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Capa Jobs in Virginia (NOW HIRING)

Maintain and enhance core quality processes including CAPA, deviations, change control, and audits, consistent with applicable ISO standards and other relevant regulatory guidelines. * Quality ...

Associate Manager, R&D

Leesburg, VA · On-site

$125K - $135K/yr

Mentor others on industry standards, design requirements, test strategies, design controls, risk management, and NC/CAPA processes * Identify and implement improvements to reduce cost, increase ...

Maintain and enhance core quality processes including CAPA, deviations, change control, and audits, consistent with applicable ISO standards and other relevant regulatory guidelines. * Quality ...

Lead enterprise root cause analysis, CAPA, risk management, and quality improvement initiatives using Lean and Six Sigma methodologies. * Ensure compliance with applicable regulatory, customer, and ...

Quality Engineer

Norfolk, VA · On-site

$69K - $90K/yr

Knowledge and experience with quality tools, such as CAPA, six sigma, lean manufacturing, PPAP, FMEA, problem solving techniques, and root cause analysis. * Participate in APQP and NPI activities

QA Associate - Laboratory

Richmond, VA · On-site

$20 - $23/hr

Track CAPA and perform or assist with Root Cause Analysis (RCA). * Conduct routine internal audits of laboratory processes, documentation, and facilities. * Prepare audit checklists, reports, and ...

Quality Control Engineer

Chester, VA · On-site

$69K - $103K/yr

Strong problem-solving skills and experience with root cause analysis and CAPA. * Familiarity with quality system standards such as ISO 9001, GMP, or ISO 17025. * Excellent communication and ...

Showing results 41-60

Capa information

What are the typical daily responsibilities of a CAPA specialist?

A CAPA specialist is responsible for investigating quality issues, identifying root causes, and implementing corrective and preventive actions to ensure ongoing compliance and product integrity. Their typical day involves reviewing nonconformance reports, collaborating with cross-functional teams, documenting findings, and tracking the progress of CAPA initiatives using specialized software. CAPA specialists also prepare reports for audits and may facilitate meetings to drive continuous improvement activities. This role often requires balancing multiple projects and deadlines in a regulated environment, making organizational and communication skills crucial for success.

What are the key skills and qualifications needed to thrive in the CAPA position, and why are they important?

To thrive as a CAPA (Corrective and Preventive Action) specialist, you need expertise in quality management systems, root cause analysis, and compliance with industry standards, typically backed by a degree in engineering, life sciences, or a related field. Familiarity with CAPA software, regulatory frameworks (such as ISO 13485 or FDA 21 CFR Part 820), and document control systems is essential. Strong analytical thinking, attention to detail, and effective communication skills are vital soft skills for this role. These skills ensure effective problem-solving and sustained compliance, which are essential for maintaining product quality and meeting regulatory requirements.

What is a CAPA?

A CAPA (Corrective and Preventive Action) job involves identifying, investigating, and resolving quality issues in industries like manufacturing, healthcare, and pharmaceuticals. CAPA professionals analyze root causes of defects or process failures and implement corrective actions to prevent recurrence. They ensure compliance with regulatory standards, document findings, and improve overall quality management systems. Their role is critical in maintaining product safety, efficiency, and regulatory adherence.

What are the most commonly searched types of Capa jobs in Virginia? The most popular types of Capa jobs in Virginia are:
What are popular job titles related to Capa jobs in Virginia? For Capa jobs in Virginia, the most frequently searched job titles are:
Infographic showing various Capa job openings in Virginia as of August 2026, with employment types broken down into 82% Full Time, 8% Part Time, 1% Temporary, 8% Contract, and 1% Nights. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution.

Senior Director, Quality

ATCC

Manassas, VA

Full-time

Medical, Life, Retirement, PTO

Re-posted 12 days ago


Job description

Ready to shape the future of science and global health? A global nonprofit that provides trusted biological materials for science and health, ATCC is hiring a Senior Director, Quality to provide enterprise leadership for ATCC’s Quality organization, ensuring compliance with applicable regulations and industry standards. Reporting to the Chief Operating Officer, this leader will oversee a team of up to 60 FTE across Quality Control, Quality Systems, Operations Quality, Validation, and External Supplier Quality, supporting regulated bioproduction of commercial catalog products and critical services for industry and government. ATCC is ISO 9001 and ISO 13485 certified and ISO/IEC 17025 and ISO 17034 accredited, with a mission-driven focus on excellence in quality.

