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Director Quality Systems Jobs in Riverside, CA (NOW HIRING)

... Director of Quality. This role is responsible for maintaining and continuously improving the Quality Management System (QMS), regulatory compliance programs, supplier qualification, customer ...

Quality Manager

Ontario, CA · On-site

$140K - $180K/yr

Responsible to manage, promote, and continuously maintain a compliant quality management system by ... Exceptional leadership skills which include ability to prioritize, lead, direct, train, and ...

QC Technician

Lake Elsinore, CA · On-site

$18.25 - $23.50/hr

Perform other duties as directed by the QC Manager/Plant Manager 7.- REQUIREMENTS FOR THE POSITION ... quality systems Demonstrated ability to work independently with minimal supervision Demonstrated ...

Quality Engineer III

Irvine, CA · On-site

$76K - $99K/yr

Join a team where your contributions make a direct impact on our success. About the Role We are ... This role plays a critical part in maintaining and improving our Quality Management System ...

Quality Engineer III

Irvine, CA · On-site

$100K - $120K/yr

Join a team where your contributions make a direct impact on our success. About the Role We are ... This role plays a critical part in maintaining and improving our Quality Management System ...

Quality Engineer III

Irvine, CA · On-site

$76K - $99K/yr

Join a team where your contributions make a direct impact on our success. About the Role We are ... This role plays a critical part in maintaining and improving our Quality Management System ...

Quality Engineer III

Irvine, CA · On-site

$100K - $120K/yr

Join a team where your contributions make a direct impact on our success. About the Role We are ... This role plays a critical part in maintaining and improving our Quality Management System ...

Lead, coach, train, and develop direct reports; manage performance, timecards, evaluations ... Maintain and improve Quality Management System processes related to inspection and repair ...

Lead, coach, train, and develop direct reports; manage performance, timecards, evaluations ... Maintain and improve Quality Management System processes related to inspection and repair ...

... systems. * Perform stock purges on nonconforming product as identified and directed by the customer ... Maintain quality performance data supporting QA metrics tracking and performance improvement.

Oversees direct reports and provides guidance and leadership to the quality team in order to improve the QMS system and obtain plant and corporate objectives.Manage, lead, and facilitate root cause ...

Oversees direct reports and provides guidance and leadership to the quality team in order to improve the QMS system and obtain plant and corporate objectives.Manage, lead, and facilitate root cause ...

Perform internal audits on processes and procedures, as per direction from Quality Systems Engineer ... Direct experience conducting First Article Inspection and Report for internal manufacturing * ASQ ...

Quality Engineer, Maritime

Santa Ana, CA

$74K - $96K/yr

Develop, implement, and sustain a robust Quality Management System (QMS) that is compliant with ... Direct, hands-on experience with NavSea standards and requirements (e.g., SUBSAFE, NAVSEA S9074-AQ ...

Anduril's family of systems is powered by Lattice OS, an AI-powered operating system that turns ... Direct experience conducting First Article Inspection and Report for internal manufacturing * ASQ ...

Showing results 41-60

Director Quality Systems information

See Riverside, CA salary details

$32.3K

$131K

$222.7K

How much do director quality systems jobs pay per year?

As of Aug 21, 2026, the average yearly pay for director quality systems in Riverside, CA is $131,035.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,900.00 and $157,500.00 per year, depending on experience, location, and employer.

What is a director quality systems?

A Director of Quality Systems is a senior management professional responsible for overseeing the development, implementation, and maintenance of an organization's quality management systems. They ensure that products and processes comply with industry standards, regulatory requirements, and company policies. This role often involves leading teams, developing quality strategies, conducting audits, and driving continuous improvement initiatives across the organization. Directors of Quality Systems play a critical part in safeguarding product quality, customer satisfaction, and regulatory compliance.

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

To thrive as a Director of Quality Systems, you need deep expertise in quality management principles, regulatory compliance, process improvement, and typically a relevant degree such as in engineering or life sciences. Familiarity with quality management systems (QMS) like ISO 9001, FDA regulations, and proficiency with tools such as CAPA, risk management software, and internal audit systems is essential. Strong leadership, strategic thinking, and effective communication distinguish top performers in this role. These skills ensure the organization maintains high quality standards, meets regulatory requirements, and drives continuous improvement across all operations.

