Quality Control Manager Jobs in Virginia
Quality Control Manager jobs in Virginia are in active demand, concentrated in defense contracting, federal government supply chains, food and beverage manufacturing, and life sciences, with openings at every level from entry-level QC coordinator through senior quality director. The busiest hiring metros are Northern Virginia, Richmond, and Hampton Roads, where major employers such as Northrop Grumman, Altria Group, and Huntington Ingalls Industries maintain longstanding quality operations. The most sought-after specialties in Virginia are defense systems quality assurance, ISO and AS9100 compliance management, and pharmaceutical and biotech QC. Find a role that fits below and apply directly.
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Position Summary
The Senior QC Chemist performs and oversees CGMP laboratory testing of raw materials, in-process and finished products, and stability samples using approved and validated methods. The role supports analytical method transfer, validation, and improvement; investigates OOS/OOT and atypical results; ensures data integrity and inspection readiness; provides technical guidance; and collaborates with QA, Manufacturing, Validation, and other teams to support product quality and timely release.
Responsibilities:
- Analytical testing: Perform routine and complex chemical testing of raw materials, in-process samples, finished products, stability samples, and process-related materials using approved procedures, compendial methods, and validated analytical methods.
- Instrumentation: Operate, troubleshoot, and maintain laboratory instruments such as HPLC, GC, UV-Vis, FTIR, dissolution, Karl Fischer, pH, conductivity, and other applicable analytical equipment.
- Method lifecycle support: Support analytical method transfer, verification, validation, optimization, and continuous improvement; draft or revise protocols, reports, specifications, and test methods as assigned.
- Data review: Review analytical data, calculations, chromatograms, laboratory notebooks, worksheets, and electronic records for accuracy, completeness, compliance, and conformance to specifications.
- Laboratory investigations: Lead or support investigations of atypical, out-of-specification, out-of-trend, and laboratory-error results; document scientifically sound root-cause assessments and support corrective and preventive actions.
- Stability and release support: Execute testing according to approved release and stability schedules, evaluate results against established acceptance criteria, and promptly communicate issues that may affect product disposition or timelines.
- Documentation and data integrity: Complete records contemporaneously and accurately in accordance with CGMP, ALCOA+ principles, laboratory procedures, and applicable electronic data systems.
- Equipment and laboratory controls: Ensure instruments are calibrated, qualified, and maintained; manage standards, reagents, columns, and laboratory supplies in accordance with approved requirements.
- Technical leadership: Provide technical guidance and training to QC analysts and chemists, promote consistent laboratory practices, and serve as a subject-matter resource for analytical methods and instrumentation.
- Compliance and collaboration: Maintain inspection readiness, participate in audits and regulatory inspections, and collaborate with Quality Assurance, Manufacturing, Validation, Engineering, and other functions to resolve technical issues and support laboratory priorities.
Qualifications and Requirements
- Bachelor's degree in chemistry, biochemistry, pharmaceutical sciences, or a related scientific discipline; an advanced degree is a plus.
- Six or more years of progressive analytical laboratory experience, including at least 6 years in a CGMP-regulated pharmaceutical, or related environment.
- Demonstrated hands-on experience with chromatographic and spectroscopic techniques, including HPLC and one or more of GC, UV-Vis, FTIR, dissolution, Karl Fischer, pH, or conductivity testing.
- Experience with compendial testing and analytical method transfer, verification, validation, troubleshooting, or optimization.
- Working knowledge of CGMP, USP or other applicable compendia, FDA expectations, data-integrity requirements, laboratory safety, and GDP.
- Experience investigating atypical, out-of-specification, and out-of-trend results and supporting scientifically sound root-cause analysis and corrective actions.
- Proficiency with laboratory information management systems, chromatography data systems, electronic document systems, and Microsoft Office applications preferred.
Strong technical writing, analytical problem-solving, organization, communication, and mentoring skills, with the ability to manage competing priorities independently in a fast-paced
Pay: From $90,000.00 per year
Benefits:
- 401(k) matching
- Dental insurance
- Employee assistance program
- Health insurance
- Life insurance
- Paid time off
Work Location: In person
Position Summary
The Senior QC Chemist performs and oversees CGMP laboratory testing of raw materials, in-process and finished products, and stability samples using approved and validated methods. The role supports analytical method transfer, validation, and improvement; investigates OOS/OOT and atypical results; ensures data integrity and inspection readiness; provides technical guidance; and collaborates with QA, Manufacturing, Validation, and other teams to support product quality and timely release.
Responsibilities:
- Analytical testing: Perform routine and complex chemical testing of raw materials, in-process samples, finished products, stability samples, and process-related materials using approved procedures, compendial methods, and validated analytical methods.
- Instrumentation: Operate, troubleshoot, and maintain laboratory instruments such as HPLC, GC, UV-Vis, FTIR, dissolution, Karl Fischer, pH, conductivity, and other applicable analytical equipment.
- Method lifecycle support: Support analytical method transfer, verification, validation, optimization, and continuous improvement; draft or revise protocols, reports, specifications, and test methods as assigned.
- Data review: Review analytical data, calculations, chromatograms, laboratory notebooks, worksheets, and electronic records for accuracy, completeness, compliance, and conformance to specifications.
- Laboratory investigations: Lead or support investigations of atypical, out-of-specification, out-of-trend, and laboratory-error results; document scientifically sound root-cause assessments and support corrective and preventive actions.
- Stability and release support: Execute testing according to approved release and stability schedules, evaluate results against established acceptance criteria, and promptly communicate issues that may affect product disposition or timelines.
