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

Kelly Services

Director of Quality

Claremont, CA · On-site

Direct Hire** **$170-$185K/year** Job Type: Full-time Location: Onsite in Claremont, CA Job ... Work collaboratively to implement phase appropriate requirements and optimize Quality systems for ...

Divergent

Director, Supplier Quality

Irvine, CA

You will build and scale supplier quality systems appropriate for a high-growth, advanced ... M08/ Director, Supplier Quality: $193,100 - $236,020 Pay Range $193,100--$236,020 USD What We Offer:

Revelyst

Director, Supplier Quality

Irvine, CA · On-site

$200 - $220/hr

Director of Supplier Quality We are seeking an experienced Director of Supplier Quality to join the ... Global Quality Systems & Metrics: Standardize quality processes, documentation, and KPIs across all ...

New

Revelyst

Director, Supplier Quality

Irvine, CA · On-site

We are seeking an experienced Director of Supplier Quality to join the Global Operations team and ... Global Quality Systems & Metrics: Standardize quality processes, documentation, and KPIs across all ...

New

Revelyst

Director, Supplier Quality

Irvine, CA

We are seeking an experienced Director of Supplier Quality to join the Global Operations team and ... Global Quality Systems & Metrics: Standardize quality processes, documentation, and KPIs across all ...

New

Diality

Director, Regulatory Affairs

Irvine, CA · On-site

$205K - $230K/yr

This position is also responsible for supporting the Quality Management System and will serve as the Regulatory Affairs lead on product teams. The Regulatory Affairs Director will also act as the ...

Diality Inc

Director, Regulatory Affairs

Irvine, CA · On-site

$205K - $230K/yr

This position is also responsible for supporting the Quality Management System and will serve as the Regulatory Affairs lead on product teams. The Regulatory Affairs Director will also act as the ...

Nura

Quality Assurance & Regulatory Manager

Irvine, CA · On-site

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

New

Alcon

Director, R&D Quality Assurance

Lake Forest, CA · On-site

As Director, R&D Quality Assurance, you will play a critical leadership role in advancing quality ... You will guide the implementation of quality systems for new products, post-market improvements ...

Nura

Quality Assurance & Regulatory Manager

Irvine, CA · On-site

... the Director of Quality. This roleis responsible for maintaining and continuously improving the Quality Management System (QMS), regulatory complianceprograms, supplier qualification, customer ...

New

Nura

Quality Assurance & Regulatory Manager

Irvine, CA · On-site

... the Director of Quality. This roleis responsible for maintaining and continuously improving the Quality Management System (QMS), regulatory complianceprograms, supplier qualification, customer ...

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Showing results 21-40

All JobsQuality Systems JobsDirector Quality Systems JobsDirector Quality Systems Jobs in Riverside, CA

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 7, 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 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 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 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 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:
Director Quality Systems jobs near you
Infographic showing various Director Quality Systems job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $131,035 per year, or $63 per hour.

