Dfx engineering intern Job at Axon (Scottsdale)

Eng Ii, Systems

The role of Engineer II , Product Owner is to contribute in design and developme...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Mechanical engineering, Electrical Engineering, Electronics Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field
3 to 6 yrs of experience, mainly in System engineering function of Electro-Mechanical System Design
Experience in Medical Device development, FDA Regulations and MDR
Exposure to Usability Engineering Process
Experience in QFD, Pugh Matrix, CTQ, DFR, DFX
Strong interpersonal skills with the ability to collaborate with others in a team environment
Understanding of and adherence to FDA, ISO and IEC design control procedures, regulations and standards
Demonstrated experience in accomplishing objectives. Able to deliver on multiple projects simultaneously
Self-motivated with good interpersonal skills

Job Responsibility

Identify and define internal and external customer needs, functions, performance, usability and safety requirement for product or solution with thorough knowledge and understanding constraints - Business and Regulatory, Design trade-offs and Risk assessment early in the development cycle working independently or under the guidance of senior staff
Provide your technical expertise to ensure that the project successfully meets cost, quality and schedule targets throughout the product life cycle
Excels in the development of Use Case for product or solution based on intimate knowledge of customers and their environments
Use tools such as DOORS, POLARION or equivalent and excels in the management of requirements and decomposition of system level requirements to modules
Carry out risk management process in accordance with the EN ISO 14971 throughout product life cycle to ensure compliance and product safety
Identify development issues and facilitates in the resolution using optimal technology solutions
Supports in the Usability Engineering activities to ensure the application of human factor in the development of products or solutions to demonstrate compliance to IEC 62366 and FDA guidance
Knowledge in the application of principles of Reliability and Robustness in the development of products or solutions
Completes detailed, high quality technical documentation to capture and communicate designs
Support integration issues during development tests and ensure module / system development is successful

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Dfx Engineer

Meta is at the forefront of developing innovative hardware that redefines how pe...

Location

United States , Sunnyvale

Salary:

173000.00 - 245000.00 USD / Year

Senior NPI Engineer

The NPI Engineer is responsible for shepherding hardware from concept review to ...

Location

United States , Bozeman

Salary:

115000.00 - 184000.00 USD / Year

Aurora Innovation

Expiration Date

Until further notice

Requirements

Minimum of 8 years experience in engineering role with experience working in low to high volume production environments.
Experience with launching hardware products and the product life cycle, and selecting the right-sized process based on the needs of the program.
Experience in relevant fields – optical alignment process development, optical interconnect, chip-to-chip coupling, and FAU alignment
Participate in the process of bringing up a new technology from the R&D stage to high volume manufacturing.
Proficient in SPC, 6 sigma, quality control process
good understanding of machine and process interactions.
We are seeking applicants who demonstrate the ability to work independently, deliver results promptly, communicate effectively, operate with a sense of urgency, and thrive in a fast-paced development and production environment.
Experience with working with supply chain and vendors, bonus points for experience in design engineering and new product introduction.
Working knowledge of GD&T.
Experience with 3D CAD and PDM/PLM, preferably Catia/Solidworks and Enovia/EPDM.

Job Responsibility

Support transition of critical automated mirco-optical alignment from engineering to high volume manufacturing at CM.
Ensure end-to-end assembly process readiness for complex lidar systems at manufacturing partners.
Yield analysis monitoring and drive continuous improvement initiatives for NPI production lines, ensure optimal yield and efficiency to achieve capacity and cost target.
Maintain products’ quality by improving design and manufacturing process as well as equipment stability.
Provide onsite engineering support: technical ownership and support for process or equipment issues.
Provide feedback on manufacturing and service requirements, process control plans, and quality assurance. Develop hardware standards and design guidelines.
Own control plans, manufacturing BOM, and necessary documentation to transfer HW from design to the production floor, whether internal or external.
Review data packages before they are released for manufacturing.
Create and maintain work instructions, standard operating procedures, forms, records, checklists, process sequence/routing, Process Flow Diagrams (PFD), PFMEAs, and other required manufacturing documentation
Support and guide the manufacturing team through all phases of Advanced Product Quality Planning (APQP)

