Engineering jobs encompass a vast array of specialized roles within the field of engineering, aimed at designing, developing, and maintaining various technological systems and structures. These roles typically require a strong foundation in mathematics and science, and they span across numerous sectors such as civil, mechanical, electrical, and software engineering, among others. The key features of engineering careers include problem-solving, innovation, and the application of practical knowledge to create solutions that can improve people's lives, enhance business operations, or even address global challenges. Engineers often work in teams, collaborate with other professionals, and are at the forefront of technological advancement.
Engineering jobs encompass a variety of roles that involve applying scientific and mathematical principles to solve real-world problems. These positions are typically associated with the design, development, and maintenance of structures, machines, and systems. Engineers are known for their technical expertise, problem-solving skills, and the ability to innovate. Characterized by fields such as civil, mechanical, electrical, chemical, and software engineering, these jobs often require specialized education and can lead to careers in industries like construction, manufacturing, technology, and environmental management. Engineering professionals play a vital role in shaping the future through sustainable and efficient design.
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. I Am Abiomed I Am Heart Recovery Patients First!
The Sr. Electrical Engineer in the Post Market Engineering group plays an integral role in Abiomed's Quality Department, conducting post-market investigations of FDA-approved medical devices. In this position, you will conduct complaint failure investigations and lead CAPAs. This is a position designed to build upon engineering skillset that includes root cause analysis, fixture design, project management, medical
device knowledge, and cardiology clinical background. Principle Duties and Responsibilities: • Function as the lead complaint investigator. Investigate complaints by reviewing clinical notes, analyzing medical device data, and by troubleshooting returned products to determine a root cause • Serve as a subject matter expert for durable products and their associated failure modes • Identify optimal analytical approaches critical to problems by mitigating/ resolving failures to improve product quality and reliability • Develop root cause failure analysis techniques to automate processes and testing methods • Apply statistical tools to analyze data and drive problem resolution • Drive corrective
and preventive actions in a timely manner to prevent the re-occurrence of problems • Lead engineering projects through design changes (HW/SW), which includes modifying schematics, PCB layouts, and other engineering models • Run small projects by developing a project plan and adhering to design controls• BS in Electrical Engineering, Biomedical Engineering, or directly related scientific discipline required.
MS desired • Minimum of 4 years of related work experience • Experience interpreting circuit schematics, BOMs, and technical drawings • Knowledge of electrical design software tools (Schematic capture and PCB layout) • Ability to communicate ideas and information clearly, effectively, and frequently (oral and written) • Determination to overcome obstacles and the initiative to execute tasks in a timely manner without direct supervision • 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 Preferred Qualifications • Project lead experience is a plus • Medical device and electromechanical design experience preferred • Ability to troubleshoot electronics down to component-level • Experience with programming languages such as C/C , Python, Matlab, and SQL • Knowledge of electronics manufacturing and ability to interface with suppliers • Experience with fiberoptics and digital communication protocols • Cross-functional experience with hardware/ software and analog/ digital systems Abiomed is an Equal Opportunity Employer committed to a diverse workforce.
Abiomed will not discriminate against any worker or job applicant on the basis of race, color, religion, gender, gender identity, national origin, ancestry, age, interactionual orientation, gender identity, marital or civil partnership status, pregnancy, gender reassignment, non-job related mental or physical disability, genetic information, veteran status, military service, application for military service, or membership in any other category protected under law.
Abiomed maintains a drug-free workplace.
respiratory support, with a mission of recovering hearts & saving lives. Abiomed's " Patients First! " 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. This role reports directly to the Director, Post Market Surveillance and engages in all activities related to the Abiomed post market surveillance processes. This role will help manage annual reports, track and trend complaint data, enable
signal detection, and escalate trends or issues as needed in accordance with procedural guidance. This individual will present post market data in any forums as necessary (data review board, complaint trending meetings, etc.
) This role will also provide support during inspections by regulatory bodies and ensure appropriate post market surveillance information is available and fit for delivery to the front room. Responsibilities : • Subject matter expert accountable for Abiomed Post Market Surveillance (PMS) activities including leading discussions and presenting PMS data in any required forums. • Develops and presents post market surveillance data for management review. • Participates
in cross-functional and global teams developing and managing post market surveillance activities.
