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Director Quality Engineer Fda Jobs in Virginia (NOW HIRING)

Sr. Quality Engineer

Leesburg, VA · On-site

$100K - $110K/yr

Senior Quality Engineer Location: Leesburg, VA Company: VB Spine Looking for a career where your ... Experience interacting with regulatory agencies and supporting audits (FDA, Notified Bodies, etc.

Quality Engineer I

Virginia Beach, VA

$64K - $83K/yr

Quality Engineering Schedule : Monday-Friday | 8:15AM - 5:00PM Clinical Status : Clinical HOW YOU ... FDA 21 CFR Part 820, 21 CFR Part 1271 , ISO 13485, and ISO 14971. This role will also play a ...

Quality Engineer I

Virginia Beach, VA

$64K - $83K/yr

Quality Engineering Schedule: Monday-Friday | 8:15AM - 5:00PM Clinical Status: Clinical HOW YOU'LL ... FDA 21 CFR Part 820, 21 CFR Part 1271, ISO 13485, and ISO 14971. This role will also play a ...

Quality Engineer I

Virginia Beach, VA

$68K - $88K/yr

Quality Engineering Schedule: Monday-Friday | 8:15AM - 5:00PM Clinical Status: Clinical HOW YOU'LL ... FDA 21 CFR Part 820, 21 CFR Part 1271, ISO 13485, and ISO 14971. This role will also play a ...

Quality Engineer I

Virginia Beach, VA · On-site

$68K - $88K/yr

Quality Engineering Schedule: Monday-Friday 8:15AM - 5:00PM Clinical Status: Clinical HOW YOU'LL ... FDA 21 CFR Part 820, 21 CFR Part 1271, ISO 13485, and ISO 14971. This role will also play a ...

Quality Engineer II

Salem, VA · On-site

$69K - $90K/yr

Food and Drug Administration (FDA) regulations, company policies and operating procedures, and ... Quality - Customer Direct Complaint Rate, NCR rate, Complaint Cycle Time, CAPA Cycle Time

Quality Engineer II

Salem, VA · On-site

$69K - $90K/yr

Food and Drug Administration (FDA) regulations, company policies and operating procedures, and ... Quality - Customer Direct Complaint Rate, NCR rate, Complaint Cycle Time, CAPA Cycle Time

Quality Engineer - Mobile Travel Team

Ashburn, VA · On-site

$73K - $95K/yr

... the FDA. Has the responsibility to lead audits as well as serve as the primary quality ... Prepares and delivers performance appraisal to direct reports. Mentors and coaches team members to ...

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Showing results 1-20

Director Quality Engineer Fda information

What is the difference between Director Quality Engineer Fda vs Quality Engineer Fda?

AspectDirector Quality Engineer FdaQuality Engineer Fda
CredentialsTypically requires a Bachelor's degree in Engineering or Life Sciences, with certifications like ASQ CQE or ISO auditorRequires similar degrees and certifications, often entry to mid-level
Work EnvironmentLeads quality teams, oversees compliance, and strategic planning in manufacturing or biotech settingsPerforms hands-on quality testing, inspections, and process improvements
Industry UsageCommonly used in regulated industries like pharmaceuticals, biotech, and medical devicesUsed across manufacturing, biotech, and pharmaceutical companies for quality assurance

The main difference is that the Director Quality Engineer Fda holds a leadership role with strategic responsibilities, overseeing quality systems and compliance, while the Quality Engineer Fda focuses on operational quality tasks and testing. Both roles require similar credentials but differ in scope and seniority.

What are the most commonly searched types of Quality Engineer Fda jobs in Virginia?

The most popular types of Quality Engineer Fda jobs in Virginia are:

What cities in Virginia are hiring for Director Quality Engineer Fda jobs?

Cities in Virginia with the most Director Quality Engineer Fda job openings:

Infographic showing various Director Quality Engineer Fda job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution.

Senior Quality Assurance Engineer, Medical Devices

Pop-Up Talent

Charlottesville, VA • On-site

$75K - $105K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 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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