This is a highly visible leadership role responsible for advancing enterprise-wide quality performance, strengthening operational integration, and ensuring consistent quality and compliance across manufacturing and service delivery, in close partnership with internal and external stakeholders. This is an onsite position based fully in Manassas, VA or split between our Manassas, VA and Gaithersburg, MD facilities. 


  • Quality Management System (QMS): Provide strategic and scientific leadership for the organization’s risk-based QMS, ensuring compliant, controlled documentation and sustained inspection/audit readiness. Maintain and enhance core quality processes including CAPA, deviations, change control, and audits, consistent with applicable ISO standards and other relevant regulatory guidelines.
  • Quality Assurance Across Operations: Lead and oversee Quality Assurance functions supporting BioProduction, ATCC Federal Services, Supply Chain, Facilities, and operational teams, embedding Quality within operations and facilities using a risk-based, science-based approach.
  • QC Laboratory Operations & Release: Oversee QC laboratory operations, including method validation and release testing, ensuring consistent product disposition decisions and compliance with applicable standards.
  • Validation & Data Integrity: Provide oversight of validation programs (CSV, equipment, and process validation) and ensure data integrity principles are embedded across validated systems and processes in line with guidelines. 
  • Supplier Quality & Regulatory Compliance: Oversee supplier quality and external partner compliance, including partnership on the start-up of ATCC's new facility in Manassas.
  • Leadership & Culture: Build and lead high-performing teams, embedding a culture of quality through coaching, training, and cross-functional partnership across scientific and operational groups.  Proactively partner with R&D, Operations, Supply Chain functions to continuously evaluate and optimize delivery of both Quality and on-time delivery of manufacturing and services.

  • Minimum Requirement: PhD and 11 years, including 2 years of supervisory experience or equivalent experience (Master’s and 16 years, Bachelor’s and 18 years, or HS Diploma and 22 years).
  • Progressive Quality leadership experience in ISO- or GMP-compliant organizations providing biologics products and services.
  • Demonstrated autonomy to lead a large, multi-functional Quality organization, drive enterprise-wide quality strategy, and partner with executive and operational stakeholders in a regulated manufacturing environment.
  • Expertise in ISO 13485, ISO 9001, ISO/IEC 17025, and ISO 17034, with strong command of quality systems expectations and audit execution.  Proven track record of engaging external stakeholders as relevant for biologics quality operations.
  • Experience managing multi-functional Quality organizations spanning QMS, QC, validation, and supplier quality with measurable outcomes. Experience with oversight of multiple sites and R&D and manufacturing is a plus.
  • Demonstrated experience overseeing QC laboratory operations, method validation, and release testing for biological materials.
  • Strong capability in CAPA, deviation management, change control, risk management, controlled documentation, validation oversight (CSV/equipment/process), and data integrity.
  • Preferred: Experience supporting quality requirements and facility start-up operations.
  • Preferred: PhD and/or educational background in biology or related life sciences field.

We Invest in You 

 

  • Health & Wellness: 
    • Comprehensive medical coverage and company paid Life Insurance, Disability Insurance, AD&D, and paid parental leave
    • Work life balance with Paid Holidays and PTO
    • Fitness and cell phone subsidies, and additional benefits such as legal services, pet insurance and additional supplemental coverage.  
    • Employee Assistance Program offering around-the-clock counseling
  • Financial security: 
    • 401(a) (6% employer contribution) and 403(b) (2% match) retirement plans
    • Exceptional career advancement opportunities, recognition, and rewards
    • Corporate bonus program
  • Mission Focused:
    • Non-profit organization supporting critical life science research
    • We give scientists the tools they need to make discoveries that improve and save lives
    • Contribute to community involvement and social responsibility

Join ATCC, where we fuel your success, well-being, and development. We're a mission-focused non-profit Equal Opportunity Employer, celebrating a century of supporting global public health.  All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.  Shape the future of science with us.