Free Classified Ads in Peabody, MA

solutions, design & develop capable and scalable manufacturing processes. You will work in a dynamic fast paced environment that is disrupting the medical device industry by bringing breakthrough technologies to market. The ideal candidate brings deep experience in product design and manufacturing of medical devices.

This role focuses on the Impella ECP™ or " Expandable Cardiac Power" The Impella ECP™ is Abiomed's smallest heart pump that does not compromise on flow by utilizing unique expanding pump technology. Principle Duties and Responsibilities may include: Lead early-stage design & process development projects of novel hemodynamic support devices and accessories. Provide

guidance and mentorship to engineering teams. Lead initiatives with engineers in research, product development, new product introduction and contract manufacturers or OEMs.

Design and develop electromechanical systems and components for medical devices, with a focus on fiber optics, motors, drive shafts, bearings, PCBs, fixtures, automation, and CAD. Serve as Subject Matter Expert (SME) across platforms and lifecycle phases from research through sustaining teams Represent Abiomed to physicians, industry groups, and technical partners. Conduct voice of the customer and transform clinical observations into new device concepts and requirements Generate intellectual property through

invention disclosures in pursuit of patients and trade secrets.

Turn concepts into reality by rapidly prototyping using a variety of fabrication techniques. Test and iterate on your designs to develop an optimal solution. Bring solutions to market by collaborating with an exceptional cross-functional team. Conceptualize, design, prototype, procure, and build components and assemblies for products and testing/manufacturing equipment and fixtures. Lead the planning and execution of animal and cadaver labs throughout the development cycle. Conduct feasibility testing, analyze, and report on test results providing conclusions and recommendations. Perform failure investigations in the event of test failures with support from the technical team.

Job Qualifications: BS or MS in Electrical Engineering, Mechanical Engineering or directly related field. 12 years of related experience in medical device, 8 years in product development. Strong problem-solving skills and demonstrated experience identifying root cause of device failures. Demonstrated ability to execute tasks in a timely manner under minimal supervision. Willingness to learn the interventional cardiology space - the devices and the clinical practice. Experience applying statistical techniques and analysis.

Willingness & ability to travel internationally ~5% of the time. Strongly Preferred Qualifications: Experience in FDA Class II and III medical devices. Experience in Solidworks 3D modeling, 2D drawing applying GD&T. Able to model complex parts and assemblies and conduct basic structural and fluid FEA. Proficiency in fiber optic systems, motors, PCB's, signal processing Hands on experience in prototyping in pilot manufacturing and rapid prototyping; basic machine shop equipment Hands on experience in testing in a laboratory environment Strong understanding of design control and risk management processes and deliverables Strong understanding of statistical analysis of data Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.

All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www. careers..

Support technical efforts amongst senior engineers, test engineers, designers, technical writers, and technicians in the execution of project deliverables. • Conceptualize, design, procure, and build components and assemblies for products and testing/manufacturing fixtures.

• Support the planning and execution of animal and cadaver labs throughout the development cycle. • Conduct feasibility/verification testing, analyze, and report on test results providing conclusions and recommendations. Perform failure investigations in the event of test failures with support from the technical team. • Lead subproject technical initiatives at contract manufacturers or OEMs. Coordinate vendor deliverables,

track progress, and communicate status to project team. • Draft design control deliverables including design inputs/outputs and verification/validation efforts with the support of senior engineers.

• Support the generation of risk documentation including d FMEA, u FMEA, p FMEA, hazard analysis, and risk management plans/report with the support of senior engineers. • Author test plans, protocols, and summary reports following completion of formal testing. • Comply with documentation requirements of design control defined by ISO 13485. Required Qualifications: • BS in Mechanical, Biomedical Engineering or directly related scientific discipline. • 2 years of medical device engineering or

product development experience • Strong problem-solving skills and demonstrated experience identifying root cause of device failures.

• Demonstrated ability to execute tasks in a timely manner under minimal supervision. • Willingness to learn the interventional cardiology space - the devices and the clinical practice. • Experience applying statistical techniques and analysis in industry or education. • Willingness & ability to travel internationally ~5% of the time. Strongly Preferred Qualifications: • 2 years of medical device engineering or product development experience preferred. • Manufacturing/Prototyping and hands-on experience preferred. • 3D modeling and 2D drawing experience preferred.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www. careers..

