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Medical Device Qa Jobs in Virginia (NOW HIRING)

Caraballo Consulting & Associates L

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QA Manufacturing Engineer - Medical Device

Sterling, VA · On-site

$40 - $80/hr

Experience in the medical device industry within Quality Assurance, Validation, Manufacturing Quality, or a closely related function. * Strong working knowledge of process validation, equipment ...

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Caraballo Consulting & Associates L

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QA Manufacturing Engineer - Medical Device

Sterling, VA · On-site

$40 - $80/hr

Experience in the medical device industry within Quality Assurance, Validation, Manufacturing Quality, or a closely related function. * Strong working knowledge of process validation, equipment ...

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Asta CRS Inc.

Quality Assurance Manager

Virginia Beach, VA · On-site

$29 - $30/hr

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 ...

VB Spine

Quality Assurance Specialist

Leesburg, VA · 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 ...

Via Logic LLC

Quality Assurance (QA) Lead

Chantilly, VA · On-site

$92.30 - $166.85/hr

The QA Lead will be responsible for developing and implementing quality standards and procedures to ... medical condition, genetic information, pregnancy, family structure, marital status, ancestry ...

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Civica Rx

QA Ops Shop Floor Specialist (412)

Petersburg, VA · On-site

$75K - $90K/yr

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 ...

Civica Rx

QA Ops Shop Floor Associate (386)

Petersburg, VA · On-site

$65K - $75K/yr

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 ...

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Medical Device Qa information

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$12

$35

$68

How much do medical device qa jobs pay per hour?

As of Aug 19, 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:

What job categories do people searching Medical Device Qa jobs in Virginia look for?

The top searched job categories for Medical Device Qa jobs in Virginia are:

Medical Device Qa jobs near you
Infographic showing various Medical Device Qa job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 22% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $74,419 per year, or $35.8 per hour.

QA Manufacturing Engineer - Medical Device

Caraballo Consulting & Associates L

Sterling, VA • On-site

$40 - $80/hr

Contractor

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Job description

We are seeking a Quality Manufacturing Engineer extensive experience in Medical Devices to oversee Manufacturing Quality projects and line transfers for a Medical Device company.  The perfect candidate will perform the following activities:

Key Responsibilities:

    • Support quality assurance activities associated with transferring and starting up manufacturing operations at the new site.
    • Review, execute, and approve validation documentation, including protocols, test scripts, test data, and final reports.
    • Provide QA oversight for process validation activities to ensure processes are qualified, controlled, and appropriately documented.
    • Support equipment qualification efforts, including IQ, OQ, and PQ activities for manufacturing equipment and related systems.
    • Partner with Manufacturing, Engineering, Validation, and Quality teams to ensure validation deliverables are completed on time and in compliance with applicable procedures and regulations.
    • Assess validation packages for completeness, accuracy, traceability, and adherence to GMP and medical device quality system requirements.
    • Support investigation and resolution of validation-related deviations, discrepancies, and change controls.
    • Generate, review, and approve validation summary reports and supporting documentation for management and quality records.                  
    • Support QA activities associated with the QMS integration of 2 companies.
    • Modify SOPs to complete QMS integration.
    • Complete Change Control activities.
    • Complete the bulk download of documents and records from a Quality Management System.

   Required Qualifications:

  • Bachelor’s degree in Engineering, Quality, Life Sciences, or a related technical discipline, or equivalent relevant experience.
  • Experience in the medical device industry within Quality Assurance, Validation, Manufacturing Quality, or a closely related function.
  • Strong working knowledge of process validation, equipment qualification, and GMP requirements in a regulated manufacturing environment.
  • Demonstrated experience reviewing and approving validation documentation and technical reports.
  • Familiarity with manufacturing operations and the practical application of quality requirements on the production floor.
  • Ability to work independently while coordinating effectively with cross-functional stakeholders.
  • Strong technical writing, documentation review, and problem-solving skills.
  • Excellent attention to detail and ability to manage multiple priorities within a time-bound project.

Company Description

We are a specialized Global staffing firm that works for Fortune 500 companies in the Medical Device, Pharmaceutical, and Biotec industries, finding qualified personnel.