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Quality Control Program Manager Jobs in Sylmar, CA

Description JOB TITLE: Sr. Manager, Quality Control LOCATION: Los Angeles, CA (Hybrid in our ... Experience designing and operating QC or compliance monitoring programs focused on credit policy ...

SUPERVISOR QUALITY CONTROL

Inglewood, CA · On-site

$28.85 - $36.35/hr

Our collaboration extends across a diverse array of programs and platforms, including major ... Quality Control Supervisor provides support to the QC manager by overseeing and working alongside ...

SUPERVISOR QUALITY CONTROL

Inglewood, CA · On-site

$28.85 - $36.35/hr

Our collaboration extends across a diverse array of programs and platforms, including major ... Quality Control Supervisor provides support to the QC manager by overseeing and working alongside ...

The role involves supporting and troubleshooting issues at seven *** QC organizations in templating, template qualification, and using the established ELN Biovia SmartLab and consumable management ...

... program support. Working knowledge of phase-appropriate quality systems, including deviations, CAPA, change control, and electronic quality management systems. Excellent interpersonal, verbal, and ...

... program support. Working knowledge of phase-appropriate quality systems, including deviations, CAPA, change control, and electronic quality management systems. Excellent interpersonal, verbal, and ...

QA / QC Supervisor

Vernon, CA · On-site

$75K - $85K/yr

Aid QA Supervisor and Technical Manager in overseeing/reviewing pre-operations inspections and Environmental Monitoring Program. * Advisor to QC/Production Technicians on quality deviations/issues

We are seeking a full-time Quality Control (QC) Technician to join our team. As a member of our ... Sick Days * 401(k) * Discount Programs * Life Insurance * Disability Insurance * Employee ...

We are seeking a full-time Quality Control (QC) Technician to join our team. As a member of our ... Sick Days * 401(k) * Discount Programs * Life Insurance * Disability Insurance * Employee ...

Support inventory management of laboratory supplies, samples, and materials * Follow SOPs, GMPs, and internal quality procedures * Assist with continuous improvement of QC and laboratory processes ...

Continue developing technical capability through the site's qualification program and support ... Manage changing priorities while maintaining accuracy, attention to detail, and timely completion ...

New

QA+QC Manager

Los Angeles, CA · On-site

$90K - $130K/yr

Through its Bigger Than Beauty™ program, every product purchased results in a donation to help ... As the QA/QC Manager, you will work closely with internal teams, contract manufacturers, and ...

QA+QC Manager

Los Angeles, CA · On-site

$90K - $130K/yr

Through its Bigger Than Beauty program, every product purchased results in a donation to help ... As the QA/QC Manager, you will work closely with internal teams, contract manufacturers, and ...

... and management teams. Key Responsibilities * Inspect aluminum window and door components before ... Previous quality control, inspection, manufacturing, anodizing, metal finishing, or window and door ...

Showing results 41-60

Quality Control Program Manager information

See Sylmar, CA salary details

$31K

$82.6K

$131.6K

How much do quality control program manager jobs pay per year?

As of Sep 5, 2026, the average yearly pay for quality control program manager in Sylmar, CA is $82,630.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,500.00 and $101,600.00 per year, depending on experience, location, and employer.

What is a quality control program manager?

Quality Control Program Managers are professionals who oversee and coordinate quality assurance activities within an organization. They develop, implement, and maintain quality control systems to ensure that products or services meet established standards and regulatory requirements. These managers lead teams, conduct audits and inspections, analyze quality data, and collaborate with other departments to resolve quality issues. Their role is critical in minimizing defects, improving processes, and ensuring customer satisfaction.

How does a quality control program manager typically collaborate with cross-functional teams to ensure product standards are met?

A Quality Control Program Manager regularly works alongside teams such as manufacturing, engineering, regulatory affairs, and supply chain to align quality standards across all stages of production. This collaboration often involves participating in cross-functional meetings, reviewing process documentation, and leading corrective action initiatives when deviations occur. By fostering open communication and implementing feedback loops, the manager ensures that quality objectives are understood and met company-wide, minimizing errors and supporting continuous improvement.

What are the key skills and qualifications needed to thrive as a quality control program manager, and why are they important?

To thrive as a Quality Control Program Manager, you need expertise in quality assurance methodologies, data analysis, and process improvement, often supported by a degree in engineering or a related field. Familiarity with quality management systems (such as ISO 9001), Six Sigma certification, and proficiency in statistical software are typically required. Strong leadership, problem-solving abilities, and effective communication skills help you lead teams and drive compliance. These competencies are crucial to ensure product quality, regulatory adherence, and continuous organizational improvement.

What is the difference between Quality Control Program Manager vs Quality Assurance Specialist?

AspectQuality Control Program ManagerQuality Assurance Specialist
CertificationsISO 9001 Lead Auditor, Six SigmaISO 9001 Internal Auditor, Six Sigma Green Belt
Work EnvironmentOversees quality control processes across projects, often in manufacturing or production settingsFocuses on developing and implementing quality assurance procedures, typically in labs or office settings
Employer & Industry UsageManufacturing, aerospace, automotive, constructionPharmaceuticals, software, manufacturing, healthcare

The Quality Control Program Manager primarily manages and oversees quality control processes to ensure products meet standards, while the Quality Assurance Specialist develops and maintains quality assurance systems to prevent defects. Both roles require similar certifications and work in related environments, but their focus differs: control vs. assurance.

