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Director Quality Compliance Jobs (NOW HIRING)

Quala

Air Quality Compliance Director

Tampa, FL · On-site +1

$120K - $140K/yr

In support of the Senior Director of EHS Compliance, the Air Quality Compliance Leader is responsible for the Air Quality Program at Depot Connect International (DCI). The Air Quality Compliance ...

Quala

Air Quality Compliance Director

Houston, TX · On-site +1

$120K - $140K/yr

In support of the Senior Director of EHS Compliance, the Air Quality Compliance Leader is responsible for the Air Quality Program at Depot Connect International (DCI). The Air Quality Compliance ...

Scentbird

Director of Quality & Compliance

Somerset, NJ · On-site

Director of Quality & Compliance About the Role: The Director of Quality & Compliance is responsible for leading the company's Quality Management System (QMS) and ensuring the consistent delivery of ...

TERUMO BCT, INC

$120 - $170/hr

Director, Global Quality & Compliance Date: Aug 19, 2026 Location: Lakewood, CO, US Requisition ID: 35415 At Terumo Blood and Cell Technologies, our 8,000+ global associates proud to come to work ...

Choiceorganicteas

Quality Compliance Manager

Eugene, OR · On-site

$90 - $110/hr

Quality Compliance Manager Full Time Regular Professional Eugene, OR, US 3 days ago Requisition ID ... Report to the Quality Manager and Director Quality on the state of the specialist team's functions ...

New

Yogi Tea

Quality Compliance Manager

Eugene, OR · On-site

$90 - $120/hr

Quality Compliance Manager Full Time Regular Professional Eugene, OR, US 7 days ago Requisition ID ... Report to the Quality Manager and Director Quality on the state of the specialist team's functions ...

New

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Director Quality Compliance information

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$31K

$125.6K

$213.5K

How much do director quality compliance jobs pay per year?

As of Sep 3, 2026, the average yearly pay for director quality compliance in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

What does a director quality compliance do?

A Director of Quality Compliance is responsible for overseeing and ensuring that an organization adheres to regulatory standards and internal policies related to quality. This role involves developing and maintaining quality management systems, leading audits, and coordinating with various departments to implement compliance initiatives. The director also monitors changes in regulations, addresses non-compliance issues, and provides training to staff. Their ultimate goal is to ensure products or services consistently meet both customer expectations and legal requirements.

What are the key skills and qualifications needed to thrive as a director quality compliance?

To excel as a Director of Quality Compliance, you need deep expertise in quality management systems, regulatory requirements, and risk assessment, often backed by a relevant degree and experience in compliance roles. Familiarity with industry standards (such as ISO 9001 or FDA regulations), auditing software, and compliance management tools is typically required. Outstanding leadership, attention to detail, and strong communication skills help drive organizational adherence to standards and foster a culture of quality. These competencies are essential to ensure regulatory compliance, minimize risks, and maintain organizational reputation in a highly regulated environment.

What are some common challenges faced by a director quality compliance, and how can they be addressed?

Directors of Quality Compliance often face challenges such as keeping up with evolving regulations, ensuring organization-wide adherence to quality standards, and fostering a culture of continuous improvement. Balancing regulatory requirements with operational efficiency and communicating compliance expectations across diverse teams can also be difficult. Success in this role typically involves staying informed about industry changes, implementing robust training programs, and collaborating closely with cross-functional stakeholders to drive quality initiatives. Establishing clear processes and open channels for feedback can help proactively identify and resolve compliance issues.

What is the difference between Director Quality Compliance vs Quality Manager?

AspectDirector Quality ComplianceQuality Manager
CertificationsISO 9001 Lead Auditor, ASQ certificationsISO 9001 Lead Auditor, ASQ certifications
Work EnvironmentStrategic oversight, executive collaborationOperational management, team supervision
Employer & Industry UsageManufacturing, healthcare, aerospaceManufacturing, pharmaceuticals, automotive
Search & Comparison IntentFocus on compliance strategy and policyFocus on daily quality operations

The main difference is that the Director Quality Compliance oversees compliance strategies and policies at an executive level, while the Quality Manager handles daily quality operations and team management. Both roles require similar certifications but differ in scope and strategic focus.

