Device Validation Engineer Job at Microsoft Corporation (Hyderabad)

Systems Validation Engineer

Cricut is seeking a versatile Systems Validation Engineer (we also call this a F...

Location

United States , South Jordan

Salary:

Not provided

Cricut

Expiration Date

Until further notice

Requirements

Experience working in a technical development team
Experience in writing clear, concise and comprehensive test scenarios, test cases and test plans
Experience in executing test cases, debugging & analyzing results, reporting & tracking defects, and providing updates to stakeholders
Good knowledge of USB, Bluetooth classic, BLE, and Wi-Fi communication protocols
Good experience in microcontrollers, DC motors (Steppers and Servos), and motor drivers
Some experience with sensing, sampling, and feedback control systems
Some experience in testing USB/wireless device software/apps on Windows and Mac
Intermediate or higher programming experience in Swift, Dart, C/C++ and Python
Good written and verbal communication skills
Able to communicate project plans with contract manufacturers in Asia

Job Responsibility

Testing and qualifying Firmware and Hardware for product releases
Testing Firmware's for the new and existing hardware products and communicating with development teams
Represent QA concerns in cross-functional team meetings and provide valuable end-user feedback to improve the customer experience
Develop and execute an organized test plan to release high quality products to the market on schedule

Fulltime

Director Systems Engineering

As the Director Systems Engineering, Infusion Systems, you will lead the develop...

Location

United States , Round Lake

Salary:

184000.00 - 253000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's or Master’s degree in Systems Engineering, Biomedical Engineering or a related field
Minimum of 10 years of experience in systems engineering, with a focus on medical fluid management devices (electromechanical pumps) in the medical device industry
Demonstrated experience leading, developing and managing engineering teams in a highly regulated environment
Strong technical skills, with a deep understanding of systems engineering principles and practices
Excellent communication and collaboration skills, with the ability to work effectively with cross-functional teams
Critical thinker, strong problem-solver, analytical
Proactive approach to project management, able to address potential risks and issues before they become critical
Organized, able to prioritize tasks effectively
Passionate about ensuring the safety and effectiveness of medical devices, and committed to delivering high-quality products that meet user needs
Customer focus, with a deep understanding of user needs and preferences, and a commitment to designing and developing products that meet these needs

Job Responsibility

Lead and develop global systems engineering teams based in Round Lake, IL, Bangalore, India, and Medina, NY
Create, effectively communicate, and deploy the strategy for the team that aligns with the overall systems organization strategic plan
Own capturing system use environments, workflows, user needs and use cases across all infusion systems platforms
Lead systems design validation across all platforms
Drive creation and verification of comprehensive system requirements for new and existing infusion systems pumps, administration sets, elastomerics, and accessories, ensuring they are complete, accurate, and aligned with user needs and business objectives
Collaborate to ensure alignment and traceability of requirements throughout the product development process
Implement and maintain a robust systems risk management framework to identify, analyze, and mitigate potential risks
Lead resource demand planning, allocation, and actuals
Recruit, mentor, and lead a multi-disciplinary engineering team, fostering a culture of innovation, collaboration, and continuous improvement
Conduct regular risk assessments and reviews ensuring compliance with medical device regulations and standards

What we offer

Support for parents
Continuing education/professional development
Employee health & well-being benefits
Paid time off
2 days a year to volunteer
Medical and dental coverage that starts on day one
Basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP) with company matching
Flexible Spending Accounts

Fulltime

Principal Electrical Engineer

We are seeking a highly experienced and technically driven Principal Electrical ...