What we offer

Annual bonus
Equity compensation

Fulltime

Engineer II, Systems C&S

This is where new knowledge is discovered. Baxter's Research and Development tea...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Mechanical engineering, Electrical Engineering, Electronics Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field
3 to 8 yrs of experience, mainly in Codes and Standards, testing & System engineering function of Electro-Mechanical System Design
Experience in Medical Device development, FDA Regulations and MDR
Exposure to Usability Engineering Process
Experience in QFD, Pugh Matrix, CTQ, DFR, DFX
Strong interpersonal skills with the ability to collaborate with others in a team environment
Understanding of and adherence to FDA, ISO and IEC design control procedures, regulations and standards
Excellence in Medical Devices safety (IEC 60601-1 and collaterals for medical devices like cardiology, patient monitoring and respiratory therapies), FDA Regulations or other applicable regulatory requirements
Excellence in Medical Device software life cycle processes (IEC 62304), EMI/ EMC requirements, REACH, ROHS and Biocompatibility
Demonstrated experience in accomplishing objectives. Able to deliver on multiple projects simultaneously

Job Responsibility

Identify and define internal and external customer needs, functions, performance, usability and safety requirement for product or solution with thorough knowledge and understanding constraints - Business and Regulatory, C&S assessment early in the development cycle working independently or under the guidance of senior staff
Execute compliance testing as a part of the development team to ensure that the project successfully meets cost, quality and schedule targets throughout the product life cycle
Use tools such as DOORS and excels in the management of requirements and decomposition of system level requirements to modules and their respective compliance requirements
Carry out risk management process in accordance with the EN ISO 14971 throughout product life cycle to ensure compliance and product safety
Excels in the application of principles of Reliability and Robustness in the development of products or solution
Completes detailed, high quality technical documentation to capture and communicate designs
As Lead integrator for the product proactively look out for integration issues during development tests and ensure module / system development is successful
Lead the effort in complying with IEC 60601-1 and collateral standards to obtain product approvals from external safety test labs and notified bodies (DQS, UL, ETL, TUV, LNE, etc.)
Excels in obtaining and maintaining 3rd party Product Certifications, Type approvals and technical files
Actively engage with verification and validation engineers to aid in the development of verification scripts with good test coverage

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Manufacturing Technical Manager

In this role, you will be the Operations’ technical owner responsible for end-to...

Location

United States , Sunnyvale

Salary:

144000.00 - 204000.00 USD / Year

Eng II, Systems

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Mechanical engineering, Electrical Engineering, Electronics Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field
3 to 6 yrs of experience, mainly in System engineering function of Electro-Mechanical System Design
Experience in Medical Device development, FDA Regulations and MDR
Exposure to Usability Engineering Process
Experience in QFD, Pugh Matrix, CTQ, DFR, DFX
Strong interpersonal skills with the ability to collaborate with others in a team environment
Understanding of and adherence to FDA, ISO and IEC design control procedures, regulations and standards
Demonstrated experience in accomplishing objectives
Able to deliver on multiple projects simultaneously
Self-motivated with good interpersonal skills

Job Responsibility

Identify and define internal and external customer needs, functions, performance, usability and safety requirement for product or solution with thorough knowledge and understanding constraints - Business and Regulatory, Design trade-offs and Risk assessment early in the development cycle working independently or under the guidance of senior staff
Provide your technical expertise to ensure that the project successfully meets cost, quality and schedule targets throughout the product life cycle
Excels in the development of Use Case for product or solution based on intimate knowledge of customers and their environments
Use tools such as DOORS, POLARION or equivalent and excels in the management of requirements and decomposition of system level requirements to modules
Carry out risk management process in accordance with the EN ISO 14971 throughout product life cycle to ensure compliance and product safety
Identify development issues and facilitates in the resolution using optimal technology solutions
Supports in the Usability Engineering activities to ensure the application of human factor in the development of products or solutions to demonstrate compliance to IEC 62366 and FDA guidance
Knowledge in the application of principles of Reliability and Robustness in the development of products or solutions
Completes detailed, high quality technical documentation to capture and communicate designs
Support integration issues during development tests and ensure module / system development is successful

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Spec, Quality Supplier

This is where you make a difference in our patients’ safety. As a member of the ...