What are some common challenges faced by a director quality systems when implementing new compliance standards across an organization?

A Director of Quality Systems often encounters challenges such as resistance to change from staff, alignment of existing processes with new regulatory requirements, and ensuring consistent training across departments. Effective communication and cross-functional collaboration are key to overcoming these hurdles. The role typically involves working closely with leadership, operations, and regulatory teams to ensure that new standards are understood and integrated smoothly, minimizing disruptions while maintaining compliance.

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

AspectDirector Quality SystemsQuality Manager
ResponsibilitiesOversees quality systems, compliance, and strategic quality initiatives across departmentsManages daily quality operations, audits, and team supervision
CertificationsISO 9001 Lead Auditor, CQE, Six SigmaISO 9001 Lead Auditor, CQE, Six Sigma
Work EnvironmentStrategic planning, cross-departmental collaborationOperational focus, team management
Industry UsageCommon in regulated industries like pharmaceuticals, medical devicesWidely used in manufacturing, production facilities

The main difference between a Director Quality Systems and a Quality Manager lies in scope and strategic focus. The Director typically oversees the entire quality system, ensuring compliance and strategic alignment, while the Quality Manager handles daily quality operations and team supervision. Both roles often require similar certifications and work in regulated industries, but the Director's role is more strategic and cross-departmental.

What are the most commonly searched types of Quality Systems jobs in Riverside, CA?

The most popular types of Quality Systems jobs in Riverside, CA are:

What are popular job titles related to Director Quality Systems jobs in Riverside, CA?

For Director Quality Systems jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Director Quality Systems jobs in Riverside, CA look for?

The top searched job categories for Director Quality Systems jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Director Quality Systems jobs?

Cities near Riverside, CA with the most Director Quality Systems job openings:

Infographic showing various Director Quality Systems job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $131,035 per year, or $63 per hour.