• Collaborates with key business partners to develop and implement effective data analysis associated with post-launch monitoring of product performance in the field. Explores and investigates relationships between key risk factors, medication, and procedural information and adverse events/complaint rates. • Collaborates with business partners to develop informative annual reports and other post market surveillance activities when such activities are required as part of the post market surveillance commitments. • Keeps abreast of current trends in literature and research pertaining to data analysis for complaints / adverse event data.
• Ensures compliance with QSR, MDV, MDR, MPR, and any applicable country regulations and requirements regarding post market surveillance trending. • Support additional information requests from global regulatory agencies. • Working knowledge of FDA Medical Device Regulations including Quality System Regulation 21 CFR Part 820, and applicable international quality standards including ISO 13485:2013, Canadian MDR, EU MDR and country specific vigilance related regulations. • Strong analytical skills including trend and statistical analysis, interpersonal, and management skills.
• Perform other duties as required. Education: • BS degree with at least 5 years' experience in medical devices specifically related to post market surveillance Requirements: • Experience with FDA audits in both a front and backroom capacity is preferred • Statistical knowledge and understanding • Ability to travel 10% domestically and internationally • Demonstrated successful project management preferred • Strong leadership skills to inspire high quality, timely work, and instill a spirit of continuous improvement • Strong knowledge and experience in quality management of medical devices to maintain compliance with 21 CFR 820, 21 CFR 806, ISO 13485 & 14971, EU MDR • Demonstrated ability to implement and maintain accurate documentation consistent with applicable quality standards • Must be able to work independently, and demonstrate a high level of reliability, integrity, and personal accountability • Must have excellent written and verbal communication skills and have a strong working knowledge of the development, application, and measurement of quality performance metrics For U.
S. applicants, in accordance with applicable disclosure requirements, the anticipated base pay range for this position is $125,000 to $165,000.
Additional information can be found through the link below. For additional general information on company benefits, please go to: www. careers. /employee-benefits 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.
and able to work in a multi-disciplined development team. This position is based in Danvers, MA. KEY RESPONSIBILITIES Participate in the development of electronic medical devices including system architecture, detailed circuit design / implementation and software for embedded systems Act as a technical lead for legacy product improvement Hands-on circuit design, schematics and PCB layouts, and board bring-up Fabricate PCBAs for Automated Impella Controller working with internal technical team and board fab vendor Test and troubleshoot PCBAs of existing and new products to the component level to address design related issues Work with internal and external manufacturing partners to ensure
producible designs (DFx) Support the development of test methods and conduct characterization of engineering prototypes QUALIFICATIONS BS in Electronic Engineering, MS Preferred Minimum of 4 years of related work experience desired integration of custom circuitry with embedded PC systems and subcomponents as well as DSP Hands-on electrical circuit design experience of analog, digital, and mixed signal systems Understanding of signal processing, sensors, and motor driver systems Expertise with electrical design software tools (Schematic capture and PCB layout Fundamental understanding of 60601-1 standards Ability to communicate ideas and information clearly, effectively, and frequently
(oral and written) Must be proficient in Microsoft Office Suite May require up to 10% travel - US & EU Preferred: Medical Device Experience Software development skills - Knowledge of Real Time OS such as QNX or Linux and programming languages such as C, C , or Python.
Altium experience strongly preferred Working knowledge of SAP 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..
