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Medical Device Qa Jobs in Virginia (NOW HIRING)

You will oversee the Quality Inspection Lead, Quality Inspector II, and Quality Assurance Receiving Inspector roles, as well as direct all quality inspections within the medical device and aerospace ...

Quality Assurance Specialist

Leesburg, VA ยท On-site

$75K - $90K/yr

Quality Assurance Specialist Location: Leesburg, VA (10% Travel Required) Company: VB Spine Looking ... S. and international medical device regulations * Basic knowledge of Quality Systems (CAPA, audits ...

The Quality Assurance Operations Shop Floor Specialist is part of the Quality Assurance Operations ... Minimum of 4+ years of experience within a pharmaceutical, biotech, cell therapy, or medical device ...

The Quality Assurance Operations Shop Floor Associate is part of the Quality Assurance Operations ... Minimum of 2+ years of experience within a pharmaceutical, biotech, cell therapy, or medical device ...

Quality Assurance Specialist

Blackstone, VA ยท On-site

$57K - $75K/yr

The QC/QA Lead - Mechanical manages all quality assurance and quality control activities related to ... Our full range of benefits include medical, dental, vision, disability protection, life insurance ...

Quality Assurance Specialist

Blackstone, VA ยท On-site

$57K - $75K/yr

The QC/QA Lead - Mechanical manages all quality assurance and quality control activities related to ... Our full range of benefits include medical, dental, vision, disability protection, life insurance ...

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Medical Device Qa information

See Virginia salary details

$12

$35

$68

How much do medical device qa jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for medical device qa in Virginia is $35.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.77 and $48.63 per hour, depending on experience, location, and employer.

What is a medical device QA?

Medical Device Quality Assurance (QA) professionals are responsible for ensuring that medical devices meet regulatory standards and are safe and effective for use. They develop and implement quality management systems, conduct audits, and oversee documentation throughout the product lifecycle. QA professionals also work closely with engineering, manufacturing, and regulatory teams to identify and resolve quality issues, manage risk, and ensure compliance with industry standards such as ISO 13485 and FDA regulations.

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

To thrive as a Medical Device QA, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 13485 and FDA 21 CFR Part 820), and a relevant degree in engineering or life sciences. Familiarity with quality management systems (QMS), document control software, and auditing tools is typically required, along with certifications like Certified Quality Auditor (CQA) or Six Sigma. Strong attention to detail, problem-solving abilities, and effective communication help ensure compliance and drive continuous improvement. These skills and qualities are crucial to maintaining product safety, regulatory compliance, and overall quality within the highly regulated medical device industry.

What are some common challenges faced by medical device QA professionals, and how can they be addressed?

Medical Device QA professionals often encounter challenges such as navigating complex regulatory requirements, ensuring product consistency, and keeping up with frequent changes in standards. Addressing these challenges typically involves staying current with FDA and ISO updates, maintaining robust documentation practices, and fostering clear communication with cross-functional teams like R&D and manufacturing. Regular training sessions and proactive risk management strategies also help QA professionals ensure quality and compliance throughout the product lifecycle.

What is the difference between Medical Device Qa vs Medical Device Quality Inspector?

AspectMedical Device QaMedical Device Quality Inspector
CertificationsISO 13485, FDA regulations, Six SigmaISO 13485, FDA regulations, Six Sigma
Work EnvironmentDesign, development, and process oversight in manufacturingInspection and testing on production lines
ResponsibilitiesEnsuring quality systems and complianceInspecting products for defects and conformance

Medical Device Qa professionals focus on quality assurance processes, compliance, and system improvements, while Medical Device Quality Inspectors primarily perform product inspections and defect detection. Both roles require similar certifications and work within the medical device industry, but their daily tasks and focus areas differ significantly.

What are popular job titles related to Medical Device Qa jobs in Virginia?

For Medical Device Qa jobs in Virginia, the most frequently searched job titles are:

Infographic showing various Medical Device Qa job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $74,419 per year, or $35.8 per hour.

Senior Quality Assurance Engineer, Medical Devices

Pop-Up Talent

Charlottesville, VA โ€ข On-site

$75K - $105K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

New


Job description

Senior Quality Assurance Engineer – Medical Devices
Charlottesville, VA 22911

  • Department: Quality Assurance / Regulatory Affairs
  • Reports To: Director, Quality and Design Assurance Engineering

 
100% onsite, Relocation assistance provided
 
POSITION SUMMARY:

  • MicroAire is seeking talented Quality Engineers at multiple experience levels. Candidates may be considered for either a Quality Assurance Engineer or Senior Quality Assurance Engineer position based on qualifications, experience, and demonstrated capabilities
  • The Quality Assurance Engineer supports and leads quality engineering activities associated with new product development, sustaining engineering, supplier quality, and Quality Management System (QMS) initiatives within a regulated medical device environment. This role partners with cross-functional teams to ensure products, processes, and systems meet quality, regulatory, and customer requirements while supporting innovation, operational excellence, and continuous improvement. Depending on experience and qualifications, the successful candidate may be hired at the Quality Assurance Engineer or Senior Quality Assurance Engineer level

 
ESSENTIAL DUTIES AND RESPONSIBILITIES:

  • Support and/or lead quality engineering activities related to new product development, design control, and sustaining engineering programs
  • Participate in design verification, design validation, risk management, process validation, packaging validation, sterilization validation, and design transfer activities
  • Develop, execute, and review validation and qualification protocols and reports, including IQ/OQ/PQ activities
  • Ensure compliance with applicable FDA regulations, ISO standards, company procedures, and other regulatory requirements
  • Support and/or lead CAPA, complaint investigations, nonconformance investigations, root cause analysis, and corrective action activities
  • Evaluate product and process changes and assess impact on product quality, validation status, and regulatory compliance
  • Collaborate with R&D, Manufacturing, Regulatory Affairs, Supply Chain, and Operations teams to drive quality objectives and support product launches
  • Support supplier quality activities including supplier qualification, audits, incoming quality issues, and material discrepancy resolution
  • Utilize statistical analysis and data-driven decision-making to evaluate process capability, quality trends, and product performance
  • Participate in quality metrics reviews and continuous improvement initiatives to improve QMS effectiveness and operational performance
  • Support internal and external audits and assist in maintaining an inspection-ready quality system
  • Assist with or lead implementation of quality system improvements, software tools, and process optimization projects
  • Provide technical quality guidance to cross-functional teams and, at the senior level, mentor less experienced team members
  • Perform other duties as assigned

 
EDUCATION AND EXPERIENCE:
Required

  • Bachelor's degree in Engineering, Science, or a related technical discipline

 
For Quality Assurance Engineer

  • At least 0 to 3 years of quality, manufacturing, or engineering experience
  • Experience in a regulated manufacturing environment preferred
  • Knowledge of FDA, ISO 13485, CAPA, validation, and quality systems preferred

 
For Senior Quality Assurance Engineer

  • At least 6+ years of quality or manufacturing engineering experience
  • Experience in medical devices or another highly regulated industry required
  • Demonstrated experience leading CAPAs, risk management activities, validation programs, supplier quality initiatives, and quality improvement projects
  • Prior experience mentoring or providing technical leadership preferred

 
PREFERRED QUALIFICATIONS

  • Medical device industry experience
  • Supplier quality experience
  • ASQ Certified Quality Engineer (CQE) or other ASQ certification
  • Lean Six Sigma certification or experience
  • Experience with statistical analysis, process capability studies, and quality improvement methodologies

 
We are an equal opportunity employer, and we are an organization that values diversity. We welcome applications from all qualified candidates, including minorities and persons with disabilities.
 
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