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Medical Device Validation Jobs in Texas (NOW HIRING)

Crown Medical, Inc.

Medical Device Rep

Austin, TX · On-site

$82K - $113K/yr

Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment ... Have a valid driver's license * At least some success with abilities in business-to-business sales;

Stark Pharma Solutions Inc

CQV Engineer

Austin, TX · On-site

... Validation (CQV) activities for pharmaceutical and medical device manufacturing facilities. This role will focus on equipment qualification, utility validation, process validation, and ensuring ...

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All JobsMedical Device Validation JobsMedical Device Validation Jobs in Texas

Medical Device Validation information

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$21

$48

$72

How much do medical device validation jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for medical device validation in Texas is $48.44, according to ZipRecruiter salary data. Most workers in this role earn between $36.73 and $58.89 per hour, depending on experience, location, and employer.

What is medical device validation?

Medical device validation is the process of ensuring that a medical device consistently produces results that meet predetermined requirements and quality standards for its intended use. This involves rigorous testing and documentation to confirm that the device functions safely and effectively under real-world conditions. Validation is a critical step in regulatory approval and helps protect patient safety by verifying the device's performance and reliability. The process typically includes design validation, process validation, and software validation, depending on the type of device.

What are common challenges faced in a medical device validation role and how are they typically addressed?

Professionals in Medical Device Validation often encounter challenges such as ensuring compliance with evolving regulatory standards, managing tight project timelines, and coordinating with cross-functional teams. Addressing these challenges typically involves staying current with industry regulations (like FDA or ISO standards), meticulous documentation practices, and frequent communication with engineering, quality assurance, and manufacturing teams. Proactive problem-solving, flexibility, and a detail-oriented mindset are essential for overcoming barriers and ensuring that devices meet safety and efficacy requirements before market release.

What is the difference between Medical Device Validation vs Quality Assurance Specialist?

AspectMedical Device ValidationQuality Assurance Specialist
CertificationsISO 13485, FDA regulations, Validation protocolsISO 9001, GMP, FDA regulations
Work EnvironmentManufacturing, R&D, Regulatory complianceManufacturing, Quality control, Auditing
Primary FocusEnsuring devices meet specifications through testing and validationMaintaining quality systems and compliance

Medical Device Validation focuses on verifying that devices meet design and performance specifications through testing and validation processes. Quality Assurance Specialists oversee overall quality systems, ensuring compliance with standards and regulations. While both roles aim to ensure product safety and efficacy, Validation is more technical and testing-oriented, whereas QA is broader, covering system-wide quality management.

What are the key skills and qualifications needed to thrive as a medical device validation specialist, and why are they important?

To thrive as a Medical Device Validation Specialist, you need a solid background in engineering or life sciences, knowledge of regulatory standards (such as FDA and ISO 13485), and experience in validation protocols. Familiarity with validation tools, statistical analysis software, and documentation systems is typically required, along with certifications like Six Sigma or CQE being advantageous. Strong attention to detail, analytical thinking, and effective communication are crucial soft skills for success in this role. These skills ensure that medical devices meet safety and quality standards, supporting compliance and protecting patient health.
What are popular job titles related to Medical Device Validation jobs in Texas? For Medical Device Validation jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Medical Device Validation jobs in Texas look for? The top searched job categories for Medical Device Validation jobs in Texas are:
Medical Device Validation jobs near you
Infographic showing various Medical Device Validation job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $100,761 per year, or $48.4 per hour.

Medical Device Verification & Validation Engineer

Stark Pharma Solutions Inc

San Antonio, TX • On-site

Contractor

Posted 21 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