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Medical Device Quality Control 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

... Quality projects and line transfers for a Medical Device company. The perfect candidate will ... Complete Change Control activities. * Complete the bulk download of documents and records from a ...

Caraballo Consulting & Associates L

Be Seen First

QA Manufacturing Engineer - Medical Device

Sterling, VA · On-site

$40 - $80/hr

... Quality projects and line transfers for a Medical Device company. The perfect candidate will ... Complete Change Control activities. * Complete the bulk download of documents and records from a ...

Aurora Lifesciences

QC Team Lead

Manassas, VA · On-site

$90 - $120/hr

Lead and support a team of Quality Control and Receiving Inspection personnel. * Allocate daily ... Experience in medical device manufacturing is desirable. * Previous experience in a team leader ...

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VB Spine

Quality Control Inspector

Leesburg, VA · On-site

... quality database * Transact parts in the inventory control system (JD Edwards) * Initiate ... manufacturing (medical device experience is a plus) * Ability to read and interpret complex ...

VB Spine

Quality Control Inspector

Leesburg, VA · On-site

... quality database * Transact parts in the inventory control system (JD Edwards) * Initiate ... manufacturing (medical device experience is a plus) * Ability to read and interpret complex ...

VB Spine

Quality Control Inspector

Leesburg, VA · On-site

... quality database * Transact parts in the inventory control system (JD Edwards) * Initiate ... manufacturing (medical device experience is a plus) * Ability to read and interpret complex ...

Thermo Fisher Scientific

Lead QC Technician

Middletown, VA · On-site

$23.26 - $34.88/hr

REQUIREMENTS: • Minimum 4 years of experience in quality control within a regulated environment (pharmaceutical/medical device preferred) • Preferred Fields of Study: Chemistry, Biology, or ...

Thermo Fisher Scientific

Lead QC Technician

Middletown, VA · On-site

$23.26 - $34.88/hr

REQUIREMENTS: • Minimum 4 years of experience in quality control within a regulated environment (pharmaceutical/medical device preferred) • Preferred Fields of Study: Chemistry, Biology, or ...

Cell Tech Inc

Quality Control Technician

Dulles, VA · On-site

$17 - $20/hr

At Cell Tech, we specialize in K-12 device deployment and support, ensuring technology is ... As a Quality Control Technician, you will have an essential role within the company. You will ...

Cell Tech Inc

Quality Control Technician

Dulles, VA · On-site

$17 - $20/hr

At Cell Tech, we specialize in K-12 device deployment and support, ensuring technology is ... As a Quality Control Technician, you will have an essential role within the company. You will ...

Jjwws

Quality Control Manager

Portsmouth, VA · On-site

$110 - $130/hr

UFC criteria applicable to military medical facilities. * Commissioning processes for healthcare facilities. * Mechanical, electrical, plumbing, fire protection, medical gas, low-voltage, and ...

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Medical Device Quality Control information

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How much do medical device quality control jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for medical device quality control in Virginia is $21.29, according to ZipRecruiter salary data. Most workers in this role earn between $17.16 and $23.85 per hour, depending on experience, location, and employer.

What is medical device quality control?

Medical Device Quality Control refers to the processes and procedures used to ensure that medical devices meet safety, quality, and regulatory standards before they reach the market. This involves rigorous inspection, testing, and documentation throughout the manufacturing process to prevent defects and ensure consistent product performance. Quality control professionals work to identify issues, monitor compliance with industry regulations like ISO 13485 and FDA requirements, and help maintain the integrity of healthcare products. Their role is crucial in protecting patient safety and upholding the reputation of medical device manufacturers.

What are the key skills and qualifications needed to thrive as a medical device quality control professional?

To thrive in Medical Device Quality Control, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 13485 or FDA 21 CFR Part 820), and experience with inspection techniques, often supported by a degree in engineering or life sciences. Familiarity with tools like statistical process control (SPC) software, electronic quality management systems (eQMS), and documentation protocols is typical. Attention to detail, problem-solving abilities, and strong communication skills are essential soft skills for excelling in this role. These competencies are crucial for ensuring product safety, regulatory compliance, and maintaining the reputation of the medical device manufacturer.

What are some common challenges faced in a medical device quality control role, and how can I prepare for them?

Professionals in Medical Device Quality Control often face challenges such as keeping up with evolving regulatory standards, managing documentation for audits, and ensuring consistent product quality across batches. To prepare, it's helpful to develop strong attention to detail, stay updated on FDA and ISO guidelines, and build effective communication skills to collaborate with cross-functional teams like manufacturing and R&D. Being proactive in identifying potential risks and participating in continuous improvement initiatives can also help you succeed in this role.

What is the difference between Medical Device Quality Control vs Medical Device Quality Assurance?

AspectMedical Device Quality ControlMedical Device Quality Assurance
FocusInspecting and testing products to identify defectsDeveloping and maintaining quality systems and processes
ActivitiesProduct testing, inspection, samplingAudits, process validation, compliance management
CertificationsISO 13485, GMP trainingISO 13485, regulatory standards
Work EnvironmentLaboratories, manufacturing floorsQuality departments, regulatory offices

Medical Device Quality Control focuses on testing and inspecting products to ensure they meet quality standards, while Medical Device Quality Assurance emphasizes establishing systems and processes to prevent defects and ensure compliance. Both roles are essential in maintaining high-quality medical devices and often work closely within the industry.

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

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

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

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

What cities in Virginia are hiring for Medical Device Quality Control jobs?

Cities in Virginia with the most Medical Device Quality Control job openings:

Medical Device Quality Control jobs near you
Infographic showing various Medical Device Quality Control 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 $44,285 per year, or $21.3 per hour.

QA Manufacturing Engineer - Medical Device

Caraballo Consulting & Associates L

Sterling, VA • On-site

$40 - $80/hr

Contractor

Posted 16 days ago

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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.