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Sr. Test Engineer

Medtronic

Sr. Test Engineer

full-timePosted: Jan 15, 2026

Job Description

We anticipate the application window for this opening will close on - 12 Mar 2026


 

Position Description:         

Sr. Test Engineer for Medtronic, Inc., located in Boxborough, MA. Responsible for providing software R&D and software test engineering support to ensure the successful development of Medtronic Neurovascular devices, design transfers, scale-up and ongoing operational support. Evaluate requirements for quality and completeness to ensure they meet the user’s needs. Test advanced image reconstruction and processing algorithms. Generate test protocols based on product requirements and project needs. Ensure software applications and systems software meet technical and functional requirements. Perform workflow analysis, document test results and recommend quality improvements. Responsible for medical device product verification, developing test protocols, planning, and tracking project team progress. Coordinate New Product Design (NPD) including reviewing requirements, design, usability, risk assessment and defects. Leverage various Software Development Life Cycle (SDLC) methodologies for software and hardware verification, troubleshooting, and identification and cataloging of software defects. Navigate the complexities of various medical device regulations and requirements to include FDA 21 CFR Part 11, ISO 14971, ISO 13485 and IEC 62304. Review test automation frameworks, tools, techniques, and methodologies, and utilizing automation tools including Azure DevOps, LabVIEW, and Test-Complete. Utilize Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). Work with high voltage, small form factor X-Ray generators and sources including SEDECAL generators, cone-beam X-Ray, X-Ray detector panels for medical imaging, including Varex flat detector panels. Ensure compliance with Industry standard medical imaging tools for 2D and 3D image evaluation and analysis with ImageJ software application, including Catphan Phantom, Modulation Transfer Function (MTF) Phantom Disk Stack, ACR Computed Tomography (CT) Phantom, Corgi Cone-Beam Computed Tomography (CBCT) Phantom, Fluoroscopic Resolution Test Tool, Spatial resolution tool and Contrast-Resolution Tool, and 45-cm acrylic radiopaque rulers. Leverage X-Ray dose measurement and evaluation tools including RTI-Piranha, RTI-barracuda, RTI-Ocean software, Dose Area Product (DAP) meter and pencil probe ion chambers and 16cm Computed Tomography Dose Indicator (CTDI) Dose Phantom and 32cm CTDI Dose Phantom.  The position allows a hybrid work model and requires the employee to be onsite at the Boxborough, MA location 4 days per week.  Relocation assistance not available.  #LI-DNI.

Basic Qualifications:          

Requires a Master’s degree in Electrical, Mechanical, or Biomedical Engineering or Computer Science or related engineering or technical field and two (2) years of experience as an R&D engineer, software engineer, or test engineer. Must possess at least two (2) years of experience with each of the following: medical device product verification; test engineering for new product design; SDLC methodologies for software and hardware verification, troubleshooting, and identification and cataloging of software defects; FDA 21 CFR Part 11, ISO 14971, ISO 13485, and IEC 62304; reviewing test automation frameworks, tools, techniques, and methodologies, utilizing Azure DevOps, LabVIEW, and Test-Complete; GMP and GDP; high voltage, small form factor X-Ray generators and sources including SEDECAL generators, cone-beam X-Ray, X-Ray detector panels for medical imaging, including Varex flat detector panels; ImageJ software application; Catphan Phantom, MTF Phantom Disk Stack, ACR CT Phantom, Corgi CBCT Phantom, Fluoroscopic Resolution Test Tool, Spatial resolution tool and Contrast-Resolution Tool, and 45-cm acrylic radiopaque rulers; and RTI-Piranha, RTI-barracuda, RTI-Ocean software, DAP meter and pencil probe ion chambers, 16cm CTDI Dose Phantom, and 32cm CTDI Dose Phantom. The position allows a hybrid work model and requires the employee to be onsite at the Boxborough, MA location 4 days per week.

Salary: $107,000 to $154,800 per year

The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).

The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).

Regular employees are those who are not temporary, such as interns.  Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.

