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Medical Device Validation Engineer Jobs in New Port Richey, FL

DOCSIS 3.0 and VoIP, SIP, MGCP applications testing using a CPE device Review product requirements ... Design, write and execute test plans to validate VoIP application functionality. Own and maintain ...

Sr. Engineer, R&D (Biomaterials)

Tampa, FL

$98K - $135K/yr

Job Summary of the Sr. Engineer, R&D The Sr. Engineer, Research & Development, is an experienced ... verification and validation methodologies within a regulated medical device environment.

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

Sr. Engineer, R&D

Tampa, FL · On-site

$98K - $135K/yr

Job Summary of the Sr. Engineer, R&D The Sr. Engineer, Research & Development, is an experienced ... verification and validation methodologies within a regulated medical device environment.

Sr. Engineer, R&D (Biomaterials)

Tampa, FL · On-site

$98K - $135K/yr

Job Summary of the Sr. Engineer, R&D The Sr. Engineer, Research & Development, is an experienced ... verification and validation methodologies within a regulated medical device environment.

Sr. Engineer, R&D (Biomaterials)

Tampa, FL · On-site

$98K - $135K/yr

Job Summary of the Sr. Engineer, R&D The Sr. Engineer, Research & Development, is an experienced ... verification and validation methodologies within a regulated medical device environment.

Manage validated backup and recovery processes, including restoration testing and disaster recovery ... Experience working within pharmaceutical, biotechnology, medical device, or other GMP-regulated ...

Manage validated backup and recovery processes, including restoration testing and disaster recovery ... Experience working within pharmaceutical, biotechnology, medical device, or other GMP-regulated ...

Manage validated backup and recovery processes, including restoration testing and disaster recovery ... Experience working within pharmaceutical, biotechnology, medical device, or other GMP-regulated ...

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Medical Device Validation Engineer information

See New Port Richey, FL salary details

$20

$46

$69

How much do medical device validation engineer jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for medical device validation engineer in New Port Richey, FL is $46.31, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $56.30 per hour, depending on experience, location, and employer.

What are some common challenges faced by medical device validation engineers during the validation process?

Medical Device Validation Engineers often encounter challenges such as ensuring compliance with evolving regulatory standards, managing tight project timelines, and coordinating cross-functional teams. Additionally, they must address unexpected technical issues that arise during testing and validation, and meticulously document results to meet quality and audit requirements. Effective communication and adaptability are crucial for successfully navigating these challenges and delivering safe, effective medical devices.

What does a medical device validation engineer do?

A Medical Device Validation Engineer is responsible for ensuring that medical devices meet regulatory and quality standards before they reach the market. They design and execute tests to validate that products perform as intended, documenting procedures and results to comply with industry regulations such as FDA and ISO guidelines. Their work involves collaborating with design, manufacturing, and quality assurance teams to identify risks and verify that devices are safe and effective for use. This role is crucial for patient safety and for a company's ability to market medical products globally.

Are medical device validation engineers in demand?

Medical device validation engineers are in high demand due to the increasing regulation and complexity of medical devices. They play a critical role in ensuring compliance with standards like ISO 13485 and FDA requirements, and their expertise in validation, testing, and quality assurance is sought after in the healthcare industry.

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

AspectMedical Device Validation EngineerQuality Assurance Engineer
CredentialsEngineering degree, certifications like CQE or validation-specific trainingEngineering or related degree, CQE or QA certifications
Work EnvironmentDesign validation, process validation, testing labsAudits, process improvements, compliance documentation
Industry UsageProduct development, validation phases in medical device manufacturingEnsuring overall product quality, compliance, and process control

The Medical Device Validation Engineer focuses on validating medical devices through testing and process validation, ensuring products meet regulatory standards. In contrast, the Quality Assurance Engineer oversees overall quality systems, audits, and compliance processes. Both roles require similar certifications and work within the medical device industry, but their core responsibilities differ in scope and focus.

What are the key skills and qualifications needed to thrive as a medical device validation engineer?

To thrive as a Medical Device Validation Engineer, you need a strong background in biomedical engineering or a related field, with expertise in validation protocols, regulatory compliance, and risk analysis. Familiarity with technical standards such as ISO 13485, FDA 21 CFR Part 820, and tools like statistical analysis software and validation management systems is essential. Attention to detail, problem-solving abilities, and effective communication are critical soft skills for collaborating with cross-functional teams and ensuring product safety. These skills are crucial to guarantee that medical devices meet regulatory requirements, function safely, and reach the market efficiently.