What cities near Sylmar, CA are hiring for Quality Control Program Manager jobs?

Cities near Sylmar, CA with the most Quality Control Program Manager job openings:

cGMP Quality Control (QC) Specialist

USC Gould School of Law

Los Angeles, CA • On-site

$87K - $92K/yr

Full-time

Re-posted yesterday


Key responsibilities

  • Performs cGMP batch release testing to ensure the quality of pharmaceuticals and biopharmaceuticals before patient application.

  • Operates instrumentation needed for cell and gene therapy manufacturing and assists in technology transfer of manufacturing processes.

  • Supervises and directs junior staff, provides verification of facility operations and equipment, and supports compliance with cGMP guidelines.


Job description

The University of Southern California (USC), founded in 1880, is located in the heart of downtown L.A. and is the largest private employer in the City of Los Angeles. As an employee of USC, you will be a part of a world-class research university and a member of the "Trojan Family," which is comprised of the faculty, students and staff that make the university what it is.

USC's Keck School of Medicine, Department of Medicine is seeking a dynamic individual to work on the manufacturing of biologics and drugs for cell and gene therapy of internal/external users in the university's current Good Manufacturing Practices (cGMP) facility. The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and implementing quality control testing, assays, and procedures for materials and final cell therapy products manufacturing. The position will also be responsible for ensuring consistency with current Good Manufacturing Practice (cGMP) principles.

Job Accountabilities:

  • Supports cGMP manufacturing operations with responsibility for quality control. Performs cGMP batch release testing to ensure pharmaceuticals and biopharmaceuticals are of the highest possible quality before being applied to patients. Writes and reviews qualifications (e.g., installation, operation, performance), facility operation plans and reports, standard operating procedures, and batch records as required. Completes batch record documentation, all appropriate equipment log entries, and cGMP documentation.
  • Operates instrumentation needed for cell and gene therapy manufacturing (e.g., cell counters, bioreactors, centrifuges, biological safety cabinets). Assists in technology transfer of manufacturing processes from pre-clinical into cGMP environment.
  • Provides verification of facility operations and equipment, along with advanced problem-solving, troubleshooting, and consultation support, as needed. Supervises and directs junior staff to achieve project goals. Serves as a resource to cGMP facility management in identifying and assessing the appropriate complement of resources and support needed to successfully implement and execute projects.
  • Maintains confidentiality for patient identification, specimen labeling, and specimen verification during batch testing. Performs duties in a clean room environment, when needed and while fully gowned (e.g., mask, coverall, gloves), following cGMP guidelines and using aseptic techniques. Works with senior staff to ensure facilities' compliance with all applicable regulations.
  • Attends routine meetings with the management team for progress reports on projects, facility needs, and discussion of any other required items. Improves current methods and evaluates innovative techniques in quality control testing for cell therapy and biologics.
  • Promotes an environment that fosters inclusive relationships and creates unbiased opportunities for contributions through ideas, words, and actions that uphold principles of the USC Code of Ethics.
  • Performs other related duties as assigned or requested. The university reserves the right to add or change duties at any time.

Successful Candidates Must Demonstrate:

  • Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of all aspects of biotechnology and cell therapy. Demonstrated passion for solving complex scientific issues. Experience with Food and Drug Administration regulations and clinical trials. Extensive leadership experience.

Salary Range:

The annual base salary range for this position is $87,576.76 - $92,000. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state, and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.

*This is a 3-year fixed-term position.

USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to the Background Screening Policy Appendix D for specific employment screen implications for the position for which you are applying.

Minimum Education: Bachelor's degree
Minimum Experience: 3 years
Supervises: May lead one or more employees performing similar work
Minimum Field of Expertise: Bachelor's degree in a scientific discipline (e.g., pharmaceutical, biologics). Three years' experience in cellular or biological manufacturing with quality control responsibilities. Demonstrated knowledge base with Good Manufacturing Practices (e.g., cGMPs, GLPs, GDPs). Experience with standard operating procedures in a cGMP laboratory setting. Demonstrated ability to work as an individual contributor and in a dynamic team environment. Excellent written and oral communication skills.
Preferred Education: Master's Degree
Preferred Experience: 5 Years
Preferred Field of Expertise: Biotechnology and life sciences

USC is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other characteristic protected by law or USC policy. USC observes affirmative action obligations consistent with state and federal law. USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to theBackground Screening Policy Appendix Dfor specific employment screen implications for the position for which you are applying.

We provide reasonable accommodations to applicants and employees with disabilities. Applicants with questions about access or requiring a reasonable accommodation for any part of the application or hiring process should contact USC Human Resources by phone at (213) 821-8100, or by email atuschr@usc.edu. Inquiries will be treated as confidential to the extent permitted by law.

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If you are a current USC employee, please apply to this  USC job posting in Workday by copying and pasting this link into your browser:

https://wd5.myworkday.com/usc/d/inst/1$9925/9925$125114.htmld