Location

Mexico , Monterrey

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's degree in engineering or related technical field required
Minimum of 3–5 years of experience in supplier quality, manufacturing, or quality engineering within a regulated industry (medical device preferred)
Strong analytical and problem-solving skills, including structured methodologies (e.g., root cause analysis, risk assessment)
Validated background in managing supplier quality, conducting audits, and ensuring regulatory compliance
Effective communication and influencing skills, with the ability to collaborate across all interpersonal levels and with external partners
Proven track record to lead multiple priorities and get results in a sophisticated, regulated environment
Knowledge of manufacturing processes, supplier development, and quality systems
High level of accountability, integrity, and commitment to quality and compliance

Job Responsibility

Lead resolution of supplier-related quality issues, including audit findings and systemic nonconformances (SCARs), ensuring detailed identification of underlying problems and effective corrective actions
Review, evaluate, and approve supplier change requests (e.g., process changes, site transfers), ensuring risks are accurately assessed and mitigated
Build and apply supplier risk management strategies, ensuring continuity of supply and compliance with regulatory and quality requirements
Establish and maintain positive relationships with key suppliers, driving continuous improvement in quality, delivery, and performance
Serve as the Supplier Quality representative during internal and external audits, ensuring supplier-related compliance readiness and effective audit outcomes
Develop, implement, and maintain the Supplier Audit Program, including planning, conducting, and follow-up of supplier audits
Monitor, analyze, and handle supplier performance metrics (scorecards), driving accountability and improvement actions
Support qualification and validation activities for supplier-related changes, including part qualification and engineering change management
Lead structured problem-solving initiatives targeting critical supplier quality issues (e.g., Top Supplier Issues), ensuring sustainable solutions
Provide quality input and insights for Supplier Business Reviews and participate in governance forums related to Supplier Quality Assurance

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Eng II, Systems

This is where new knowledge is discovered. Baxter's Research and Development tea...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Mechanical engineering, Electrical Engineering, Electronics Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field
3 to 6 yrs of experience, mainly in System engineering function of Electro-Mechanical System Design
Experience in Medical Device development, FDA Regulations and MDR
Exposure to Usability Engineering Process
Experience in QFD, Pugh Matrix, CTQ, DFR, DFX
Strong interpersonal skills with the ability to collaborate with others in a team environment
Understanding of and adherence to FDA, ISO and IEC design control procedures, regulations and standards
Demonstrated experience in accomplishing objectives
Able to deliver on multiple projects simultaneously
Self-motivated with good interpersonal skills

Job Responsibility

Identify and define internal and external customer needs, functions, performance, usability and safety requirement for product or solution with thorough knowledge and understanding constraints - Business and Regulatory, Design trade-offs and Risk assessment early in the development cycle working independently or under the guidance of senior staff
Provide your technical expertise to ensure that the project successfully meets cost, quality and schedule targets throughout the product life cycle
Excels in the development of Use Case for product or solution based on intimate knowledge of customers and their environments
Use tools such as DOORS, POLARION or equivalent and excels in the management of requirements and decomposition of system level requirements to modules
Carry out risk management process in accordance with the EN ISO 14971 throughout product life cycle to ensure compliance and product safety
Identify development issues and facilitates in the resolution using optimal technology solutions
Supports in the Usability Engineering activities to ensure the application of human factor in the development of products or solutions to demonstrate compliance to IEC 62366 and FDA guidance
Knowledge in the application of principles of Reliability and Robustness in the development of products or solutions
Completes detailed, high quality technical documentation to capture and communicate designs
Support integration issues during development tests and ensure module / system development is successful

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

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Dfx engineering intern

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