" culture drives our skilled workforce and strong relationships with clinicians. Our innovative product portfolio and robust pipeline provide us the incredible opportunity to bring lifesaving technology to more patients around the world than ever before.

Founded in 1981, Abiomed has a proven track record for growth, integrity and innovation. As an Engineer II you will execute testing in support of product development and work alongside the team to solve complex technical problems. This position will focus on supporting the development of the next generation of hemodynamic support devices. The ideal candidate will be hands-on, data-driven, detail oriented and ready to thrive in fast

paced innovative environment. Principle Duties and Responsibilities may include : Plan, execute, and document feasibility and verification testing in support of product development Lead the design verification phase of product development to include writing plans/protocols/reports, coordinating logistics, and leading phase reviews Develop new testing techniques on novel hemodynamic support devices and their accessories from concept through test method validation Draft feasibility engineering summaries as well as verification test plans, protocols, and reports.

Analyze data and interpret test results. Design and update test fixtures and all associated documentation, including CAD

models, drawings, and article specifications. Conduct fixture qualification.

Coordinate and participate in testing efforts alongside testing technicians, technical writers, and technicians in the execution of project deliverables. Collaborate as part of cross-functional project teams including product development, quality, regulatory, and manufacturing. Coordinate with outside vendors who are fabricating or calibrating testing fixtures Job Qualifications: BS in Mechanical, Electrical, or Biomedical Engineering or related degree 4 years of medical device engineering or test engineering experience Expertise working with basic lab & test equipment, e. g. multimeter, microscope, pressure sensor, thermocouple, etc.

required. Experience testing with animal blood and flow loops preferred Ability to effectively lead small cross-functional teams to solve technical and logistical challenges. 3D modeling and 2D drawing experience required. Solidworks preferred. Experience applying statistical techniques and analysis. Proficient in English verbal and written communication. A passion for medical devices and making a significant positive impact on the lives of our patients May require up to 10% travel - US & EU Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.

All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www. careers..

product introduction and contract manufacturers or OEMs. Collaborate to deliver designs with margin to performance requirements and demonstrated process capability in scalable manufacturing processes. Serve as Subject Matter Expert (SME) across platforms and lifecycle phases from research through sustaining teams Conduct voice of the customer and transform clinical observations into new device concepts and requirements Generate intellectual property through invention disclosures in pursuit of patients and trade secrets.

Turn concepts into reality by rapidly prototyping using a variety of fabrication techniques. Test and iterate on your designs to develop an optimal solution. Bring

solutions to market by collaborating with an exceptional cross-functional team. Conceptualize, design, prototype, procure, and build components and assemblies for products and testing/manufacturing fixtures.

Lead the planning and execution of animal and cadaver labs throughout the development cycle. Conduct feasibility testing, analyze, and report on test results providing conclusions and recommendations. Perform failure investigations in the event of test failures with support from the technical team. Required Qualifications: BS in Mechanical Engineering or directly related scientific discipline. 6-8 years of related experience in medical device, 3 years in manufacturing or new

product introduction. Strong problem-solving skills and demonstrated experience identifying root cause of device failures.

Demonstrated ability to execute tasks in a timely manner under minimal supervision. Willingness to learn the interventional cardiology space - the devices and the clinical practice. Experience applying statistical techniques and analysis. Willingness & ability to travel internationally ~5% of the time. Strongly Preferred Qualifications : Experience in FDA Class II and III medical devices. Experience in Solidworks 3D modeling, 2D drawing applying GD&T, PDM. Able to model complex parts and assemblies and conduct basic structural and fluid FEA.

Proficiency in scientific molding and other plastic processes including insert molding and complex engineered shafts Proficiency in laser-cutting, machining, coatings and finishing of metals and ceramics. Experience in equipment and tooling design, fabrication, process development, and validation. Hands on experience in prototyping in pilot manufacturing and rapid prototyping; basic machine shop equipment Hands on experience in testing in a laboratory environment Strong understanding of design control and risk management processes and deliverables Experience in design for manufacturing of plastic and metal components Strong understanding of statistical analysis of data, DOE's, DMAIC, DFSS, Six Sigma Green Belt Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.

All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www. careers..