- Documentation and data integrity: Complete records contemporaneously and accurately in accordance with CGMP, ALCOA+ principles, laboratory procedures, and applicable electronic data systems.
- Equipment and laboratory controls: Ensure instruments are calibrated, qualified, and maintained; manage standards, reagents, columns, and laboratory supplies in accordance with approved requirements.
- Technical leadership: Provide technical guidance and training to QC analysts and chemists, promote consistent laboratory practices, and serve as a subject-matter resource for analytical methods and instrumentation.
- Compliance and collaboration: Maintain inspection readiness, participate in audits and regulatory inspections, and collaborate with Quality Assurance, Manufacturing, Validation, Engineering, and other functions to resolve technical issues and support laboratory priorities.
Qualifications and Requirements
- Bachelor's degree in chemistry, biochemistry, pharmaceutical sciences, or a related scientific discipline; an advanced degree is a plus.
- Six or more years of progressive analytical laboratory experience, including at least 6 years in a CGMP-regulated pharmaceutical, or related environment.
- Demonstrated hands-on experience with chromatographic and spectroscopic techniques, including HPLC and one or more of GC, UV-Vis, FTIR, dissolution, Karl Fischer, pH, or conductivity testing.
- Experience with compendial testing and analytical method transfer, verification, validation, troubleshooting, or optimization.
- Working knowledge of CGMP, USP or other applicable compendia, FDA expectations, data-integrity requirements, laboratory safety, and GDP.
- Experience investigating atypical, out-of-specification, and out-of-trend results and supporting scientifically sound root-cause analysis and corrective actions.
- Proficiency with laboratory information management systems, chromatography data systems, electronic document systems, and Microsoft Office applications preferred.
Strong technical writing, analytical problem-solving, organization, communication, and mentoring skills, with the ability to manage competing priorities independently in a fast-paced
Pay: From $90,000.00 per year
Benefits:
- 401(k) matching
- Dental insurance
- Employee assistance program
- Health insurance
- Life insurance
- Paid time off
Work Location: In person
See All 86 Quality Control Manager Jobs in Virginia
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Find Quality Control Manager JobsQuality Control Manager Jobs by City in Virginia
Where Virginia roles are concentrated, by current openings.
Quality Control Manager Job Market in Virginia
A snapshot from current Virginia openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Staffing & Recruiting
- Construction & Real Estate
- Manufacturing
- Science & Research
- Electronics & Hardware
What Virginia Employers Look For
The qualifications that appear most often in quality control manager jobs across Virginia.
- Bachelor's degree in engineering, science, or a related technical field required
- Five or more years of quality control or quality assurance experience in a relevant industry
- Demonstrated knowledge of ISO 9001, AS9100, or IATF 16949 quality management standards
- Experience managing audits, corrective actions, and supplier quality programs
- Proficiency with statistical process control tools and quality management software
- Certified Quality Manager or Certified Quality Engineer credential from ASQ preferred
Quality Control Manager Jobs in Virginia: Frequently Asked Questions
How do you become a quality control manager in Virginia?
Becoming a quality control manager in Virginia typically starts with a bachelor's degree in engineering, manufacturing, life sciences, or a related technical field. Virginia does not require a state-issued license for most quality control manager roles, but employers in defense, aerospace, and pharma strongly prefer candidates with an ASQ Certified Quality Manager or Certified Quality Engineer credential. Gaining experience in auditing, process improvement, or QC coordination at Virginia's defense contractors or manufacturing firms builds the clearest path to a management role.
How much do quality control managers make in Virginia?
Quality control managers in Virginia earn a median of about $128,230 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $83,390 for the lowest 10% to over $206,820 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire quality control managers in Virginia?
Employers hiring quality control managers in Virginia right now include Jobot, Ameritek, and EXTREME STEEL, based on current listings on Migrate Mate as of September 2026. Virginia's heavy concentration of defense contractors, federal government suppliers, and food and pharmaceutical manufacturers means demand for quality management professionals stays consistent throughout the year.
Which Virginia cities have the most quality control manager jobs?
The cities with the most quality control manager openings in Virginia are Richmond, Sterling, and Norfolk. Northern Virginia drives volume through its dense cluster of defense contractors and federal agency suppliers, Richmond anchors food, beverage, and pharmaceutical manufacturing hiring, and Hampton Roads supports steady demand through its major shipbuilding and military logistics operations.
Are there remote quality control manager jobs in Virginia?
Yes, but they are rare. Quality control management is largely a hands-on, facility-based role requiring physical inspection, audit oversight, and direct supervision of production or lab environments, so most positions require on-site presence. About 0% of quality control manager openings tied to Virginia are remote or hybrid as of September 2026. The portions of the role most suited to remote work include document control, supplier audit coordination, and quality system reporting.
How can I get hired as a quality control manager in Virginia with little or no experience?
The most realistic entry path is moving into a quality control inspector, quality technician, or process technician role at a Virginia manufacturing or defense facility, then building toward management. Large Northern Virginia defense contractors and Richmond-area food manufacturers regularly hire entry-level QC technicians and offer internal advancement. Earning an ASQ Certified Quality Improvement Associate credential while in an early role signals readiness for management. Adjacent roles in production supervision or supply chain coordination at the same employers also provide a recognized route into quality management.
Where can I find and apply to quality control manager jobs in Virginia?
You can find and apply to quality control manager jobs in Virginia on Migrate Mate, which lists current Virginia openings across defense, manufacturing, life sciences, and food production. Find roles that fit your experience and apply directly to the employers posting them.
See All 86 Quality Control Manager Jobs in Virginia
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