with a background in Biomedical Engineering, Mechanical Engineering, or Neural Engineering to join our interdisciplinary research team. You will work at the intersection of neuroscience, engineering, and clinical science, gaining hands-on experience with human subject research, robotics, and electrophysiological data analysis, while contributing to impactful translational research.
Mechanical Engineer Integrated Resources, IncMechanical EngineerWestborough, MassachusettsFull timeJob Title: Mechanical Engineer Location: Westborough MA, 01581 Duration: 12 months (Possible extension) Role Summary: A Mechanical Engineer 3 improves product design or designs new product using engineering principles and achieves expertise in mechanical engineering. Engaging in all phases of product redesign for improvement or new product development, including concept, prototype build, test, documentation, supplier interfaces, manufacturing introduction.
Senior Engineer II, Quality Validation Integra LifeSciencesSenior Engineer II, Quality ValidationMassachusettsTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily: Specialized knowledge level, seasoned professional with complete and in-depth conceptual and practical knowledge in one or many areas of Quality Validation. Responsibilities associated with this position are directly associated to review and support validations related to new product introduction (NPI), product transfers, and other validation projects.
Systems Engineer - Ultrasound (Cambridge, MA) PhilipsSystems Engineer - Ultrasound (Cambridge, MA)Cambridge, MA$115,000–$182,000 / yearCollaborate cross-functionally with R&D team members, Marketing, Product Management, and internal/external stakeholders to support new feature requirements for specific clinical applications and market needs, and translate marketing/customer requirements into engineering specifications. Engage with experts in electrical engineering, biomedical engineering, physics, software development, clinical science, and product management to deliver innovative solutions that meet complex clinical and technical requirements.
Senior Design Quality Engineer Katalyst Healthcares & Life SciencesSenior Design Quality EngineerRaynham, MAJob Summary: The Senior Design Quality Engineer will support product lifecycle management activities for medical devices by providing quality engineering leadership for design and process changes, risk management, verification and validation activities, and compliance with medical device regulations. The role requires close collaboration with cross-functional teams including R&D, Manufacturing, Regulatory Affairs, Marketing, and Operations.
Senior Validation Engineer Consultant Katalyst Healthcares & Life SciencesSenior Validation Engineer ConsultantDevens, MASenior CQV Engineer / Senior Validation Engineer with experience supporting commissioning, qualification, and validation activities for process equipment in GMP-regulated environments. Experience working with bioprocess equipment including bioreactors, filtration systems, chromatography systems, and ultrafiltration (UF) preferred.
R&D Engineer Katalyst Healthcares & Life SciencesR&D EngineerRaynham, MAJob Description: The role involves leading integration workstreams, supporting design and quality system integration activities, and collaborating closely with engineering leadership, technical teams, quality, manufacturing, supplier engineering, and regulatory stakeholders. Collaborate closely with engineering managers, technical leads, engineers, and lab/testing support teams in a highly collaborative environment.
Senior CQV Engineer/Senior Validation Engineer Consultant Katalyst Healthcares & Life SciencesSenior CQV Engineer/Senior Validation Engineer ConsultantDevens, MASenior CQV Engineer / Senior Validation Engineer with experience supporting commissioning, qualification, and validation activities for process equipment in GMP-regulated environments. Experience working with bioprocess equipment including bioreactors, filtration systems, chromatography systems, and ultrafiltration (UF) preferred.
Usability & Human Factors Engineer SentecUsability & Human Factors EngineerLincoln, RI$80,000–$100,000Develop 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.
Product Quality Engineer GTTProduct Quality EngineerMarlborough, MAOrganizational Relationships: Works with Divisional personnel and Costa Rica personnel including Product Quality Engineering (PQE), Post Market Quality Engineering (PMQE), and Post Market Analytics. This role will be responsible for reviewing each complaint record individually and identifying the appropriate risk lines and associated severities from the product's Risk Management File (RMF) that relate to what was reported by the complainant and the results of the investigation.
R&D Engineer Karwell TechnologiesR&D EngineerRaynham, MAJob Summary: The role involves leading integration workstreams, supporting design and quality system integration activities, and collaborating closely with engineering leadership, technical teams, quality, manufacturing, supplier engineering, and regulatory stakeholders. Collaborate closely with engineering managers, technical leads, engineers, and lab/testing support teams in a highly collaborative environment.
Senior Design Quality Engineer Karwell TechnologiesSenior Design Quality EngineerRaynham, MAJob Summary: The Senior Design Quality Engineer will support product lifecycle management activities for medical devices by providing quality engineering leadership for design and process changes, risk management, verification and validation activities, and compliance with medical device regulations. The role requires close collaboration with cross-functional teams including R&D, Manufacturing, Regulatory Affairs, Marketing, and Operations.
Senior Validation Engineer Consultant Karwell TechnologiesSenior Validation Engineer ConsultantDevens, MASenior CQV Engineer / Senior Validation Engineer with experience supporting commissioning, qualification, and validation activities for process equipment in GMP-regulated environments. Experience working with bioprocess equipment including bioreactors, filtration systems, chromatography systems, and ultrafiltration (UF) preferred.
Development Engineer II Integrated Resources, IncDevelopment Engineer IILexington, MassachusettsContractorThe Development Engineer / Associate will also analyze experimental data, document results and conclusions in technical reports, and assist Senior Staff with drug product tech transfer management projects. Additional responsibilities will include performing drug product process development studies in collaboration with drug product manufacturing and formulation development teams.
Field Service Engineer II (Medical Devices) - Boston, MA Boston Scientific CorpField Service Engineer II (Medical Devices) - Boston, MABoston, MARequired qualifications: 1 year of experience with an Associate's degree or technical diploma in Electronics, Biomedical Engineering, Life Sciences, or a related technical field; OR an equivalent combination of education, training, and relevant work experience demonstrating the knowledge, skills, and abilities required for the role. The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com-will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role.