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Director Quality Compliance Jobs (NOW HIRING)

Cellares

Director, Quality Compliance

Bridgewater, NJ · On-site

$90K - $250K/yr

We are seeking an innovative and highly motivated Director, Quality Compliance, who will contribute significantly to the growth of the Cellares team. This individual will be responsible for leading ...

Cellares

Director, Quality Compliance

Bridgewater, NJ

$90K - $250K/yr

We are seeking an innovative and highly motivated Director, Quality Compliance, who will contribute significantly to the growth of the Cellares team. This individual will be responsible for leading ...

Cellares

Director, Quality Compliance

Bridgewater, MA · On-site

$90 - $210/hr

We are seeking an innovative and highly motivated Director, Quality Compliance to lead the quality compliance activities for the Bridgewater site. The role focuses on identifying and assessing ...

Cellares

Director, Quality Compliance

Bridgewater, NJ · On-site

$90K - $250K/yr

We are seeking an innovative and highly motivated Director, Quality Compliance, who will contribute significantly to the growth of the Cellares team. This individual will be responsible for leading ...

Socket.dev

Director, Quality & Compliance

Aurora, CO · On-site

$107.97 - $126.88/hr

Colorado PACE has an immediate opening for a Director of Quality & Compliance. Location: Aurora, CO Status: Full-time Schedule: Monday-Friday, 8-5 Pay Rate: $107,972 - $126,880 annually (10% bonus ...

Amgen SA

Quality Compliance, Director

Holly Springs, NC · On-site

$180 - $240/hr

QUALITY COMPLIANCE, DIRECTOR What you will do Let's do this. Let's change the world. In this vital role you will reporttotheExecutive Director of RegulatoryCompliance andprimarily provide direct ...

Amgen

Quality Compliance, Director

Holly Springs, NC · On-site

QUALITY COMPLIANCE, DIRECTOR What you will do Let's do this. Let's change the world. In this vital role you will reporttotheExecutive Director of RegulatoryCompliance andprimarily provide direct ...

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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 Aug 17, 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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What are the most commonly searched types of Quality Compliance jobs?

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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, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Director, Quality Compliance

Cellares

Bridgewater, NJ • On-site

$90K - $250K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 28 days ago

Job description

We are seeking an innovative and highly motivated Director, Quality Compliance, who will contribute significantly to the growth of the Cellares team.
This individual will be responsible for leading Quality Compliance activities for the Bridgewater site. They will be identifying and assessing regulatory and quality risks during site GMP operations ensuring adherence to global regulations and Cellares' policies and procedures. This individual will be responsible for leading the continuous inspection readiness efforts and the site's self-inspection program. They will manage routine use of the Cellares Quality Management Systems.
Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.
Responsibilities
  • Manage and lead the Quality Compliance group including quality systems, inspection management training, and operations regulatory compliance
  • Ensure the implementation and maintenance of the Cellares Quality Management System at Bridgewater with the goal of maximizing efficiency, effectiveness and compliance with all applicable GMP regulations
  • Direct the compliance programs for all cGMP areas and promote a strong Quality culture within the global organization including a strong presence in Quality, Manufacturing, MSAT, Supply Chain and Purchasing, Analytical Development, Process Development, and Engineering
  • Ensure adherence to Cellares' Quality System, regulatory standards and Federal laws
  • Support tech transfer of late stage/commercial cell therapy products and equipment coming through the organization pipeline
  • Serve as key lead during team and other technical forums with respect to compliance and regulatory strategies
  • Provide Quality direction and strategy for operational issues or technical challenges
  • Manage and oversee the Document Management System & Data Integrity programs for paper and electronic based systems ensuring compliance with 21 CFR Part 11 regulatory standards
  • Prepare and host periodic Quality Management Reviews to assess the effectiveness of the Quality Systems; identify unfavorable trends and collaborate with site stakeholders and functions to ensure their timely mitigation
  • Evaluate, contribute, and approve change controls, risk assessments, quality events, CAPAs, and other investigations as they relate to compliance and technical challenges and implementation plans
  • Contribute to CMC sections of regulatory filings, proprietary reagent filings, and other regulatory filings including client and business support paths
  • Key lead during site preparation of regulatory and customer inspections including personnel preparation and training
  • Collaborative host of regulatory and customer inspections and audits
  • Preparation and approval of follow up activities including responses, commitments, CAPAs, and other strategy plans
  • Manage and oversee the self inspection and internal audit programs
  • Perform and collaborate on global Quality audits with respect to internal and external customers
  • Responsible for the GMP Training program and ensuring its ongoing effectiveness and alignment with GMP job functions and job descriptions
  • Review and approve SOPs, manufacturing batch records, specifications, validation protocols and reports, instrument acquisitions, impact, and decommissioning, work orders, and other Quality operations as needed
  • Collaborate with functional area leads during planning and process/continuous improvement plans, projects, and gap assessments as they relate to proprietary instruments and manufacturing operations
  • Oversee and monitor Quality metrics ensuring data is understandable and translatable to the appropriate audience(s)
  • Mentor, coach, and manage staff performance and development

Requirements
  • Bachelor's degree or higher in a scientific or engineering discipline
  • 10+ years of experience in a GMP environment in pharmaceutical, biologics, vaccines, cell or gene therapy operations, including solid experience in Quality Systems and Regulatory CMC
  • 5+ years of leadership experience, and demonstrated knowledge of relevant cGMP regulations
  • Excellent knowledge of the regulations for biologics, cell and gene therapy products
  • Strong knowledge of current Good Manufacturing Practices (GMP); experience with on-site regulatory inspections is required
  • Comprehensive knowledge of global GMP and regulatory requirements for biotechnology, cell and gene therapy products and Quality by Design approaches
  • Hands-on experience with designing and implementing GMP Quality Systems
  • Ability to understand and interpret complex scientific issues across multiple projects as it relates to regulatory requirements and strategy
  • Demonstrated experience in preparing regulatory submissions and response to health authorities queries

$90,000 - $250,000 a year
Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.
This is Cellares
Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company's Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares' Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.
The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing.
Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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About Cellares

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

11 - 50 Employees

Headquarters location

South San Francisco, CA, US

Year founded

2019

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