Further details are available at the link below:

Medtronic benefits and compensation plans

Locations

  • Boxborough, Massachusetts, United States of America

Salary

107,000 - 154,800 USD / yearly

Skills Required

  • software R&D and software test engineeringintermediate
  • test advanced image reconstruction and processing algorithmsintermediate
  • test protocols generationintermediate
  • workflow analysisintermediate
  • medical device product verificationintermediate
  • project planning and trackingintermediate
  • New Product Design (NPD) coordinationintermediate
  • requirements reviewintermediate
  • design reviewintermediate
  • usability reviewintermediate
  • risk assessmentintermediate
  • defects managementintermediate
  • Software Development Life Cycle (SDLC) methodologiesintermediate
  • software and hardware verificationintermediate
  • troubleshootingintermediate
  • software defects identification and catalogingintermediate
  • medical device regulations (FDA 21 CFR Part 11, ISO 14971, ISO 13485, IEC 62304)intermediate
  • test automation frameworks reviewintermediate
  • automation tools (Azure DevOps, LabVIEW, Test-Complete)intermediate
  • Good Manufacturing Practices (GMP)intermediate
  • Good Documentation Practices (GDP)intermediate
  • high voltage small form factor X-Ray generators (SEDECAL)intermediate
  • cone-beam X-Rayintermediate
  • X-Ray detector panels (Varex flat detector panels)intermediate
  • medical imaging tools (ImageJ, Catphan Phantom, MTF Phantom Disk Stack, ACR CT Phantom, Corgi CBCT Phantom, Fluoroscopic Resolution Test Tool, Spatial resolution tool, Contrast-Resolution Tool, 45-cm acrylic radiopaque rulers)intermediate
  • X-Ray dose measurement tools (RTI-Piranha, RTI-barracuda, RTI-Ocean, DAP meter, pencil probe ion chambers, 16cm CTDI Dose Phantom, 32cm CTDI Dose Phantom)intermediate

Required Qualifications

  • Master’s degree in Electrical, Mechanical, or Biomedical Engineering or Computer Science or related engineering or technical field (experience)
  • 2 years experience as R&D engineer, software engineer, or test engineer (experience)
  • 2 years medical device product verification (experience)
  • 2 years test engineering for new product design (experience)
  • 2 years SDLC methodologies for software/hardware verification, troubleshooting, defects (experience)
  • 2 years FDA 21 CFR Part 11, ISO 14971, ISO 13485, IEC 62304 (experience)
  • 2 years test automation (Azure DevOps, LabVIEW, Test-Complete) (experience)
  • 2 years GMP and GDP (experience)
  • 2 years high voltage X-Ray generators (SEDECAL), cone-beam X-Ray, Varex panels (experience)
  • 2 years ImageJ and phantoms (Catphan, MTF, ACR CT, Corgi CBCT, etc.) (experience)
  • 2 years dose tools (RTI-Piranha, etc.) (experience)

Responsibilities

  • provide software R&D and software test engineering support
  • ensure successful development of Neurovascular devices, design transfers, scale-up, operational support
  • evaluate requirements for quality and completeness
  • test advanced image reconstruction and processing algorithms
  • generate test protocols
  • ensure software meets technical and functional requirements
  • perform workflow analysis
  • document test results
  • recommend quality improvements
  • medical device product verification
  • develop test protocols
  • plan and track project team progress
  • coordinate NPD (review requirements, design, usability, risk, defects)
  • leverage SDLC for verification, troubleshooting, defects
  • navigate medical device regulations
  • review test automation frameworks and utilize tools
  • utilize GMP and GDP
  • work with X-Ray generators, sources, detectors
  • ensure compliance with medical imaging tools
  • leverage X-Ray dose measurement tools

Benefits

  • general: Health insurance
  • general: Dental insurance
  • general: Vision insurance
  • general: Health Savings Account
  • general: Healthcare Flexible Spending Account
  • general: Life insurance
  • general: Long-term disability leave
  • general: Dependent daycare spending account
  • general: Tuition assistance/reimbursement
  • general: Simple Steps (global well-being program)
  • general: Incentive plans
  • general: 401(k) plan plus employer contribution and match
  • general: Short-term disability
  • general: Paid time off
  • general: Paid holidays
  • general: Employee Stock Purchase Plan
  • general: Employee Assistance Program
  • general: Non-qualified Retirement Plan Supplement
  • general: Capital Accumulation Plan

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Medtronic logo

Sr. Test Engineer

Medtronic

Sr. Test Engineer

full-timePosted: Jan 15, 2026

Job Description

We anticipate the application window for this opening will close on - 12 Mar 2026