What cities near New Port Richey, FL are hiring for Medical Device Validation Engineer jobs?

Cities near New Port Richey, FL with the most Medical Device Validation Engineer job openings:

GW/Routers Validation Engineer

Stem Xpert

Tampa, FL

Contractor

Re-posted 16 days ago


Job description

Company Description

Founded in 2009 and headquartered in Ann Arbor, MI, TEKWISSEN provides a unique portfolio of innovative capabilities that seamlessly combines clients insights, strategy, design, software engineering and systems integration. Our tightly integrated offerings are tailored to each client's requirements and span the services spectrum from Application Development/Maintenance, testing, Technology Consulting & staffing. The company is primarily focused on information technology, engineering, healthcare, financial technology and contingent workforce solutions. It operates in seven business segments including Commercial, Professional & Technical, EMEA Commercial, and EMEA Professional & Technical. The company provides professional and technical expertise in the fields of Telecom, Education, Banking, Retail, e-commerce, Automotive, Life Science, Insurance, legal, healthcare, among others. It also offers outsourcing, consulting, recruitment, career transition, and vendor management services.
We strongly believe:
" If something cannot be measured, it cannot be managed. "
TEKWISSEN measures all of these processes and applies corrective interventions to manage the quality process at its core.
We are an Equal Employment Opportunity Employer M/F/V/D
Recognitions:
2015 -America's Fastest Growing Company by Inc.com
2015- SPARK FastTrack Award from Ann Arbor SPARK
2015 -Honoree of Diversity Focused Company by Corp! Magazine
2014- America's Fastest Growing Company by Inc.com
2014- Michigan 50 Companies to Watch
2014 - DiSciTech Award in Technology by Corp! Magazine
2014- DiSciTech TECHNOLOGY Company of the year by Corp! Magazine
2014- SPARK FastTrack Award from Ann Arbor SPARK
Specialties:
Enterprise Solutions, Web Development, Data Warehousing, Systems Integration, IT Security, Storage Technologies, Development and Delivery, Business Intelligence, Telecommunications, Consulting and Planning, Network design, Implementation &Administration

Job Description


RESPONSIBILITIES:
Responsibilities will focus on qualification of Technicolor /Cisco CDBU products with major customers. Products will include DOCSIS gateway products, wireless products, and hybrids from these areas. You will be responsible for the following:
DOCSIS 3.0 and VoIP, SIP, MGCP applications testing using a CPE device
Review product requirements, functional specifications, standards documents (RFCs and specs). Design, write and execute test plans to validate VoIP application functionality.
Own and maintain the test infrastructure including design and configuration of TCP/IP networks including routers/switches/CMTS, SIP servers, and other monitoring and testing equipment.
Own automation framework and develop automation scripts to validate protocol compliance, interoperability, voice path validation and feature behaviour.
Perform and analyze network packet captures to troubleshoot protocol and voice quality issues.
JOB REQUIREMENTS & QUALIFICATIONS
 Minimum of 8+ years working as test engineer or field engineer with DOCSIS and VoIP
Deep understanding of VoIP protocols and ability to read and troubleshoot call flows involving SIP, MGCP & RTP
Hands-on experience working with, configuring, and troubleshooting routers, switches, & CMTS.
Hands-on experience working with, configuring, and troubleshooting VoIP Call Agents, SIP Proxy and IMS Core
Hands-on experience using packet capture tools and analyze call flows and RTP
Experience designing and performing load, stress and performance testing including Bulk Call Generators
Hands-on experience and expertise is developing scripts using Perl, VBscript, Python, or similar scripting language
Hands-on experience with SIP automation tools
CCNP/CCIE certification is not required but is a plus.

Additional Information
Thanks & Regards
Narendra
narendra(dot)s(at)tekwissen.com
734-357-8978

stem xpert logo

About stem xpert

Sourced by ZipRecruiter

STEM Xpert, based in Ann Arbor, MI, US, is a leading company in the Science, Technology, Engineering, and Mathematics (STEM) education industry. Since their establishment, they have made an indelible mark by providing innovative services and products designed to enhance STEM learning. Their service portfolio includes comprehensive educational programs, customized learning modules and interactive STEM kits. Driven by a passion for nurturing young minds, the company's mission is to bring about an educational renaissance in the STEM field, making learning not just theoretical but practical and fun. One notable achievement for STEM Xpert has been its success in reaching a broad spectrum of learners, from school-age to adults, contributing significantly towards empowering the community's technological and scientific literacy.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2012