Boston Field Service Technician Wright Technical ServicesBoston Field Service TechnicianBoston, MAPerform performance assurance (PA) inspections, scheduled maintenance, electrical safety inspections (ESI), and operation verification procedures (OVP) on highly complex and intricate biomedical equipment and systems. For individuals who take pride in precision, problem-solving, autonomy, and professionalism, this career offers continuous learning, growing responsibility, and a clear path to leadership within a rapidly expanding, employee-owned company.
Biprocess Engineer Integrated Resources, IncBiprocess EngineerDevens, MassachusettsContractorPreferred: Prior experience scaling up biopharma manufacturing processes (upstream/downstream), facility fit assessments, process scale-up from bench/ pilot to production, process troubleshooting and optimization, and process validation. The successful candidate will work effectively in highly cross-functional project teams, matrix management environments, as well as independent working environments to support the site.
Process Engineer - Upstream/Downstream Integrated Resources, IncProcess Engineer - Upstream/DownstreamDevens, MassachusettsContractorPreferred: Prior experience scaling up biopharma manufacturing processes (upstream/downstream), facility fit assessments, process scale-up from bench/pilot to production, process troubleshooting and optimization, and process validation. The successful candidate will work effectively in highly cross-functional project teams, matrix management environments, as well as independent working environments to support the site.
Software Architect - EP 3D Mapping Systems - Boston Area Michael Page InternationalSoftware Architect - EP 3D Mapping Systems - Boston AreaMarlborough, Massachusetts$160,000–$200,000 / yearFull timeThis role requires a hands-on technical leader capable of defining software architectures, contributing directly to development branches, guiding technical execution across engineering teams, and translating clinical workflow needs into robust software solutions. The key responsibilities for the Software Architect of Electrophysiology Navigation & Mapping Systems will include but are not limited to: Serve as the software architecture lead for next-generation electrophysiology navigation and mapping initiatives.
Senior Plastics Process Engineer Nova BiomedicalSenior Plastics Process EngineerBillerica, MA$130,000–$145,000 / yearPlastics Processing Engineer, you will have guidance and oversight on daily operations within the mold shop including supporting production schedules, maintaining equipment within the department, establishing molding process parameters, executing mold process validations, and resolving molding issues. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences.
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.
Senior Design Quality Engineer Karwell TechnologiesSenior Design Quality EngineerAndover, MAAs a Senior Design Quality Engineer (DQE) for our medical device manufacturer client in the Greater Boston region, you will be responsible for ensuring end-to-end design quality and compliance across the product development lifecycle for Class II/III medical devices, including software-driven and active implantable products. In this role you will play a key role in: Serving as the quality lead on product development teams, ensuring compliance with design controls across all lifecycle phases (planning, inputs/outputs, verification, validation, transfer, and change management).
Design Quality Engineer Karwell TechnologiesDesign Quality EngineerAndover, MAAs a Design Quality Engineer (DQE) for our medical device manufacturer client in the Greater Boston region, you will be responsible for ensuring end to end design quality and compliance across the product development lifecycle for Class II/III medical devices, including software-driven and active implantable products. At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world's most innovative companies unleash their potential.
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.
Database Engineer Integrated Resources, IncDatabase EngineerWestborough, MassachusettsFull timeRole Summary: A development engineer 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.
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.
Senior Design Quality Engineer Katalyst Healthcares & Life SciencesSenior Design Quality EngineerAndover, MAAs a Senior Design Quality Engineer (DQE) for our medical device manufacturer client in the Greater Boston region, you will be responsible for ensuring end-to-end design quality and compliance across the product development lifecycle for Class II/III medical devices, including software-driven and active implantable products. In this role you will play a key role in: Serving as the quality lead on product development teams, ensuring compliance with design controls across all lifecycle phases (planning, inputs/outputs, verification, validation, transfer, and change management).
Design Quality Engineer Katalyst Healthcares & Life SciencesDesign Quality EngineerAndover, MAAs a Design Quality Engineer (DQE) for our medical device manufacturer client in the Greater Boston region, you will be responsible for ensuring endtoend design quality and compliance across the product development lifecycle for Class II/III medical devices, including software-driven and active implantable products. At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world's most innovative companies unleash their potential.
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.
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.
Sr. Development Quality Engineer LancesoftSr. Development Quality EngineerWestford, MA$43.33CAPA management including (but not limited to) performing thorough investigations with detailed root-cause analyses with established methods (Fishbone, 5 Why), implementing corrections, corrective actions, creating and monitoring effectiveness criteria. Education And Experience You ll BringBachelor level degree in Computer science, biomedical engineering, software engineering or a closely related discipline or an equivalent combination of education and work experience.
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 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.
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.