Director of Quality

Kelly Services

Claremont, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 9 days ago

Job description

Director of Quality
**Direct Hire**
**$170-$185K/year**
Job Type:
Full-time
Location:
Onsite in Claremont, CA
Job Overview:
Our customer is seeking a talented Director of Quality to lead our Quality Assurance and Quality Control groups and advance the strategy to achieve goals for GMP readiness. The position requires expertise in analytical method development and testing, CMC regulatory requirements, GMP compliance and eQMS systems. The Quality Director is responsible for overall management of Quality operations and partnership with manufacturing and project management functions to build a strong quality culture with an emphasis on teamwork, knowledge sharing and continuous improvement.
Roles & Responsibilities:
  • Defines and implements the strategic and operational plan for Quality, in alignment with the corporate goals and priorities to strengthen GMP readiness
  • Work collaboratively to implement phase appropriate requirements and optimize Quality systems for our customer’s pre-clinical and clinical programs
  • Ensures procedures, specifications, quality reports, and other quality documents are up-to-date, and support the transition to eQMS.
  • Effectively manage and mentor quality personnel to achieve goals, resource planning and adhere to company policies
  • Participate or lead appropriate meetings with QA, QC and manufacturing teams to ensure alignment of efforts and priorities.
  • Act as a subject matter expert on quality issues and compliance-related matters for manufacturing, packaging and distribution to CRO’s.
  • Work collaboratively with Manufacturing operations to ensure adequate procedures and ensure sufficient QA resources for on-the-floor oversight, line clearance and other QA functions in Production area.
  • Oversee QA review and approval of Master Batch Records, Test Methods, forms, procedures, test methods and other master documents related to Production & QC.
  • Manage and ensure that deviations, discrepancies, change controls, etc. related to Production & QC are resolved and closed prior to batch release.
  • Manage data integrity practices/ requirements in Production & QC as established by our customer's Policies, site procedures and regulations.
  • Oversee timely initiation of deviations and investigations related to Production & QC; assure investigations are completed in satisfactory manner and in accordance with the level/ classification of discrepancy.
  • Lead initiation, evaluation and completion of Change Controls related to Production & QC.
  • Ensure timely implementation of Corrective and Preventive Actions for continuous improvement of system and activities in Production & QC
  • Provide Quality support and assistance for facilities, utilities, and equipment; review and disposition Out-of-Tolerance records for equipment; review technical, investigation, validation/ qualification documentation related to Production & QC with appropriate audit trail.
  • Set up trending for QC analytics and provide annual reports to management.
  • Conduct internal & external audits in order to verify that regulatory and quality requirements have been met.
  • Support Management during government or regulatory agency inspections and audits.
  • Oversee Quality audits for incoming materials and CRO’s, and vendor qualification strategy.
Qualifications & Education Requirements:
  • BS/MS in the life sciences or a technical discipline; advanced degree in Chemistry, Biology, or equivalent preferred.
  • 5+ years of experience in Quality in the pharma or biotech industry with demonstrated experience in personnel supervision and/or management.
  • Understanding of Quality system requirements including deviations, OOS, CAPAs, and eQMS implementation
  • Comprehensive understanding of CFR regulations (21CFR Part 210, 211 etc.), ICH guidelines, quality management systems initiatives, and standards.
  • Working knowledge and ability to apply GMPs in conformance to U.S. standards and exposure to CMC/Pharma Development and development teams.
  • Knowledge of drug development lifecycle comprehensive understanding of regulations and guidelines and ability to apply to enhance probability of regulatory success and regulatory compliance.
  • Experience performing GMP audits of manufacturing facilities of vendors and internal operations.
  • Understanding of computer systems validation methodologies and related industry expectations.
Required Personal Skills:
  • Enthusiasm to help build the assets of a small, growing pharmaceutical company.
  • Comfortable in a fast-paced, small company environment with minimal direction and able to adjust workload based upon changing priorities.
  • Proficient in MS Word, Excel, Power Point and other applications. Familiarity with electronic systems for Batch Record, Quality Management Systems, is a plus.
  • Excellent teamwork and collaboration skills to ensure alignment across teams.
  • Excellent team building, leadership, and management skills.
  • Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment.
  • Strong problem solving/process improvement skills with ability to both be a part of and own solutions.
  • Adept at applying risk-based and phase-appropriate quality approaches.
  • Strong attention to detail and the ability to independently prioritize and multitask.
Employment Eligibility Requirements:
  • All applicants must provide proof of authorization to work in the United States for US government contracts (FARS 52.222-54)
  • All applicants must pass a background check and E-Verify employment eligibility verification prior to start date
Applicants should provide a resume, and cover letter. Applications without a cover letter will not be considered. Three references will be required for candidates prior to final job offer.
*This position is full-time at the facility in Claremont, CA and is not eligible for remote work.
Our customer is an equal opportunity employer. All qualified applicants will receive consideration for employment and advancement without regard to sex, race, color, age, national origin, religion, disability, genetic information, marital status, sexual orientation, gender identity/reassignment, citizenship, pregnancy or maternity, veteran status, or any other status protected by applicable national, federal, state or local law.
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Government Solutions?

Looking to connect with premier government agencies or the top 25 federal government contractors? Kelly Government Solutions partners with these organizations to create expert talent solutions that solve the world’s most critical challenges. We offer a variety of full-time, project (SOW), seasonal, and surge support opportunities in science, engineering, technology, professional, and administrative support roles. Our experts will connect you to the opportunity that fits your schedule and interests and handle the details of transferring and processing all levels of security clearances. It’s just another way we make the job search work for you.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
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