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Director Quality Jobs in Cave Spring, VA (NOW HIRING)

Quality Technician II

Blacksburg, VA · On-site

$15.75 - $21.25/hr

This role offers a great opportunity for someone who enjoys problem-solving, working cross-functionally, and making a direct impact on product quality and consumer safety. Primary Duties ...

Quality Engineer II

Salem, VA · On-site

$69K - $90K/yr

Quality - Customer Direct Complaint Rate, NCR rate, Complaint Cycle Time, CAPA Cycle Time ... Innovation and ideation are critical aspects of your role, and you will be expected to generate ...

Quality - Customer Direct Complaint Rate, NCR rate, Complaint Cycle Time, CAPA Cycle Time ... Innovation and ideation are critical aspects of your role, and you will be expected to generate ...

Clinic Director

Roanoke, VA · On-site

$95K - $120K/yr

As a Clinic Director , you'll oversee clinical operations across multiple clinic locations while mentoring and developing BCBA teams, driving clinical excellence, and ensuring high-quality, ethical ...

The Director of Clinical Services also establishes, implements and evaluates goals and objectives for hospice services that meet and promote the standards of quality and contribute to the total ...

If you're motivated to give our clients a more positive quality of life, we encourage you to apply today! Responsibilities * Assist State Director with review and updates of department materials such ...

Medical Director

Roanoke, VA · On-site

$218K - $272K/yr

We are seeking a dedicated Hospice Medical Director to join our leadership team and provide expert ... Oversee and ensure quality medical services delivered by hospice physicians across multiple ...

Experience with staff management, scheduling, budgeting, and quality improvement * Strong knowledge ... Director-level nursing leadership experience * Correctional healthcare experience * Knowledge of ...

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Showing results 1-20

Director Quality information

See Cave Spring, VA salary details

$27.2K

$110.4K

$187.6K

How much do director quality jobs pay per year?

As of Aug 24, 2026, the average yearly pay for director quality in Cave Spring, VA is $110,353.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,000.00 and $132,700.00 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 cities near Cave Spring, VA are hiring for Director Quality jobs?

Cities near Cave Spring, VA with the most Director Quality job openings:

Infographic showing various Director Quality job openings in Cave Spring, VA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, 5% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $110,353 per year, or $53.1 per hour.

Quality Supervisor

Traditional Medicinals

Rocky Mount, VA • On-site

Full-time

Posted 5 days ago


Job description

SUMMARY
The Quality Supervisor supervises Quality staff in their day-to-day responsibilities. Ensures in-process quality functions are executed, and manufacturing operations are in compliance with company policies, procedures, and applicable cGMP requirements. Ensures timely disposition of incoming ingredients, component, blends, and finished goods. This position also ensures lab activities are compliant, accurate and documented.
ESSENTIAL FUNCTIONS
  • Supervise day-to-day activities and training of Quality department personnel including quality inspectors and laboratory personnel.
  • Ensure timely and accurate inspection, testing and disposition of QC samples (e.g., components, ingredients, blends, finished products, pre-ship samples, retest materials, R&D materials)
  • Ensure all lab instrumentation/equipment is functioning properly, validated for use, and appropriately scheduled for preventative maintenance and calibration
  • Lead OOS investigations with focus on identifying root causes and taking corrective action where appropriate; document and communicate non-conformances to stakeholders
  • Ensure accuracy and completeness of documentation (e.g., batch records, evaluation forms, deviations, NCMRs, Corrective Actions, including electronic/digital records)
  • Partner with Production, Research & Development, Procurement and Planning, and other departments to understand production or corporate priorities and adjust personnel and department priorities as needed
  • Ensure that processes and methods utilized in the laboratory are compliant and accurate
  • Ensure that department personnel are properly trained and qualified to perform their job
  • Ensure compliance with current company, departmental and regulatory requirements
  • Ongoing assessment of facility operations considering continuous improvement
  • Assists and performs data collection and analysis of QC metrics
  • Generates or revises controlled documents such as SOPs and data forms
  • Lead for special projects as assigned
  • Perform maintenance, data entry, and analysis in various electronic systems utilized by the company
  • Perform Quality Inspector duties as backup when needed
  • Site QMS systems subject matter expert (e.g. Redzone, Master Control, Ignition, etc.)
  • Other duties as assigned
SUPERVISORY/BUDGET
  • Direct supervision of Quality department inspectors and lab technicians
  • No direct budgetary oversight
REQUIREMENTS
Education and Experience:
  • BA or BS in scientific discipline or equivalent education/experience
  • Two years' Quality experience in a regulated industry
  • Four years' hands-on QC or analytical chemistry experience in a regulated industry
  • 2+ year supervisory experience in a comparable setting
  • Project management experience preferred
Knowledge/Abilities/Skills:
  • Strong knowledge of cGMP requirements and quality systems within a regulated industry, such as food, dietary supplements, cosmetics, or pharmaceuticals, required. Knowledge of regulatory requirements for dietary supplements (21 CFR Part 111) preferred.
  • Technical proficiency in analytical methodologies
  • Strong knowledge of laboratory protocols and equipment
  • Demonstrated ability to manage and develop staff
  • Able to collaborate, influence and work effectively across multiple departments
  • Ability to read and interpret regulatory documents
  • Able to independently solve problems and make decisions based on company and/or quality policy
  • Ability to effectively manage competing priorities with the drive and ability to meet deadlines
  • Excellent organization skills and attention to detail
  • Strong verbal and written communication skills
  • Commitment to and ability to demonstrate TM's Company values: humility, respect, quality, collaboration, innovation and sustainability
Technical Skills:
  • Intermediate MS Suite
  • WMS/ERP systems preferred
Travel Requirements:
  • Occasional travel to California or 3rd party test labs or supplier(s)
Work Environment:
  • Works often in the QC laboratory with hazardous chemicals present, requiring competence and familiarity with safe handling and storage of acids, bases and solvents.
  • Works often in production area(s)warehouse, must follow GMP requirements and safety precautions for each area.