 

Position Description:         

Sr. Test Engineer for Medtronic, Inc., located in Boxborough, MA. Responsible for providing software R&D and software test engineering support to ensure the successful development of Medtronic Neurovascular devices, design transfers, scale-up and ongoing operational support. Evaluate requirements for quality and completeness to ensure they meet the user’s needs. Test advanced image reconstruction and processing algorithms. Generate test protocols based on product requirements and project needs. Ensure software applications and systems software meet technical and functional requirements. Perform workflow analysis, document test results and recommend quality improvements. Responsible for medical device product verification, developing test protocols, planning, and tracking project team progress. Coordinate New Product Design (NPD) including reviewing requirements, design, usability, risk assessment and defects. Leverage various Software Development Life Cycle (SDLC) methodologies for software and hardware verification, troubleshooting, and identification and cataloging of software defects. Navigate the complexities of various medical device regulations and requirements to include FDA 21 CFR Part 11, ISO 14971, ISO 13485 and IEC 62304. Review test automation frameworks, tools, techniques, and methodologies, and utilizing automation tools including Azure DevOps, LabVIEW, and Test-Complete. Utilize Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). Work with high voltage, small form factor X-Ray generators and sources including SEDECAL generators, cone-beam X-Ray, X-Ray detector panels for medical imaging, including Varex flat detector panels. Ensure compliance with Industry standard medical imaging tools for 2D and 3D image evaluation and analysis with ImageJ software application, including Catphan Phantom, Modulation Transfer Function (MTF) Phantom Disk Stack, ACR Computed Tomography (CT) Phantom, Corgi Cone-Beam Computed Tomography (CBCT) Phantom, Fluoroscopic Resolution Test Tool, Spatial resolution tool and Contrast-Resolution Tool, and 45-cm acrylic radiopaque rulers. Leverage X-Ray dose measurement and evaluation tools including RTI-Piranha, RTI-barracuda, RTI-Ocean software, Dose Area Product (DAP) meter and pencil probe ion chambers and 16cm Computed Tomography Dose Indicator (CTDI) Dose Phantom and 32cm CTDI Dose Phantom.  The position allows a hybrid work model and requires the employee to be onsite at the Boxborough, MA location 4 days per week.  Relocation assistance not available.  #LI-DNI.

Basic Qualifications:          

Requires a Master’s degree in Electrical, Mechanical, or Biomedical Engineering or Computer Science or related engineering or technical field and two (2) years of experience as an R&D engineer, software engineer, or test engineer. Must possess at least two (2) years of experience with each of the following: medical device product verification; test engineering for new product design; SDLC methodologies for software and hardware verification, troubleshooting, and identification and cataloging of software defects; FDA 21 CFR Part 11, ISO 14971, ISO 13485, and IEC 62304; reviewing test automation frameworks, tools, techniques, and methodologies, utilizing Azure DevOps, LabVIEW, and Test-Complete; GMP and GDP; high voltage, small form factor X-Ray generators and sources including SEDECAL generators, cone-beam X-Ray, X-Ray detector panels for medical imaging, including Varex flat detector panels; ImageJ software application; Catphan Phantom, MTF Phantom Disk Stack, ACR CT Phantom, Corgi CBCT Phantom, Fluoroscopic Resolution Test Tool, Spatial resolution tool and Contrast-Resolution Tool, and 45-cm acrylic radiopaque rulers; and RTI-Piranha, RTI-barracuda, RTI-Ocean software, DAP meter and pencil probe ion chambers, 16cm CTDI Dose Phantom, and 32cm CTDI Dose Phantom. The position allows a hybrid work model and requires the employee to be onsite at the Boxborough, MA location 4 days per week.

Salary: $107,000 to $154,800 per year

The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).

The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).

Regular employees are those who are not temporary, such as interns.  Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.

