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Qa Supervisor Jobs in Riverside, CA (NOW HIRING)

Quality Assurance Auditor

Ontario, CA · On-site

$32.03 - $40.19/hr

Calibrate audit requirements and training for operations managers/supervisors to comply with all critical customers' requirements, and to ensure HQ QA policy compliance. Maintain audit documents for ...

Calibrate audit requirements and training for operations managers/supervisors to comply with all critical customers' requirements, and to ensure HQ QA policy compliance. Maintain audit documents for ...

QA Technician

Rialto, CA · On-site

$20.25 - $22.50/hr

Document abnormal production conditions and communicate immediately with the Production Supervisor and QA Manager. * Prepare and maintain required documentation of test results. * Calibrate all ...

Follow work instructions as set out by the QA Supervisor and EQS-Quality Manager. * Verify incoming, in-process, and outgoing product with customer requirements. * Validate parts and materials to ...

Quality Assurance Specialist Location: Pomona, California Duration: 12 Months 100% Onsite Summary ... of the Supervisor/Manager. Key Responsibilities * Perform batch record review, record ...

Quality Assurance Specialist Location: Ontario, CA Type: Direct Hire Compensation: $70,000 Work Model: Onsite Hours: 40.0 Responsibilities * Ensure compliance with FDA regulations, GMP requirements ...

New

Manager, Quality Assurance

Ontario, CA · On-site

$11K - $141K/mo

Monitor the performance and competencies of plant QA staff and provide leadership, coaching and development as needed * Lead the execution of cultural changes and activities needed to support Primo ...

New

Quality Assurance Specialist

Irvine, CA · On-site

$28.50 - $33/hr

We are looking for a Quality Assurance Specialist to support leave administration for employees in Irvine, California. This Long-term Contract position will oversee end-to-end leave cases, coordinate ...

QA Auditor

Tustin, CA · Hybrid

$103K - $129K/yr

Serves as the QA subject matter expert in the creation and revision of Raw Material Specifications ... Days and hours of work are Monday through Friday unless otherwise stated by Supervisor. The ...

Job Overview The Manager of Quality Assurance will oversee the activity of the QA department and team, developing, implementing, and maintaining a system of quality and reliability testing for the ...

QA Auditor

Tustin, CA · On-site

$103.20 - $129/hr

Serves as the QA subject matter expert in the creation and revision of Raw Material Specifications ... Days and hours of work are Monday through Friday unless otherwise stated by Supervisor. The ...

Showing results 41-60

Qa Supervisor information

See Riverside, CA salary details

$39.6K

$123.2K

$186.7K

How much do qa supervisor jobs pay per year?

As of Aug 22, 2026, the average yearly pay for qa supervisor in Riverside, CA is $123,182.00, according to ZipRecruiter salary data. Most workers in this role earn between $86,600.00 and $150,800.00 per year, depending on experience, location, and employer.

What is a QA supervisor?

QA Supervisors, or Quality Assurance Supervisors, are professionals responsible for overseeing the quality assurance processes within a company. They ensure that products or services meet established standards of quality, reliability, and performance before reaching customers. QA Supervisors manage teams of QA technicians or inspectors, develop testing procedures, monitor compliance, and report on quality metrics. Their role is crucial in industries like manufacturing, pharmaceuticals, and food production, where product quality and safety are paramount.

What skills and qualifications are needed to be a QA supervisor?

To thrive as a QA Supervisor, you need a solid background in quality assurance processes, attention to detail, and typically a degree in a related field such as engineering or life sciences. Familiarity with quality management systems (QMS), ISO standards, auditing tools, and relevant certifications like Six Sigma or ASQ are highly valuable. Strong leadership, problem-solving abilities, and effective communication set outstanding QA Supervisors apart. These skills ensure product quality, regulatory compliance, and efficient team performance within a quality-driven environment.

How does a QA supervisor collaborate with other departments to ensure product quality?

QA Supervisors play a key role in cross-functional collaboration, regularly working with production, engineering, and supply chain teams to uphold quality standards. They facilitate communication between departments, ensuring that any quality issues are promptly identified and addressed. By leading root cause analyses and participating in regular meetings, QA Supervisors help align quality objectives across the organization. This collaborative approach not only prevents defects but also fosters a culture of continuous improvement.

