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Director Quality Jobs in Virginia (NOW HIRING)

ATCC

Senior Director, Quality

Manassas, VA · On-site

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 ...

ATCC

Senior Director, Quality

Manassas, VA · On-site

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 ...

ATCC Biotechnology

Senior Director, Quality

Manassas, VA · On-site

$120 - $160/hr

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 ...

BeiGene USA

Associate Director, QC Microbiology

Hopewell, VA · On-site

$22.75 - $30/hr

Build a highly efficient QC microbiology team. Identify and develop key talents by mentoring, motivating, coaching direct reports to higher levels of capability. * Undertake any other duties as ...

Socket.dev

Quality / Safety Director

Chesapeake, VA · On-site

$149 - $201/hr

QEHS/SAFETY DIRECTOR Quality, Environmental, Health and Safety (QEHS) Responsible for planning and coordinating Quality, Environmental, Health and Safety (QEHS) activities with respect to GDIT ...

GDIT

Quality / Safety Director

Chesapeake, VA · On-site

QEHS/SAFETY DIRECTOR Quality, Environmental, Health and Safety (QEHS) Responsible for planning and coordinating Quality, Environmental, Health and Safety (QEHS) activities with respect to GDIT ...

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Director Quality information

See Virginia salary details

$30.7K

$124.5K

$211.7K

How much do director quality jobs pay per year?

As of Aug 21, 2026, the average yearly pay for director quality in Virginia is $124,523.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,200.00 and $149,700.00 per year, depending on experience, location, and employer.

What does a director of quality do?

A Director of Quality oversees the quality assurance and quality control processes within an organization to ensure that products or services meet established standards and regulatory requirements. They develop and implement quality management systems, lead teams responsible for inspections and audits, and work closely with other departments to promote continuous improvement. The Director of Quality also analyzes quality data, manages compliance with industry regulations, and often interacts with customers or external auditors to address quality concerns.

How does a director of quality typically collaborate with cross-functional teams to drive continuous improvement initiatives?

A Director of Quality plays a key role in partnering with departments such as manufacturing, engineering, supply chain, and regulatory affairs to identify and resolve process inefficiencies and ensure compliance with quality standards. They often lead cross-functional meetings, facilitate root cause analyses, and champion a culture of continuous improvement by implementing best practices and quality tools like Six Sigma or Lean methodologies. Effective communication and the ability to influence stakeholders at all levels are essential, as the Director of Quality ensures that all departments are aligned with organizational quality goals and regulatory requirements.

What are the key skills and qualifications needed to thrive as a director of quality, and why are they important?

To succeed as a Director of Quality, you need extensive knowledge in quality management systems, regulatory compliance, and process improvement, often supported by a bachelor's or master's degree in a relevant field. Familiarity with tools such as Six Sigma, ISO standards, and quality auditing software, along with certifications like CQE or Six Sigma Black Belt, is typical. Exceptional leadership, analytical thinking, and effective communication are critical soft skills for driving quality initiatives and leading cross-functional teams. These competencies ensure organizational standards are upheld, continuous improvement is achieved, and regulatory risks are minimized.

What is the difference between Director Quality vs Quality Manager?

AspectDirector QualityQuality Manager
CredentialsBachelor's or Master’s in Quality Management, Engineering, or related field; certifications like ASQ CQE or CQABachelor's in Quality, Engineering, or related; certifications like ASQ CQE or CQA often preferred
Work EnvironmentStrategic leadership in quality initiatives, overseeing multiple departments or sitesOperational focus, managing daily quality processes and teams
Employer & Industry UsageUsed in manufacturing, healthcare, aerospace, and industries with complex quality systemsCommon in manufacturing, production, and service industries

The main difference between a Director Quality and a Quality Manager lies in their scope and strategic focus. The Director Quality typically oversees the entire quality program at a higher level, setting policies and long-term goals, while the Quality Manager handles daily operations and implements quality procedures. Both roles require similar credentials and certifications, but their responsibilities and strategic influence differ significantly.

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

The most popular types of Quality jobs in Virginia are:

What are popular job titles related to Director Quality jobs in Virginia?

For Director Quality jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Director Quality jobs in Virginia look for?

The top searched job categories for Director Quality jobs in Virginia are:

What cities in Virginia are hiring for Director Quality jobs?

