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

LGM Pharma, LLC

DIRECTOR OF QUALITY

Irvine, CA · On-site

$135K - $160K/yr

We have an open position for a Director of Quality located in Irvine, California facility to ... Oversight of Quality Systems at the facility ensuring all products produced consistently meet ...

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:

New

NEOGEN CARE

Director of Quality

Ontario, CA · On-site

The Director of Quality utilizes their expertise in quality management principles and regulatory standards daily to design and refine quality systems that ensure compliance and operational efficiency.

Lubrizol Corporation

Senior Quality Manager

Corona, CA · Hybrid

Drive development, implementation, and improvement in our Operation Quality Systems. * Manage the Quality Engineering team and direct the activities of Quality Engineers, Quality Control Supervisor ...

Lubrizol Corporation

Senior Quality Manager

Corona, CA · Hybrid

Drive development, implementation, and improvement in our Operation Quality Systems. * Manage the Quality Engineering team and direct the activities of Quality Engineers, Quality Control Supervisor ...

Lubrizol Corporation

Senior Quality Manager

Corona, CA · On-site

Drive development, implementation, and improvement in our Operation Quality Systems. * Manage the Quality Engineering team and direct the activities of Quality Engineers, Quality Control Supervisor ...

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 ...

Kirkhill

Quality Inspector - Scanner

Brea, CA

Maintains relevant updated specification, standard and quality systems documents. * Performs ... Integrity and Trust - Widely trusted and seen as direct and truthful. * Functional/Technical Skills ...

Kirkhill Inc.

Quality Inspector - Scanner

Brea, CA · On-site

$30 - $38/hr

Maintains relevant updated specification, standard and quality systems documents. * Performs ... Integrity and Trust - Widely trusted and seen as direct and truthful. * Functional/Technical Skills ...

Kirkhill Inc.

Quality Inspector - Scanner

Brea, CA

Maintains relevant updated specification, standard and quality systems documents. * Performs ... Integrity and Trust - Widely trusted and seen as direct and truthful. * Functional/Technical Skills ...

Kirkhill Inc.

Quality Inspector - Scanner

Brea, CA · On-site

$30 - $38/hr

Maintains relevant updated specification, standard and quality systems documents. * Performs ... Integrity and Trust - Widely trusted and seen as direct and truthful. * Functional/Technical Skills ...

Balda C Brewer

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 ...

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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 Jun 15, 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.

How much does a QA director make in the US?

A Quality Assurance (QA) Director typically earns between $120,000 and $180,000 annually in the US, depending on experience, industry, and location. Compensation may also include bonuses and benefits, and the role often requires strong leadership, quality management skills, and familiarity with regulatory standards.

What jobs pay $500,000 a year in the US?

In the US, high-level executive roles such as CEOs, CFOs, and other C-suite executives often earn $500,000 or more annually. Certain specialized professions like top surgeons, successful entrepreneurs, and highly experienced professionals in finance or technology may also reach or exceed this compensation level, especially with bonuses, stock options, or profit sharing. For a Director of Quality Systems, reaching this salary typically requires extensive experience, leadership responsibilities, and often working in large corporations or industries with high profit margins.

What are the key skills and qualifications needed to thrive as a Director of Quality Systems, and why are they important?

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 does a director of quality systems do?

A director of quality systems oversees the development, implementation, and maintenance of quality management systems within an organization. They ensure compliance with industry standards, lead quality audits, and collaborate with cross-functional teams to improve product or service quality, often utilizing tools like ISO standards and quality metrics. This role typically requires strong leadership, regulatory knowledge, and experience in quality assurance processes.

What are some common challenges faced by a Director of 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 are 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.

Is QC a high paying job?

Quality Control (QC) roles can offer competitive salaries, especially in industries like manufacturing, pharmaceuticals, and technology. Salaries for QC positions vary based on experience, location, and industry, with senior roles or those requiring specialized skills often paying higher wages.
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 June 2026, with employment types broken down into 5% As Needed, 60% Full Time, 25% Part Time, and 10% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $131,035 per year, or $63 per hour.
DIRECTOR OF QUALITY

DIRECTOR OF QUALITY

LGM Pharma, LLC

Irvine, CA • On-site

$135K - $160K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 23 days ago

Job description


We have an open position for a Director of Quality located in Irvine, California facility to oversee the Quality Department for MainPointe Pharmaceuticals, LLC.


RESPONSIBILITIES:


  • Oversight of Quality Systems at the facility ensuring all products produced consistently meet quality specifications.
  • Plans and directs resources and activities of the Quality Assurance functions and assures that facility-wide activities are performed and maintained in compliance with the appropriate standards and regulations.
  • Manages systems for raw materials, product and document review, approval, or rejections.
  • Oversight of Quality Control laboratory
  • Ensure that cGMP requirements and quality standards are recognized, understood and maintained across the facility.
  • Assures facility and equipment systems meet cGMP requirements.
  • Oversee investigations of all non-conformances (deviations, OOS) and chair’s site Material Review Boards.
  • Establishment of raw material and finished product specifications based on regulatory requirements and customer needs and in conjunction with product development and other site quality departments.
  • Author and/or approve standard operating procedures, protocols, qualifications, and quality reports.
  • Manages customer complaint and AER systems and associated investigations, resolution and CAPA’s.
  • Assure all employees are trained in cGMP.
  • Actively participate in production, quality unit, and management meetings as needed.
  • Development and maintenance of appropriate tracking methods for quality process improvements.
  • Coordinate and manage vendor audits.
  • Manage Annual Product Review (APR) program and assure Product Quality Reports are completed on a timely basis.
  • Manages the Quality Key Performance Indicator data collection and reporting in support of Management Review.
  • Work across all disciplines (e.g. manufacturing, clinical, R&D, etc.) to ensure that the facility maintains a state of readiness for inspection by regulatory agencies.
  • Serves as an interface for inspections by FDA, DEA, and other regulatory agencies and customers.
  • Support oversight of document control systems.
  • Use of statistical process control to evaluate trends.
  • Development and maintenance of appropriate quality agreements with customers.
  • Budgetary and managerial responsibility for Quality Assurance and Quality Control departments at facility.



QUALIFICATIONS:

  • Bachelor’s degree in scientific discipline
  • 12+ years’ related experience in a Pharmaceutical GMP regulated manufacturing environment, with a demonstrated history of progressive growth and advancement required
  • 5+ years of management experience; or equivalent combination of education and experience
  • Strong commitment to quality standards with leadership and management skills.
  • Ability to read and interpret technical procedures, SOP’s, GMP’s and governmental regulations.
  • Strong communication skills, both written and verbal.
  • Possess positive qualities of effective leadership, staff motivation and conflict resolution.
  • Strong attention to detail and ability to multitask.
  • ASQC quality certifications, ISO 9000 or other Audit training preferred.


At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.