Location

United States , Plymouth

Salary:

Not provided

Blackrock Neurotech

Expiration Date

Until further notice

Requirements

B.S. in Electrical Engineering, Biomedical Engineering, or related field
10+ years of experience in electrical design for active implantable medical devices (AIMDs), such as neurostimulators, pacemakers, or cochlear implants
Proven track record designing low-noise analog front ends, stimulation circuits, power management, and wireless telemetry (RF and inductive coupling)
Deep knowledge of implant power and safety considerations
Familiarity with closed-loop control systems and physiological signal acquisition
Experience operating within a quality system supporting Class III systems
Proficient in analog/digital mixed-signal design tools (e.g., SPICE, Altium, Cadence)
Strong understanding of embedded systems interfaces (SPI, I²C, UART)
Experience with simulation, modeling, and reliability analysis (Monte Carlo, tolerance analysis)
Knowledge of relevant standards: ISO 14708, IEC 60601, ISO 14971, ISO 13485, FDA Class III design controls

Job Responsibility

Develop circuit-level designs for ultra-low-power analog front ends, stimulation drivers, power management, and telemetry interfaces
Define and maintain electrical requirements, design specifications, and interface documents
Lead the design of production test equipment and processes
Perform schematic capture, circuit simulation, component selection, and PCB layout guidance for implantable and external system electronics
Collaborate with firmware and algorithm teams to enable closed-loop control of stimulation based on sensed physiological signals
Drive prototype development, bench testing, and design characterization for implantable hardware
Provide technical leadership to multidisciplinary design teams and mentor junior engineers
Champion design best practices, design for reliability (DfR), and design for manufacturability (DfM)
Driving verification and validation (V&V) activities, including unit, integration, and system-level testing to ensure reliability and traceability
Lead design verification testing (DVT) and verification planning to ensure compliance with medical device standards and safety requirements

Fulltime

Senior Principal Software Quality Engineer

As a Senior Principal Software Quality Engineer at Baxter, you will play a criti...

Location

United States , Raleigh

Salary:

120000.00 - 165000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

B.S. in Engineering or other technical degree required, preferably Computer Science/Engineering or Electronics/Electrical Engineering
Software Quality experience is highly sought, especially in the medical device industry
Knowledge of AAMI 62304 standard is valuable
Minimum 8 years of experience in medical device or other regulated technical industry (e.g., aerospace, automotive, defense) in a design/development/quality role or in a role closely connected to design/development/quality is required
Proven ability to perform and influence in cross-functional team environments and utilize effective interpersonal skills
2+ years of Quality experience desired
Product Design experience may be considered in lieu of Quality Assurance experience
Software development experience in a regulated industry is desirable
Knowledge of software development lifecycle processes and standards required
Understanding of software development tools and methods for medical devices and/or other regulated industries desirable

Job Responsibility

Responsible for all Design Assurance functions as a core team member on new product development (NPD) teams, ensuring the team complies with all portions of Design Control and related Quality System elements
Prepare and manage all Design Assurance required deliverables as well as support the remainder of the team in developing a quality product that meets regulatory requirements
Responsible for ensuring product development activities related to verification and validation are fully compliant to the quality system procedures
Assist in identification and mitigation of product or process-related risks

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Health & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Manufacturing Engineer

Eitan Medical is a fast-growing international medical device company that develo...

Location

Israel , Netanya

Salary:

Not provided

Eitan Medical

Expiration Date

Until further notice

Requirements

BSc in mechanical engineering from a well-known establishment
At least 5 years’ experience in manufacturing engineering at a multidisciplinary company
Good understanding of assembling and manufacturing processes (injection molding, machining, PCB manufacturing etc.)
Experience in the medical device industry and with FDA and ISO 13485 medical device regulations
Experience with single-piece flow manufacturing processes
Great problem-solving and debugging capabilities
Full control of all Microsoft Office applications
SolidWorks
Fluent English (written and verbal)
Strong technical and analytical skills

Job Responsibility

Production process establishments and improvements
Resolve the company products technical issues and continuously support and improve the products’ quality
Lead Engineering Change Orders (ECOs) in accordance with FDA/MDR regulations, including creating production files, defining assembly processes, writing work instructions, preparing drawings
Conduct technical investigations and experiments, drive for root cause identification
Perform verification and validation activities for the production line
Plan, specify, implement, and maintain dedicated tools, jigs, and production equipment

Fulltime

Electrical Engineer Student

Eitan Medical is a fast-growing international medical device company that develo...