development team. The position is based in Danvers, MA. KEY RESPONSIBILITIES • Participate in the development of electronic medical devices including system architecture, detailed circuit design / implementation and software for embedded systems • Act as a technical lead for legacy product improvement: h ands-on circuit design, schematics and PCB layouts, and board bring-up • Fabricate PCBAs working with internal technical team and board fab vendors • Test and troubleshoot PCBAs of existing and new products to the component level to address design related issues • Work with internal and external manufacturing partners to ensure producible designs (DFx) • Support the development of test methods
and conduct characterization of engineering prototypes QUALIFICATIONS • BS in Electronic Engineering, MS Preferred • Minimum of 6 years of related work experience desired • Integration of custom circuitry with embedded PC systems and subcomponents as well as DSP • Hands-on electrical circuit design experience of analog, digital, and mixed signal systems • Understanding of signal processing, sensors, and motor driver systems • Expertise with electrical design software tools (Schematic capture and PCB layout) • Ability to communicate ideas and information clearly, effectively, and frequently (oral and written) • Must be proficient in Microsoft Office Suite • English Required • May require up to
10% travel - US & EU Preferred: • Medical Device Experience • Software development skills - Knowledge of Real Time OS such as QNX or Linux and programming languages such as C, C , or Python.
• Altium experience strongly preferred • Working knowledge of SAP 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..
verification test plan and protocols. KEY RESPONSIBILITIES Understand device design and core technologies in order to inform test method development Review, update, understand and determining the scope of testing required Develop test methodologies within framework of SOP's and FDA guidelines Create verification and validation test plans Write concise and effective test protocols Informal and formal test execution of verification and validation protocols Produce test reports, document test results, maintain records and assure traceability Creating and evaluating test fixtures needed for product design verification Contributing to design failure investigations that may impact Risk backssment,
Hazard Analysis, and FTA's QUALIFICATIONS BS or MS in Electrical Engineering, Mechanical, Software Engineering, Biomedical Engineering or related field required Minimum of 2 years of Verification & Validation experience Medical Device Experience Fundamental understanding of 60601-1 standards May require up to 5% travel - US & EU Preferred: Prior experience in embedded device testing Fundamental understanding of design controls Familiarity with JAMA requirements management software 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..
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..
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..
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..
and driven individual to own and collaborate on engineering design initiatives. You will have a tangible impact on this new platform, the business, and ultimately improving patient care. As a Product Development Engineer II, you will make significant contributions to innovative technologies in Abiomed's pre CARDIA platform to address acute decompensated heart failure.
The role is responsible for key engineering project deliverables around our next generation console and catheter. This technical engineer will lead complex technical design and development tasked activities, collaborate with senior and junior staff to execute tasks, and coordinate with cross-functional teams to achieve success.
Principal Duties and Responsibilities: Provide product development expertise leading system design and engineering initiatives Execute across a diverse group of engineering disciplines (mechanical, human factors, systems, and test) Establish design goals and specifications based on voice of customer and requirements Effectively engage with a cross-functional team to address complex product development challenges and drive toward robust solutions Apply and/or develop highly advanced technologies, scientific principles, theories, and concepts that may be new to the industry Recognize the gaps, initiate, develop, and establish infrastructure, tools, and knowledge base to propel successful
product developments Build breadboards, test concepts, and iterate quickly to reach milestones Generate 3D CAD models and engineering drawings in Solidworks using GD&T with ability to write specifications and to perform tolerance stack-up analyses.
Committed to being customer focused and responsive to unmet needs Job Qualifications: Bachelor's degree in a scientific or engineering discipline (Mechanical background desired); Advanced degree preferred Proficient in 3D CAD (Solidworks), DFM (design for manufacturing), and material selection. Ideal candidate will have experience (from concept to commercial) engineering catheters 4 years leading and executing successful Product Development projects, providing hands on technical management, preferably in medical devices.
Knowledge of cath lab and/or cardiothoracic/vascular surgical environments is a plus. Experience throughout product development, including requirement definition, Human Factors (IEC 62366), design characterization, and transfer to manufacturing History of applying fundamental concepts of mechanical design and material properties to drive product development Ability to communicate ideas and information clearly, effectively, and frequently (oral and written) Strong problem-solving skills and experience identifying root cause Execution driven, highly adaptable, thrives in a rapid paced, complex environment Able to travel 10% of time within the US and Overseas 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..
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. I Am Abiomed I Am Heart Recovery Patients First!