Cities in Virginia with the most Director Quality job openings:

Director Quality jobs near you
Infographic showing various Director Quality job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 20% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $124,523 per year, or $59.9 per hour.

Director Quality

Thermo Fisher Scientific

Middletown, VA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New

Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 428 frontline employees who took The Breakroom Quiz

175th of 543 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
As Director of Quality and Compliance, you will be responsible for taking a transformative approach to leading a dynamic and high-functioning Quality Assurance team at the Thermo Fisher Scientific, Clinical Diagnostics Division site in Middletown VA
The successful candidate will be responsible for raising the bar in process and culture across all aspects of quality system and compliance at the location, which performs development and manufacture of IVD products in adherence to applicable global regulations and standards such as US FDA QMSR, IVDD / IVDR, ISO13485:2016 (under MDSAP) and other GMP standards.
You will have responsibility for advising and collaborating with Manufacturing, Technical Operation and Commercial functions on quality and quality system requirements to ensure activities remain in compliance, and for driving continued evolution of the Quality function and site quality system to ensure it remains adequate to business needs and is successfully implemented.
This is a highly visible role at the site and Division level and, as a key member of the leadership team, you will report to the CDD Vice President, Global Quality Assurance & Regulatory Affairs.
A critical aspect of this role is serving as the primary quality representative for customers and regulatory authorities. As the site's Management Representative, the Director is responsible for ensuring the effectiveness of the Quality Management System and leading interactions during FDA inspections, MDSAP and ISO 13485 audits, and customer audits. This role requires strong leadership and communication skills to build customer confidence, maintain regulatory compliance, and represent Thermo Fisher Scientific with credibility and professionalism.
Key Responsibilities:
  • Acts as Management Representative of the Quality System and official correspondent of the site to all regulators (including US FDA). Primary contact at the site for all audits (regulator, Notified Body and customer).
  • Serve as a member of the site leadership team, providing strategic direction and influencing business decisions to ensure quality, compliance, and operational excellence are integrated into site objectives.
  • Establish strategies and drives actions to ensure the Quality Management System is adequate and successfully implemented to remain in sustained compliance with applicable regulations and standards.
  • Responsible for site product quality, compliance, conformance to quality requirements and specifications, and customer quality requirements. Supports regulatory recalls and interaction with government agencies.
  • Directly interacts with customers and OEM partners in relation to quality agreements, and quality matters associated with provided products and services.
  • Champion risk-based decision making by overseeing quality risk management processes and ensuring risks are identified, assessed, mitigated, and monitored throughout the product lifecycle.
  • Attracts, develops, and retains top talent to build an outstanding quality / regulatory function. Implements the required interpersonal structures and operating mechanisms to maintain appropriate oversight of the compliance status of the business and achieve results.
  • Grows and develops a customer-focused culture of personal quality in all site functions through leading, educating, and motivating site personnel using industry-leading practices.
  • Establishes and leads annual personnel resource and financial plans for the quality / regulatory organization.
  • Establishes annual site quality goals and objectives as part of annual Quality Improvement Plan and develops strategies and tactics to deliver associated results.
  • Leads and participates in cross functional teams for new product development, technology transfer, process improvement, and general operations.
  • Partners with regulatory affairs in all aspects of site regulatory processes that ensure the appropriate licensing, marketing and legal compliance of all appropriate diagnostics and medical device products globally.
  • Collaborate with global Quality and Regulatory leadership to standardize best practices, share lessons learned, and support enterprise quality initiatives.

Minimum Requirements/Qualifications:
  • A minimum of 10 years of quality / regulatory experience including at least 5 years of prior experience leading a quality / regulatory role.
  • Undergraduate degree in life science or biomedical engineering-related subject area preferred.
  • Strong demonstration of leadership capabilities required, with experience in driving organization and process change. Experience in leading transformations is preferred.
  • Strong solid understanding of QMS standards and medical device requirements/regulations (ISO 13485:2016 (preferably under MDSAP), US FDA QMSR, Health Canada, IVDD / IVDR)
  • Experienced in direct, professional interactions with customers and OEM business partners and regulatory authorities.
  • Ability to achieve results in a matrixed organization, using representatives from diverse cultures and embracing diversity.

Travel requirement:
  • <10% regional and international travel is expected.

Compensation and Benefits
The salary range estimated for this position based in Virginia is $145,500.00-$225,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs
  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement
  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
  • Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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