Location

Israel , Netanya

Salary:

Not provided

Eitan Medical

Expiration Date

Until further notice

Requirements

3rd year BSc student in electrical engineering from a well-known establishment
Experience in the medical device industry and with FDA and ISO 13485 medical device regulations - an advantage
Great problem-solving and debugging capabilities
Availability for 24 hours a week
Full control of all Microsoft Office applications
SolidWorks
Fluent English (written and verbal)
Strong technical and analytical skills
excellent interpersonal relationships
self-motivated

Job Responsibility

Resolve the company products technical issues and continuously support and improve the products’ quality
Conduct technical investigations and experiments, drive for root cause identification as a part of the NCMR process
Perform verification and validation activities for the production line

Parttime

Principal Product Development Engineer

The individual in this role is highly skilled and experienced and can lead and d...

Location

United States , Lake Forest

Salary:

130000.00 - 150000.00 USD / Year

Manufacturing For Design

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in mechanical or biomedical engineering or equivalent experience
7 – 10 years industry experience with a medical device company
Demonstration of excellent communication (written and oral) skills
Demonstration of excellent organizational skills with the ability to adapt to a rapidly changing environments
Prior experience with non-invasive medical devices (catheters)
Ability to present/teach detailed technical information, to all levels of company personnel and customers
Extended periods of sitting
Extended usage of a microscope
Moderate lifting

Job Responsibility

Lead and manage the product development process, from concept through to commercialization, ensuring that projects are delivered on time and within budget
Define product specifications and requirements in collaboration with cross-functional teams
Conduct thorough risk assessments and implement strategies to mitigate potential issues
Collaborate with regulatory affairs and quality assurance team to ensure compliance with all relevant regulations and standards
Collaborate with R&D on the creation of prototypes and conduct experiments to determine validity of designs
Perform and/or manage design verification, equipment qualification and product and process validation
Use CAD software (Solidworks) for part and assembly design and detail drawings
Work closely with manufacturing team to facilitate the transition from development to production
Manage the budget for product development, optimizing costs while maintaining high product quality and compliance
Engage in completing necessary documentations as well as maintaining comprehensive documentation of all product development activities, including design specifications, test results, and regulatory submissions

What we offer

Medical Insurance, Dental Insurance, and Vision Insurance, 100% paid for employee
401K Plan

Fulltime

Senior R&D Engineer, Catheters

We are hiring a Senior R&D Engineer to join our team and play a critical role in...

Location

United States , Lake Forest

Salary:

100000.00 - 130000.00 USD / Year

Manufacturing For Design

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in mechanical or biomedical engineering or equivalent experience
3-10 years industry experience with a medical device company
Demonstration of excellent communication (written and oral) skills
Demonstration of excellent organizational skills with the ability to adapt to a rapidly changing environment
Prior experience with non-invasive medical devices (catheters)
Ability to present/teach detailed technical information, to all levels of company personnel and customers

Job Responsibility

Provide technical leadership for the design and development of medical devices
Assist in the transfer of new products from R&D to production
Establish processes and manufacturing documentation for new catheter products
Identify processes/materials to fabricate new products
Use CAD software (Solidworks preferred) for part and assembly design and detail drawings
Perform experiments to determine validity of designs
Provide technical leadership for development projects
Define product requirements
Design and development of tooling
Perform or manage design verification, equipment qualification and product and process validations

What we offer

Medical Insurance, Dental Insurance, and Vision Insurance, 100% paid for employee
401K Plan

Fulltime

Device Validation Engineer

Microsoft Corporation

Location:
India , Hyderabad

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
February 01, 2026

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Contract Type:Not provided

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Job Description:

Job Responsibility:

Requirements:

Nice to have:

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