Quality Assurance & Regulatory Manager

Nura

Irvine, CA • On-site

$100K/yr

Full-time

Posted 19 days ago


Job description

The Quality Assurance & Regulatory Manager provides leadership and day-to-day management of NURA's Quality
Assurance and Regulatory functions while supporting the strategic direction established by the Director of Quality. This role is responsible for maintaining and continuously improving the Quality Management System (QMS), regulatory compliance programs, supplier qualification, customer technical support, documentation systems, and ingredient safety initiatives.
The position leads the Quality Assurance and Regulatory team while partnering closely with Quality Control, Operations,
Procurement, Sales, Customer Service, and the China Office to ensure products consistently meet regulatory requirements, customer expectations, and NURA's quality standards.
Reporting directly to the Director of Quality, this position translates strategic initiatives into day-to-day execution, develops departmental talent, drives continuous improvement, and serves as the primary leader for Quality Assurance and Regulatory activities.
Direct Reports:
• Quality Assurance & Regulatory Staff (US)
• Documentation and Quality Assurance Specialist Staff (China)
Primary Responsibilities:
Quality Management Leadership
• Lead the Quality Assurance, Documentation, and Regulatory departments in both the US and China Offices,
establishing priorities, workload, and performance expectations.
• Manage and continuously improve NURA's Quality Management System (QMS). NURA's QMS includes but is not
limited to (NURA & Manufacturer Certification Maintenance, Ingredient and Supplier Quality Documentation,
Complaint Handling & Resolution, Ingredient/Manufacturer/Facility regulatory documentation., etc.)
• Establish departmental KPIs and monitor performance against quality objectives.
• Lead management review activities and quality performance reporting.
• Drive continuous improvement initiatives using data and risk-based decision making.
• Standardize quality processes across U.S. and China operations.
• Ensure quality and regulatory activities are executed proactively, with clear ownership, timely communication, and
defined completion timelines.
Regulatory & Compliance
• Ensure compliance with FDA, FSMA, FSVP, USDA Organic, Non-GMO Project, Kosher, Halal, SQF, customer-specific
requirements, and other applicable regulations.
• Oversee regulatory documentation, technical documentation, and customer compliance requests.
• Review regulatory changes and implement appropriate internal actions.
• Lead regulatory assessments for new products and suppliers.
• Serve as the primary internal resource for regulatory interpretation and customer regulatory inquiries.
Supplier Quality Management
• Oversee the FSVP Program at NURA ensuring qualification activities are being maintained, documentation and
assessments are being performed according to established SOPs, and compliance gaps are addressed immediately.
• Approve supplier qualification activities.
• Review supplier audits, risk assessments, CAPAs, and performance metrics.
• Drive supplier quality improvement initiatives.
• Escalate supplier quality concerns and monitor corrective actions.
Customer Quality Support
• Oversee customer questionnaires, technical documentation, specifications, COAs, allergen statements, regulatory
forms, and certification requests, ensuring proper checks are in place and systematic improvement efforts are
implemented to ensure documentation is current, accurate, and professionally answered.
• Lead customer audits and quality meetings.
• Provide technical guidance to Sales and Customer Service.
• Lead customer complaint investigations requiring Quality Assurance involvement ensuring prompt response,
effective root cause analysis, corrective actions, and document closure.
Documentation & Quality Systems
• Ensure all controlled documents remain accurate, current, and compliant.
• Approve SOPs, work instructions, forms, and quality records.
• Lead document control, change control, and document retention programs.
• Improve document workflows and digital quality systems.
• Ensure consistency and version control across all technical documentation distributed internally and externally.
Product Safety & Risk Management
• Maintain HACCP, Food Safety Plan, Food Defense, Recall, Traceability, and Risk Assessment programs.
• Lead internal audits and regulatory inspections.
• Coordinate external certification audits.
• Ensure corrective and preventive actions are implemented effectively.
Team Leadership
• Recruit, coach, mentor, and develop Quality Assurance and Regulatory personnel.
• Conduct performance reviews and establish employee development plans.
• Foster accountability, ownership, urgency, collaboration, and continuous learning.
• Build cross-functional partnerships throughout the organization.
• Foster accountability, ownership, urgency, collaboration, professionalism and a proactive mindset.
Cross-Functional Collaboration Partner closely with:
• Quality Control
• Purchasing
• Logistics
• Warehouse Operations
• Sales
• Customer Service
• China Office
• Executive Leadership
Decision-Making Authority
• Approve supplier qualification status.
• Approve controlled quality documents.
• Approve regulatory documentation.
• Approve quality investigations and CAPAs.
• Recommend supplier disqualification when appropriate.
• Recommend product disposition for quality-related issues.
• Escalate significant business risks to the Director of Quality & Regulatory.
Key Performance Indicators:
• Audit Performances (Internal and External facilities). Successfully manage internal audits, supplier audits, customer
audits, and third-party certification audits, with timely closure of findings and corrective actions.
• Complaint Closure Turn Around Time and Customer Management. Ensure customer complaints, investigations, root
cause analysis, and corrective actions are completed accurately, communicated appropriately, and closed within
established timeline.
• Document and Technical Requests closure time. Ensure customer questionnaires, specifications, regulatory
documents, certifications, and technical requests are completed accurately, consistently, and within established
turnaround times.
• Manufacturer engagement and development. Supplier qualification completed on schedule and supplier quality
issues resolved.
Leadership:
• Team engagement
• Employee development
• Cross-functional collaboration
• Implementation of continuous improvement initiatives.
Qualifications
Education: Bachelor's degree in Food Science, Microbiology, Chemistry, Biology, Regulatory Affairs, Quality Assurance, or related discipline.
Experience
• 5+ years in Quality Assurance or Regulatory Affairs within food, dietary supplements, or ingredient
manufacturing/distribution.
• 2+ years leading Quality or Regulatory teams.
• Strong working knowledge of FDA, FSMA, FSVP, GMPs, HACCP, and supplier quality systems.
• Experience managing customer audits and regulatory inspections.
• Experience developing and improving Quality Management Systems.
• Demonstrated experience using TraceGains for supplier qualification, document management, and customer
technical documentation.
Core Competencies
• Leadership & Coaching
• Strategic Thinking
• Regulatory Expertise
• Quality Systems Management
• Supplier Qualification and Maintenance.
• Risk Assessment
• Root Cause Analysis
• CAPA Management
• Customer Management
• Project Management
• Cross-Functional Leadership
• Continuous Improvement
• Strong Communication
• Data-Driven Decision Making
• Change Management
• Execution and Accountability