What are popular job titles related to Qa Supervisor jobs in Riverside, CA?

For Qa Supervisor jobs in Riverside, CA, the most frequently searched job titles are:

What cities near Riverside, CA are hiring for Qa Supervisor jobs?

Cities near Riverside, CA with the most Qa Supervisor job openings:

Infographic showing various Qa Supervisor job openings in Riverside, CA as of August 2026, with employment types broken down into 87% Full Time, and 13% Contract. Highlights an 100% In-person job distribution, with an average salary of $123,182 per year, or $59.2 per hour.

Quality Assurance Specialist III

BioPhase Solutions

Anaheim, CA • On-site

$35 - $40/hr

Full-time

Re-posted 7 days ago


Job description

BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Quality Assurance Specialist III to work for a leading Greater Orange County area contract manufacturing company.

Pay Rate: $35-40/hour
Duration: 6+ months - possibility of conversion down the line, but not guaranteed

Responsibilities:
  • QC testing pH, water content, assay titration, Loss on drying. UV. FTIR, HPLC, GC., mineral and microbiology The candidate also familiar with USP. EP. JP compendial testing.
  • US FDA 21CFR210, 211, 11 and applicable ICH guidance documents. Develop and revise QA procedures to strengthen cGMP compliance.
  • Reviewing test results and supporting technical documentation. Work directly with operations management to resolve findings noted during the review process.
  • Performing release of raw materials and consumables.
  • Reviewing and approving Certificate of Analysis for raw materials, drug substance and drug products.
  • Collaborating effectively with operations management to review and approve: SOPs, protocols, reports, equipment qualifications and calibrations, change controls, specifications trend reports and other quality documentation.
  • Responsible for writing/revising Quality Assurance procedures to strengthen compliance with cGMPs.
  • Reviewing and approving deviations and gather/issue quality metrics reports to QA management.
  • Providing QA support during cGMP compliance inspections of the facility by clients, the FDA and/or other regulatory bodies.
  • Acting as a co-auditor during supplier/internal quality audits
  • Providing subject matter expertise for the supplier assurance program at the site
  • Providing QA management with the support needed for compliance training.
  • Maintaining workspace cleanliness by adhering to the 5S method of organization.
  • Abiding by safe work practices and adhere to general safety rules, performing all duties in a safe manner and never placing yourself or those around you in an unsafe condition. Report all unsafe conditions to your supervisor.
  • This list of duties and responsibilities is not all inclusive and may be expanded to include other duties and responsibilities, as management may deem necessary.
Experience/Requirements:
  • Bachelor's degree with 3-5+ years in Lab & QA, or a minimum of 4+ years with both lab & QA related work experience.
  • Advance experience and knowledge of cGMP regulations, and FDA and ICH guidelines as they pertain to contract laboratory and/or aseptic manufacturing operations.
  • Advance experience and knowledge of USP, Pharm. Eur. (EudraLex) and other applicable standards.
  • Advance knowledge of root cause investigation and problem solving; experience in the use of 5 Whys and/or other appropriate root cause investigation tools.
  • Advance experience and knowledge in the use of LIMS and electronic documentation systems.
  • Strong interpersonal skills. Must be able to express oral and written communication in a clear and concise manner and effectively present information and respond to questions from managers, customers and employees.
  • Effective organizational and time management skills with the ability to multi-task and prioritize assignments as needed.
  • Works on complex issues; exercises good judgement in selecting methods, techniques and evaluation criteria for obtaining results while handling Quality Assurance tasks.
  • Ability to perform routine work with minimal instructions, determines methods and procedures on new assignments.
  • May coordinate activities of other personnel.
  • Ability to work effectively under pressure in a rapidly changing environment.
  • Ability to work well independently and effectively with a wide variety of colleagues both inter- and intra- departmentally.
  • Ability to seek critical information from key resources to assist in problem solving.
  • Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Project, etc.).
Please send resumes to tiffany@biophaseinc.com and visit our website at www.biophaseinc.com for additional job opportunities!!!