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Director Quality Compliance jobs near you
Infographic showing various Director Quality Compliance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Director of Quality & Compliance

The O'Connor Group

Conshohocken, PA • On-site

Full-time

Re-posted 28 days ago

Job description

We are partnering with our client, Active Protective Technologies, to hire a Director of Quality & Compliance!
About Active Protective Technologies:
Active Protective Technologies is a medical device startup committed to revolutionizing the treatment of older adults at risk of a fall-induced hip fracture due to diagnosed osteoporosis and fall risk. Our flagship product, the Tango Belt, integrates cutting-edge technology into a wearable device that detects a serious hip-impacting fall in progress and deploys an airbag at the hips to attenuate impact force and mitigate fall-induced major hip injury, a leading cause of disability and death in older adults. The Tango® Belt was designated a Breakthrough Device by the FDA to recognize its potential to significantly improve the standard of care for this debilitating condition. The FDA granted us De Novo authorization to begin marketing the Tango Belt in April 2025, and US commercialization is underway. For more info on our mission and product, please visit www.tangobelt.com .
Job Overview:
Active Protective seeks a Quality & Compliance Director with both industry-standard technical skills and an attitude to contribute to a collaborative, positive work environment. In this role the Quality & Compliance Director is ultimately responsible to meet compliance requirements for the business, under both Food & Drug Administration and Centers for Medicare Services. Quality & Compliance Director directly oversees Quality Management Systems, Regulatory/Compliance, directing employees as needed, and works cross-functionally with Executive, Engineering, Information Technology, Clinical, Finance, Human Resources, and Commercialization personnel.
Key Responsibilities:
  • Regulatory Affairs: Maintain compliance with U.S. Food & Drug Administration requirements, serving as the operational owner for all required registrations and licenses, regulatory readiness, government audits, and corrective actions. Represent Regulatory Affairs within the Product Development team. Chiefly responsible for compliance of all product labeling, instructions for use, and marketing claims. Work cross functionally with Engineering, Clinical & Marketing.
  • Quality Management Systems: Oversee the Quality Management System in accordance with ISO 13485 and FDA Quality System Regulation (21 CFR 820), including document control, audits, non-conformance, complaint handling, quality inspections, CAPA, and continuous improvement. Represent Quality within the Product Development team. Work with Engineering regarding issues related to product design and defects; work with all other cross-functional groups as needed to ensure implementation of compliant procedure.
  • Durable Medical Equipment Program Compliance: Work cross-functionally to ensure Durable Medical Equipment (DME) program compliance with Medicare DMEPOS supplier standards, accreditation, and Medicare requirements.
  • HIPAA Compliance Program: Work cross-functionally with Information Technology, Software Engineering, Clinical and Commercial Operations to ensure compliance with HIPAA requirements for the safeguarding of protected health information (PHI), protecting company and customer data, and maintaining system integrity.
  • Health & Safety Program Compliance: Work cross functionally with Facilities, Product Operations and Human Resources to provide a safe, secure, work environment in compliance with OSHA, Medicare and FDA standards.
  • Government & Legal Affairs: Directly oversee legal and government affairs operations. Maintain connections with key trade groups, lobbying groups and government officials. Support review of company contracts, terms & conditions, and official statements, working with external counsel as needed.
  • Continuous Improvement: Establish, monitor, and improve work processes and outputs under assigned responsibilities.

Qualifications:
  • Education: Bachelor's degree in engineering or scientific discipline; Compliance certifications are a plus;
  • Experience: Minimum of 10 years of experience in an FDA or CMS regulated space;
  • Personal Skills: Strong communication skills, both written and verbal. Strong ability to work collaboratively and cross-functionally with team members, and to work under business direction.
  • Technical Skills:
    • Strong organizational skills a must.
    • Strong attention to detail is a must.
    • Strong knowledge of FDA requirements and quality management principles (ISO 13485).
    • Strong knowledge of Medicare Durable Medical Equipment requirements.
    • Proficiency with relevant software (e.g. eQMS, word processing, etc.)
  • Knowledge: Strong understanding of medical device quality, logistical and manufacturing processes, quality assurance practices, and industry standards.

Physical Requirements:
  • Must be present 2 days per week in-office, and available in office as needed.
  • Must be available for business travel (e.g. supplier visits) as needed.
  • Must have no violations of Medicare or HIPAA.

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