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.
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.
Sr. Scientist - Gene Delivery AstraZeneca PlcSr. Scientist - Gene DeliveryWaltham, MA$116,284–$174,426 / yearEducation and experience: PhD with 0-5 years of post-graduate experience in a relevant field, including but not limited to bioengineering, chemical engineering, biomedical engineering, molecular biology, synthetic biology, biochemistry, and immunology. This is where you'll find newly designed, activity-based workspaces to suit a variety of working styles while increasing collaboration between teams and the greater research community.
Product Engineer - Spinal Implant Development - Newton, MA Michael Page InternationalProduct Engineer - Spinal Implant Development - Newton, MANewton, Massachusetts$90,000–$130,000 / yearFull timeKnown for its collaborative culture, the business works closely with clinical partners and leverages modern manufacturing techniques to bring innovative solutions to market, offering engineers the chance to make a tangible clinical impact. Reporting into the Chief Technology Officer, you will be responsible for the following: Gather, document, and organize surgeon feedback from evaluations, labs, and clinical use of spinal implants and instruments.
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.
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.
Technician, Bioinstrumentation Systems Spear Bio IncTechnician, Bioinstrumentation SystemsWoburn, MADevelop working proficiency in SPEAR assay workflows (sample preparation, plate setup, qPCR readout, SPEARview data analysis) sufficient to troubleshoot workflow failures at customer sites and distinguish instrument issues from assay/reagent issues. Because this role is tightly aligned with engineering, you will be expected to go deeper than a traditional FSE-diagnosing root causes across hardware, software, and assay workflows-and bringing that knowledge directly to customers and back to the team.
NewSoftware Quality Design Engineer Intellectt INCSoftware Quality Design EngineerNULL, MA$38–$435 10 years experience embedded firmware medical devices IEC 62304 / ISO 14971 / ISO 13485 Design Controls SW FMEA Risk Management V&V Jira/ALM/PTC. BS in Engineering, Science, Biomedical Engineering, Software/Computer Engineering, or related technical field + 4 years.
NewSenior Associate Scientist, Upstream Process Development - Bioprocess Automation & Digitization Pfizer IncSenior Associate Scientist, Upstream Process Development - Bioprocess Automation & DigitizationAndover, MA$68,600–$114,300 / yearYou will also be a core contributor to our in-house bioprocess automation and digitization platform - an OPC UA-based system that connects bioreactors, analyzers, and PAT instruments to real-time control logic and data infrastructure across multiple Pfizer development and manufacturing sites. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.
Territory Manager - Lab Automation Flow Control GroupTerritory Manager - Lab AutomationBoston, MAFamiliarity with lab automation workflows such as liquid handling, sample preparation, assay automation, plate handling, thermal control, dispensing, scheduling software, or LIMS/data workflow touchpoints strongly preferred. This is a hands-on, individual contributor sales role responsible for developing new opportunities, expanding existing accounts, and helping customers identify the right automation, workflow, and instrumentation solutions for their lab operations.