Further details are available at the link below:

Medtronic benefits and compensation plans

Locations

  • Boxborough, Massachusetts, United States of America

Salary

107,000 - 154,800 USD / yearly

Skills Required

  • software R&D and software test engineeringintermediate
  • test advanced image reconstruction and processing algorithmsintermediate
  • test protocols generationintermediate
  • workflow analysisintermediate
  • medical device product verificationintermediate
  • project planning and trackingintermediate
  • New Product Design (NPD) coordinationintermediate
  • requirements reviewintermediate
  • design reviewintermediate
  • usability reviewintermediate
  • risk assessmentintermediate
  • defects managementintermediate
  • Software Development Life Cycle (SDLC) methodologiesintermediate
  • software and hardware verificationintermediate
  • troubleshootingintermediate
  • software defects identification and catalogingintermediate
  • medical device regulations (FDA 21 CFR Part 11, ISO 14971, ISO 13485, IEC 62304)intermediate
  • test automation frameworks reviewintermediate
  • automation tools (Azure DevOps, LabVIEW, Test-Complete)intermediate
  • Good Manufacturing Practices (GMP)intermediate
  • Good Documentation Practices (GDP)intermediate
  • high voltage small form factor X-Ray generators (SEDECAL)intermediate
  • cone-beam X-Rayintermediate
  • X-Ray detector panels (Varex flat detector panels)intermediate
  • medical imaging tools (ImageJ, Catphan Phantom, MTF Phantom Disk Stack, ACR CT Phantom, Corgi CBCT Phantom, Fluoroscopic Resolution Test Tool, Spatial resolution tool, Contrast-Resolution Tool, 45-cm acrylic radiopaque rulers)intermediate
  • X-Ray dose measurement tools (RTI-Piranha, RTI-barracuda, RTI-Ocean, DAP meter, pencil probe ion chambers, 16cm CTDI Dose Phantom, 32cm CTDI Dose Phantom)intermediate

Required Qualifications

  • Master’s degree in Electrical, Mechanical, or Biomedical Engineering or Computer Science or related engineering or technical field (experience)
  • 2 years experience as R&D engineer, software engineer, or test engineer (experience)
  • 2 years medical device product verification (experience)
  • 2 years test engineering for new product design (experience)
  • 2 years SDLC methodologies for software/hardware verification, troubleshooting, defects (experience)
  • 2 years FDA 21 CFR Part 11, ISO 14971, ISO 13485, IEC 62304 (experience)
  • 2 years test automation (Azure DevOps, LabVIEW, Test-Complete) (experience)
  • 2 years GMP and GDP (experience)
  • 2 years high voltage X-Ray generators (SEDECAL), cone-beam X-Ray, Varex panels (experience)
  • 2 years ImageJ and phantoms (Catphan, MTF, ACR CT, Corgi CBCT, etc.) (experience)
  • 2 years dose tools (RTI-Piranha, etc.) (experience)

Responsibilities

  • provide software R&D and software test engineering support
  • ensure successful development of Neurovascular devices, design transfers, scale-up, operational support
  • evaluate requirements for quality and completeness
  • test advanced image reconstruction and processing algorithms
  • generate test protocols
  • ensure software meets technical and functional requirements
  • perform workflow analysis
  • document test results
  • recommend quality improvements
  • medical device product verification
  • develop test protocols
  • plan and track project team progress
  • coordinate NPD (review requirements, design, usability, risk, defects)
  • leverage SDLC for verification, troubleshooting, defects
  • navigate medical device regulations
  • review test automation frameworks and utilize tools
  • utilize GMP and GDP
  • work with X-Ray generators, sources, detectors
  • ensure compliance with medical imaging tools
  • leverage X-Ray dose measurement tools

Benefits

  • general: Health insurance
  • general: Dental insurance
  • general: Vision insurance
  • general: Health Savings Account
  • general: Healthcare Flexible Spending Account
  • general: Life insurance
  • general: Long-term disability leave
  • general: Dependent daycare spending account
  • general: Tuition assistance/reimbursement
  • general: Simple Steps (global well-being program)
  • general: Incentive plans
  • general: 401(k) plan plus employer contribution and match
  • general: Short-term disability
  • general: Paid time off
  • general: Paid holidays
  • general: Employee Stock Purchase Plan
  • general: Employee Assistance Program
  • general: Non-qualified Retirement Plan Supplement
  • general: Capital Accumulation Plan

Target Your Resume for "Sr. Test Engineer" , Medtronic

Get personalized recommendations to optimize your resume specifically for Sr. Test Engineer. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Sr. Test Engineer" , Medtronic

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score
Quiz Challenge

Answer 10 quick questions to check your fit for Sr. Test Engineer @ Medtronic.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.