NewDirector of Healthcare Facilities Management Macpower Digital Assets Edge Private LimitedDirector of Healthcare Facilities ManagementFramingham, MA$128,000–$175,000 / yearDevelops, implements, administers, and modifies programs to maintain the physical plant, grounds, and equipment through effective utilization of personnel and materials in accordance with local, state, and federal codes, and hospital policies / procedures. Complying with corporate policy and procedures for managing supplies and equipment, promoting teamwork with physicians and all health care providers to maintain internal and external customer satisfaction, and appropriate resource management.
Associate Scientific Strategy Consultant ZifoAssociate Scientific Strategy ConsultantBoston, MARemote$110,000–$125,000The Associate Scientific Strategy Consultant sits within the North American consulting group wherein key accountabilities include driving project elucidation, stakeholder management and defining & driving project success in partnership with internal and external stakeholders. Familiarity with scientific workflows (e.g., bioanalysis, compound management, medicinal chemistry)and key data concepts within the life sciences industry and relevance to operational activities and enabling decision-making.
Java Developer ZifoJava DeveloperBoston, MA$90,000–$110,000The role involves configuring, implementing, and supporting solutions, writing Jira stories, and collaborating with stakeholders to translate business requirements into actionable tasks. Our team’s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 7 of the Top 10 Biopharma companies.
ELN Analyst (Benchling) ZifoELN Analyst (Benchling)Boston, MA$90,000–$125,000The role will partner closely with Customer’s Research and Technical Development scientists to understand their scientific workflows and translate those needs into scalable, consistent Benchling solutions. Demonstrated ability to gather, refine, and translate user requirements into high quality requirements, design, and data model documentation to support scalable implementation and ongoing platform support.
Research Associate - Contract Connexion Systems + EngineeringResearch Associate - ContractBelmont, MAThe primary responsibilities of this role include, but are not limited to: Develop ocular formulations and associated manufacturing processes for pre-clinical and clinical applications. Bachelors degree in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutics, Pharmaceutical Sciences, Biomedical Engineering, or a related scientific discipline.
GxP Lab Computing Analyst ZifoGxP Lab Computing AnalystFramingham, MA$80,000–$90,000Candidate must possess excellent analytical and interpersonal skills along with a proven track record in system design, implementation, have demonstrated ability to guide the activities of colleagues, and have demonstrated ability to gain client’s confidence and trust. The Zifo Lab Computing Analyst provides both consulting, analytical and technical laboratory services, including multivendor instrument, information technology as well as in-lab validation/compliance services when applicable.
Process Development Associate Integrated Resources, IncProcess Development AssociateLexington, MassachusettsContractorBS/MS in degree in chemical, biochemical, biomedical engineering, chemistry or related field • 3-6 years industry experience in formulation and/or drug product process development • Experience in supporting tech transfer projects to contract research and/or manufacturing organizations • Project management experience including time and resource scheduling • Experience in a GMP environment or GLP laboratory is preferred • Experience with Microsoft Project, Vizio, and advanced Excel spreadsheets is preferred • Experience managing outsourced research projects is a plus • Knowledge of statistical design of experiments is a plus. Location- Lexington, MA Duration- 9m +++ Development Engineer / Associate (Contract) – Clinical Drug Product Manufacturing Sciences (CDPMS) The Development Engineer / Associate – CDPMS will assist drug product tech transfer teams with project management support.
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.
Scientist I Nova BiomedicalScientist IWaltham, MA$65,000–$75,000 / yearWith headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we’re building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity. 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.
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.
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.
Automation Engineer - Scientific Data, AI/ML Pipelines & Integration Dev ZifoAutomation Engineer - Scientific Data, AI/ML Pipelines & Integration DevBoston, MA$80,000–$140,000Design and optimize SQL and NoSQL data models and build ETL/ELT and next-generation data pipelines to support structured, semi-structured, and high-volume scientific data, analytics, and AI/ML workloads, including dataset preparation, feature engineering, and model integration into pipelines and applications. Design, develop, and maintain Python-based backend services, APIs, microservices, and data pipelines on AWS using FastAPI and supporting frameworks such as Flask or Django, including integrations with scientific systems such as Benchling, Signals, LIMS, ELN, CDS, and SDMS.
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.
Field Service Engineer Connexion Systems + EngineeringField Service EngineerCanton, MA$70,000–$90,000 / yearAssociates or Bachelors degree in Analytical Chemistry, Engineering, Instrumentation, Biomedical Engineering, or related field (or equivalent experience). Diagnose and troubleshoot hardware, software, and application-related issues on systems from SCIEX, Agilent, Thermo Fisher, Waters, Shimadzu, Bruker, and PerkinElmer.
NewInformation Technology Engineer (Senior Manufacturing Engineer - Medical Device Equipment) Macpower Digital Assets Edge Private LimitedInformation Technology Engineer (Senior Manufacturing Engineer - Medical Device Equipment)Raynham, MA$34 / hourManufacturing and Product Transfer Experience: Must have experience managing manufacturing and product transfers, ensuring smooth and efficient scaling of production processes. Mechanical and Biomedical Engineering Background: Must have a solid background in mechanical, manufacturing, or biomedical engineering to address technical challenges and solutions.
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.
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.
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.
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.
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.