Medical Device Verification & Validation Engineer Location: San Antonio, TX (100% Onsite) Duration ... Manage multiple projects while supporting timely product development milestones. Required ...
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Medical Device Verification & Validation Engineer Location: San Antonio, TX (100% Onsite) Duration ... Manage multiple projects while supporting timely product development milestones. Required ...
Firmware Test Engineer
Maple Grove, MN · On-site
... medical device verification standards and compliance Preferred: • Class II/Class III medical ... Validation • Embedded Systems Testing • Requirements Traceability • Risk-Based Testing • ...
Firmware Test Engineer
Maple Grove, MN · On-site
... medical device verification standards and compliance Preferred: • Class II/Class III medical ... Validation • Embedded Systems Testing • Requirements Traceability • Risk-Based Testing • ...
DEKA Research & Development, located in Manchester, NH, is seeking a Verification & Validation Test Engineer to work in a dynamic medical device R&D environment. This is a high visibility role with a ...
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DEKA Research & Development, located in Manchester, NH, is seeking a Verification & Validation Test Engineer to work in a dynamic medical device R&D environment. This is a high visibility role with a ...
Support software planning, requirements management, verification, validation, traceability, risk ... Strong working knowledge of medical device software lifecycle processes, design controls ...
Support software planning, requirements management, verification, validation, traceability, risk ... Strong working knowledge of medical device software lifecycle processes, design controls ...
... Management Plans. * Perform oversight on the Contractor's compliance to the CP1 VV&SC Contract requirements and the Verification Validation & Self-Certification Plan requirements. * Review the ...
... Management Plans. * Perform oversight on the Contractor's compliance to the CP1 VV&SC Contract requirements and the Verification Validation & Self-Certification Plan requirements. * Review the ...
DEKA Research and Development, located in Manchester, NH, has an immediate opening for a Junior Verification & Validation Test Engineer to work in a dynamic medical device R&D environment. Test ...
DEKA Research and Development, located in Manchester, NH, has an immediate opening for a Junior Verification & Validation Test Engineer to work in a dynamic medical device R&D environment. Test ...
DEKA Research and Development, located in Manchester, NH, has an immediate opening for a Junior Verification & Validation Test Engineer to work in a dynamic medical device R&D environment. Test ...
DEKA Research and Development, located in Manchester, NH, has an immediate opening for a Junior Verification & Validation Test Engineer to work in a dynamic medical device R&D environment. Test ...
Senior Medical Device Engineer
Blue Ash, OH · On-site
$96K - $131K/yr
... Management, Verification & Validation (V&V), Supplier Quality, and Process Validation . Key ... Medical Device Project Engineer.
Senior Medical Device Engineer
Blue Ash, OH · On-site
$96K - $131K/yr
... Management, Verification & Validation (V&V), Supplier Quality, and Process Validation . Key ... Medical Device Project Engineer.
... Management Plans. * Perform oversight on the Contractor's compliance to the CP1 VV&SC Contract requirements and the Verification Validation & Self-Certification Plan requirements. * Review the ...
... Management Plans. * Perform oversight on the Contractor's compliance to the CP1 VV&SC Contract requirements and the Verification Validation & Self-Certification Plan requirements. * Review the ...
You'll be designing and executing verification and validation strategies for complex robotic ... for medical device software * Proficiency in requirements management and traceability tools (e.g ...
You'll be designing and executing verification and validation strategies for complex robotic ... for medical device software * Proficiency in requirements management and traceability tools (e.g ...
This is a role tailor-made for someone who has dedicated their career to excellence in quality management, particularly in the medical device industry. You've spent years honing your craft, mastering ...
This is a role tailor-made for someone who has dedicated their career to excellence in quality management, particularly in the medical device industry. You've spent years honing your craft, mastering ...
Client Manager - Medical Device QMS Auditor
Concord, NC · On-site
$98K - $123K/yr
Medical Device QMS Auditor Location: Colorado BSI (British Standards Institution) is the global ... verification/validation, and testing activities, ensuring compliance with ISO 13485, CE Marking ...
Client Manager - Medical Device QMS Auditor
Concord, NC · On-site
$98K - $123K/yr
Medical Device QMS Auditor Location: Colorado BSI (British Standards Institution) is the global ... verification/validation, and testing activities, ensuring compliance with ISO 13485, CE Marking ...
Client Manager - Medical Device QMS Auditor
$98K - $123K/yr
Medical Device QMS Auditor Location: Colorado BSI (British Standards Institution) is the global ... verification/validation, and testing activities, ensuring compliance with ISO 13485, CE Marking ...
Client Manager - Medical Device QMS Auditor
$98K - $123K/yr
Medical Device QMS Auditor Location: Colorado BSI (British Standards Institution) is the global ... verification/validation, and testing activities, ensuring compliance with ISO 13485, CE Marking ...
... medical device manufacture of safe and effective devices. To assist and train employees where ... Monitors, maintains and assists with validation, sterilization, risk management and design ...
... medical device manufacture of safe and effective devices. To assist and train employees where ... Monitors, maintains and assists with validation, sterilization, risk management and design ...
Program Manager - Medical Device
Beverly, MA · On-site
$120K - $140K/yr
Drive all phases of the product development cycle, including feasibility, concept, validation ... Medical Device or related industry. * 6+years' experience in Project/Program Management in a ...