ABIOMED is redefining team-driven success while reshaping heart recovery. Here, new ideas are welcomed and encouraged, learning is constant, and our dynamic setting enables positive people to do profoundly important work. The Senior Supplier Quality Engineer serves as ABIOMED's primary technical contact with all US based suppliers, leads all product development team's supplier initiatives, second source critical
suppliers, and establishes " Quality at the Source" programs with key partners. This role is a key technical resource for the company's continued growth, and is a great opportunity for someone to make a difference at one of the fastest-growing medical technology companies, focused on recovering hearts and saving lives.
The role is responsible for evaluating, monitoring, and improving the quality of products and services delivered by external suppliers. This role involves working closely with suppliers, cross-functional teams, and internal quality departments to maintain high standards of product quality, safety, and regulatory compliance Key Responsibilities: Supplier backssment:
backss and qualify new suppliers by evaluating their capabilities, quality control processes, and compliance with quality standards and regulatory requirements.
Quality Standards: Develop and maintain supplier quality standards, specifications, and inspection criteria. Ensure suppliers adhere to these standards. Quality Audits: Participate in supplier audits activities to monitor their quality processes, identify non-conformances, and drive corrective and preventive actions. Supplier Performance: Monitor and report on supplier performance metrics, such as defect rates, on-time delivery, and quality improvement initiatives. Root Cause Analysis: Investigate and analyze quality issues and non-conformances, working with suppliers to identify root causes and implement corrective actions.
Quality Improvement: Collaborate with suppliers to implement quality improvement plans, including process changes, quality control methods, and continuous improvement initiatives. Regulatory Compliance: Ensure suppliers meet all relevant regulatory and industry quality standards and requirements, particularly in regulated industries (e. g. medical devices, aerospace). Risk Management: Identify and mitigate quality and supply chain risks associated with supplier activities.
Collaboration: Work closely with internal departments such as procurement, engineering, manufacturing, and quality assurance to ensure alignment and effective communication with suppliers. Documentation: Maintain accurate and up-to-date records of supplier quality activities, audits, and quality agreements. Training: Provide training and support to suppliers in quality management and process improvement. Cost Management: Collaborate with suppliers to identify cost-effective quality improvement solutions and cost reduction initiatives. Required: Bachelor's degree or equivalent experience in engineering or a related field.
Minimum 4 years of professional engineering experience. Demonstrated ability in supplier quality engineering, quality control, or a related role. In-depth knowledge of quality management systems and standards (e. g. ISO 9001). Strong understanding of statistical analysis and quality improvement methodologies (e. g. Six Sigma). Experience with supplier audit processes and tools. Excellent problem-solving and root cause analysis skills. Strong communication skills. Strong interpersonal and teamwork skills. Ability to work in a multi-functional and diverse team environment.
Strong organizational and time management skills. Preferred: Master's of Science in Manufacturing Engineering, Mechanical Engineering, Material Science, or related science/engineering field Excellent technical communication and interpersonal skills Experience working in a multi-functional environment and partnering with design teams on new product development. Expertise with statistical analysis techniques (process DOE, process validation/ stability/control/capability) and qualifying component manufacturing processes Experience in a regulated industry with the associated manufacturing environment and design control requirements Highly organized and creative, with strong analytical, problem-solving, and conflict analysis/resolution skills 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.
Engineering jobs encompass a broad range of professions that involve the application of science and mathematics to solve problems and design, construct, and maintain structures, devices, and systems. These jobs are characterized by creativity, analytical skills, and the pursuit of technological innovation. Engineers can specialize in various fields, such as civil, mechanical, electrical, software, or biomedical engineering, each with its distinctive focus and techniques. A hallmark of engineering roles is their impact on shaping our built environment and the way we interact with technology, making them crucial for the advancement and sustainability of modern societies.
Engineering jobs encompass a broad range of professions that involve the application of science and mathematics to solve problems and design, construct, and maintain structures, devices, and systems. These jobs are characterized by creativity, analytical skills, and the pursuit of technological innovation. Engineers can specialize in various fields, such as civil, mechanical, electrical, software, or biomedical engineering, each with its distinctive focus and techniques. A hallmark of engineering roles is their impact on shaping our built environment and the way we interact with technology, making them crucial for the advancement and sustainability of modern societies.
