ZipRecruiter

Log In

1

Validation Engineer Biomedical Jobs in Raleigh, NC

Barry Wehmiller Group

Validation Engineer

Raleigh, NC · On-site

S. in Bioengineering, Biomedical Engineering, Chemical Engineering, or related technical degree ... As a Validation Engineer, you will build a meaningful and fulfilling career with the support of ...

Trimedx

Biomedical Technician lll

Raleigh, NC · On-site

Valid driver's license required; variable travel requirements depending on primary site that may ... Bachelor's degree in engineering technology preferred * Technical Certification (CBET) preferred

TRIMEDX Holdings

Biomedical Technician lll

Raleigh, NC · On-site

Valid driver's license required; variable travel requirements depending on primary site that may ... Bachelor's degree in engineering technology preferred * Technical Certification (CBET) preferred

NCSU

Lecturer - Biomedical Program

Raleigh, NC · On-site

... engineers and scientists to meet the challenges of biomedical discovery and applications of ... Preferred Qualifications N/A Required License(s) or Certification(s) N/A Valid NC Driver's License ...

NCSU

Lecturer - Biomedical Program

Raleigh, NC · On-site

... engineers and scientists to meet the challenges of biomedical discovery and applications of ... Preferred Qualifications N/A Required License(s) or Certification(s) N/A Valid NC Driver's License ...

next page

Showing results 1-20

All JobsValidation Engineer Biomedical JobsValidation Engineer Biomedical Jobs in Raleigh, NC

Validation Engineer Biomedical information

See Raleigh, NC salary details

$21

$50

$75

How much do validation engineer biomedical jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for validation engineer biomedical in Raleigh, NC is $50.54, according to ZipRecruiter salary data. Most workers in this role earn between $38.32 and $61.44 per hour, depending on experience, location, and employer.

What does a validation engineer do in biomedical?

A Validation Engineer in the biomedical industry ensures that equipment, processes, and systems used in the production of medical devices or pharmaceuticals meet regulatory standards and function as intended. Their work involves planning and executing validation protocols, documenting results, and troubleshooting any deviations. This role is crucial for maintaining product quality, patient safety, and compliance with regulatory agencies such as the FDA. Validation Engineers often collaborate with quality assurance, manufacturing, and research teams to establish and maintain validated systems throughout a product's lifecycle.

What are the key skills and qualifications needed to thrive as a validation engineer in biomedical?

To thrive as a Validation Engineer in Biomedical, you need a solid background in engineering or life sciences, knowledge of regulatory standards (such as FDA or ISO 13485), and experience with validation protocols. Familiarity with technical tools like statistical analysis software, calibration equipment, and documentation systems is essential, and certifications such as Six Sigma or CQE can be advantageous. Strong problem-solving, attention to detail, and effective communication skills help you excel in cross-functional teams and ensure compliance. These skills are crucial for maintaining product quality, meeting regulatory requirements, and ensuring patient safety in biomedical environments.

What are some typical challenges faced by validation engineers in the biomedical industry and how can they be addressed?

Validation Engineers in the biomedical field often face challenges such as keeping up with evolving regulatory requirements, managing complex documentation, and ensuring equipment or processes meet stringent quality standards. Navigating audits and working cross-functionally with R&D, manufacturing, and quality assurance teams can also be demanding. To address these challenges, staying current with industry regulations, developing strong organizational and communication skills, and maintaining meticulous records are essential for success and career growth in this role.

What is the difference between Validation Engineer Biomedical vs Quality Assurance Engineer Biomedical?

AspectValidation Engineer BiomedicalQuality Assurance Engineer Biomedical
CertificationsGMP, ISO, FDA validation certificationsGMP, ISO, audit and compliance certifications
Work EnvironmentDesign, develop, and execute validation protocols for medical devicesDevelop and maintain quality systems, audits, and process improvements
Industry UsagePrimarily in medical device manufacturing and regulatory validationAcross medical device, pharmaceutical, and biotech industries

Validation Engineer Biomedical focuses on ensuring medical devices meet regulatory validation requirements through testing and protocols. Quality Assurance Engineer Biomedical emphasizes maintaining quality systems, compliance, and process improvements. Both roles are essential in the biomedical industry but serve different functions related to validation versus quality assurance.

What are popular job titles related to Validation Engineer Biomedical jobs in Raleigh, NC?

For Validation Engineer Biomedical jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Validation Engineer Biomedical jobs in Raleigh, NC look for?

The top searched job categories for Validation Engineer Biomedical jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Validation Engineer Biomedical jobs?

Cities near Raleigh, NC with the most Validation Engineer Biomedical job openings:

Validation Engineer Biomedical jobs near you

Validation Engineer

Performance Validation, Inc

Raleigh, NC

$80K - $83K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 27 days ago

Key responsibilities

  • Develop verification and qualification deliverables such as Requirements Documents, Functional and Design Specifications, Test Protocols (IQ/OQ/PQ), and Summary Reports

  • Execute test protocols and identify and resolve non-conformances or deviations

  • Track and manage change control activities for multiple projects

Job description

About Us
Here at Performance Validation, Inc (PV) we have been providing Commissioning, Qualification, and Validation services to the life science industries for 37 years. We are a 100% employee owned company with teams in Indiana, Michigan, Illinois, Kansas, Washington, and North Carolina, and we support clients throughout the US and overseas. As an employer, PV is committed to providing growth opportunities to our employees through professional development, implementation of new services, and cultivation of new geographical areas.
About the job
Performance Validation is seeking a full-time Level 2 Validation Engineer/Specialist to join our team in Raleigh, NC The Level II Validation Engineer/Specialist reports directly to the Site Manager and will be assigned to one or more project teams headed by a Project Leader.
Responsibilities
  • Develop a sound understanding of how to properly implement technical, quality, and scientific principals necessary to meet industry and customer requirements
  • Work in a team environment to meet defined objectives based on established timelines
  • Develop verification/qualification deliverables including but not limited to Requirements Documents, Functional and Design Specifications, Test Protocols (IQ/OQ/PQ), and Summary Reports
  • Execute test protocols, including identification and resolution of non-conformances/deviations
  • Track and manage change control activities for multiple concurrent projects

Requirements you will need
Education:
  • BS/BA degree and 1-2 years in pharmaceutical or other regulated industry experience directly related to pharmaceutical validation
  • BS degrees in Biomedical Engineering, Chemical Engineering or Mechanical Engineering preferred

Experience:
  • Change and Deviation Management
  • Strong interpersonal skills. Must interact confidently with clients, other contractors, and employees
  • Possess excellent oral and written communication skills and high attention to detail
  • Cleaning, Sterlization, and Decontamination Validation experienced preferred
  • Device Assembly and Packing experience preferred

What we have to offer
  • Competitive base salary
  • Biannual profit share
  • Employee stock ownership program
  • 401(k) company match
  • Flexible time off policy
  • Paid Parental Leave
  • Internal and external training opportunities
  • Medical, vision, and dental coverage
  • Disability and life insurance
  • Cellphone stipend
  • Growth opportunities
  • Company-sponsored team building outings
  • A collaborative work environment
  • Work/life harmony
Please note that the salary range provided is a good faith estimate on the applicable range. The final salary offer will be determined after considering relevant factors, including a candidate's qualifications and experience, where appropriate.

This role involves frequent travel to client and partner sites, estimated at 30–50% depending on business needs and project cycles.
Qualified candidates must be legally authorized to be employed in the United States. Performance Validation, Inc. does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.

Apply