Program Manager - Medical Device
Beverly, MA · On-site
$120K - $140K/yr
Drive all phases of the product development cycle, including feasibility, concept, validation ... Medical Device or related industry. * 6+years' experience in Project/Program Management in a ...
Do you have the career opportunities as a Contracts Manager, Medical Device Management that you want with your current employer? We have an exciting opportunity for you to join HealthTrust which is ...
Do you have the career opportunities as a Contracts Manager, Medical Device Management that you want with your current employer? We have an exciting opportunity for you to join HealthTrust which is ...
Program Manager - Medical Device
Beverly, MA · On-site
$120K - $140K/yr
Drive all phases of the product development cycle, including feasibility, concept, validation ... Medical Device or related industry. * 6+ years' experience in Project/Program Management in a ...
Program Manager - Medical Device
Beverly, MA · On-site
$120K - $140K/yr
Drive all phases of the product development cycle, including feasibility, concept, validation ... Medical Device or related industry. * 6+ years' experience in Project/Program Management in a ...
Medical Device Test Engineer
Waukesha, WI · On-site
As a Medical Device Test Engineer, you will be part of the Quality Assurance department supporting ... Conduct verification & validation (V&V) activities for product releases * Log, track, and validate ...
Medical Device Test Engineer
Waukesha, WI · On-site
As a Medical Device Test Engineer, you will be part of the Quality Assurance department supporting ... Conduct verification & validation (V&V) activities for product releases * Log, track, and validate ...
This is a role tailor-made for someone who has dedicated their career to excellence in quality management, particularly in the medical device industry. You've spent years honing your craft, mastering ...
This is a role tailor-made for someone who has dedicated their career to excellence in quality management, particularly in the medical device industry. You've spent years honing your craft, mastering ...
Validation Manager
Hercules, CA · On-site
Serve as Subject Matter Expert (SME) for all verification and validation activities Develop and ... of experience in medical device validation/FDA regulated industry. 3-5 years of management ...
Validation Manager
Hercules, CA · On-site
Serve as Subject Matter Expert (SME) for all verification and validation activities Develop and ... of experience in medical device validation/FDA regulated industry. 3-5 years of management ...
Manager Medical Device Verification Validation information
See salary details
$47.5K - $57.8K
1% of jobs
$57.8K - $68K
4% of jobs
$76.6K is the 25th percentile. Wages below this are outliers.
$68K - $78.3K
24% of jobs
$78.3K - $88.6K
9% of jobs
The median wage is $96K / yr.
$88.6K - $98.9K
17% of jobs
$98.9K - $109.1K
8% of jobs
$109.1K - $119.4K
5% of jobs
$126.3K is the 75th percentile. Wages above this are outliers.
$119.4K - $129.7K
11% of jobs
$129.7K - $140K
8% of jobs
$140K - $150.2K
6% of jobs
$150.2K - $160.5K
8% of jobs
$47.5K
$105.4K
$160.5K
How much do manager medical device verification validation jobs pay per year?
As of Sep 10, 2026, the average yearly pay for manager medical device verification validation in the United States is $105,415.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $132,000.00 per year, depending on experience, location, and employer.
What are popular job titles related to Manager Medical Device Verification Validation jobs?
For Manager Medical Device Verification Validation jobs, the most frequently searched job titles are:
Medical Device Verification & Validation Engineer
San Antonio, TX • On-site
Stark Pharma Solutions Inc
Contractor
Re-posted 20 days ago
Job description
Hi,
My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Medical Device V&V Engineer position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows
Position: Medical Device Verification & Validation Engineer
Location: San Antonio, TX (100% Onsite)
Duration: 12+ Month Contract
Job Overview
We are seeking a Medical Device Verification & Validation Engineer to support new product development and sustaining engineering initiatives. The ideal candidate will have strong experience in mechanical verification and validation, protocol development, statistical analysis, and testing of sterile medical devices within a regulated environment.
Key Responsibilities
- Support cross-functional teams throughout new product development and sustaining engineering activities.
- Develop, execute, and document Design Verification & Validation (V&V) protocols and reports.
- Perform functional, performance, packaging, and reliability testing for medical devices.
- Analyze test data using Minitab and other statistical tools to support product verification.
- Conduct product stability and shelf-life testing for sterile medical devices.
- Own V&V documentation within the Design History File (DHF).
- Ensure compliance with design controls, FDA regulations, and applicable industry standards.
- Collaborate with global engineering, quality, and operations teams to standardize verification methods and testing procedures.
- Manage multiple projects while supporting timely product development milestones.
Required Qualifications
- Bachelor's degree in Mechanical Engineering or related discipline.
- 4+ years of Verification & Validation experience within the Medical Device industry.
- Hands-on experience with Design Verification & Validation activities, including protocol development, execution, and reporting.
- Strong experience using Minitab or other statistical analysis software.
- Knowledge of product stability testing and shelf-life validation for sterile medical devices.
- Experience working on new product development (NPD) and cross-functional engineering teams.
I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.
Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/
Thank you,
Karthik Mutyala
Recruiting Manager
Stark Pharma Solutions Inc
Email: karthik@starkpharma.com
15 Corporate Place S, Suite 350,
Piscataway, New Jersey 08854
www.starkpharma.com