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Quality System Associate Jobs in California (NOW HIRING)

Unigen

Quality System Specialist

Newark, CA · On-site

$78K - $88K/yr

Quality System Specialist Job Function: Quality Department Report to: Senior Quality Assurance ... Associate's degree in related field. * 2+ years of experience in management systems related to ...

GRIFOLS, S.A.

Quality Systems Associate

Van Nuys, CA · On-site

Quality Systems Associate Summary: Under the direct supervision of the Quality Systems Manager, perform quality assurance and Training functions to ensure compliance with internal and external ...

Jobtailor

Quality Systems Associate

Los Angeles, CA · On-site

Under the direct supervision of the Quality Systems Manager, perform quality assurance and training functions to ensure compliance with internal and external regulations and protocol. * Completes ...

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Quality System Associate information

What is the difference between Quality System Associate vs Quality Control Technician?

AspectQuality System AssociateQuality Control Technician
CertificationsISO 9001, GMP, internal auditsISO 9001, GMP, laboratory testing certifications
Work EnvironmentDocumentation, audits, compliance activitiesLaboratory testing, product inspection
Employer & Industry UsageManufacturing, pharmaceuticals, medical devicesPharmaceuticals, food production, manufacturing

The Quality System Associate focuses on maintaining quality management systems, documentation, and compliance processes. In contrast, the Quality Control Technician primarily conducts product testing and inspections to ensure quality standards. Both roles are essential in manufacturing and regulated industries, but they differ in daily tasks and focus areas.

What are the most commonly searched types of Quality System jobs in California?

The most popular types of Quality System jobs in California are:

What cities in California are hiring for Quality System Associate jobs?

Cities in California with the most Quality System Associate job openings:

Quality System Specialist

Newark, CA • On-site

Unigen
See more jobs at Unigenexternal

$78K - $88K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 16 days ago

Key responsibilities

  • Develop, implement, and maintain management systems such as QMS, EMS, OHSMS, and ISMS in accordance with relevant standards and requirements.

  • Coordinate internal and external audits, track nonconformities, and manage certification and recertification processes.

  • Collaborate with departments to establish quality objectives, monitor progress, and support continuous improvement initiatives.

Job description

About Unigen
Unigen is a global technology company providing innovative electronics manufacturing and product solutions to customers across diverse industries. With decades of industry experience and operations in key global markets, we combine engineering expertise, advanced manufacturing capabilities, and responsive customer service to deliver reliable, high-quality solutions—from product development through production and fulfillment.

Location and Work Arrangement
This position is based in Newark, California and is onsite.

Benefits
Unigen offers a competitive compensation and benefits package, including medical, dental, and vision coverage; a 401(k) plan; paid time off; paid holidays; and professional development opportunities. Benefits are subject to eligibility requirements and applicable plan terms.

Job Title: Quality System Specialist
Job Function: Quality Department
Report to: Senior Quality Assurance Engineering Manager 

Job Summary:The Quality System Specialist is responsible for developing, implementing, maintaining, and continually improving the organization’s management systems, including Quality (ISO 9001/IATF 16949/AS9100/ISO 13485), Environmental (ISO 14001), Occupational Health & Safety (ISO 45001), and Information Security (ISO 27001). This role ensures compliance with applicable standards, legal requirements, and customer expectations, and drives a culture of continuous improvement across all management systems.

Primary Job Responsibilities:

  1. Management System Development & Maintenance
  • Develop, implement, and maintain QMS, EMS, OHSMS, and ISMS in alignment with business objectives, ISO standards, regulatory requirements, and customer expectations.
  • Ensure effective integration and alignment of all management systems with core business processes.
  • Maintain accurate documentation, procedures, and records to demonstrate compliance and support internal and external audits.
  • Monitor changes in standards, regulations, and customer requirements, and update systems and processes as needed.
  • Ensure ongoing compliance with legal, regulatory, and customer-specific requirements.
  • Collaborate with relevant departments to prepare management review reports and coordinate management review meetings.
  • Work with relevant departments to establish quality objectives and Key Process Indicators (KPIs), monitor progress toward achievement, and drive continuous improvement initiatives.
  • Support effective risk assessment, hazard assessment, environmental emergency, health and safety emergency testing, and contingency testing as required by applicable management systems.
  • Respond to customer questionnaires and surveys related to applicable management systems.

      2.  Audits & Compliance

  • Coordinate with internal auditors for audits of QMS, EMS, OHSMS, and ISMS as required.
  • Track and close nonconformities, corrective actions, and preventive actions (CAPA) related to management systems.
  • Manage external audits and certification/recertification processes.
    3.Training & Awareness
  • Ensure employee awareness of applicable management systems.
  • Collaborate with relevant departments on competence training programs.
  • Promote a culture of quality, safety, environmental stewardship, and information security.
    4. Continuous Improvement
  • Participate in cross-functional teams to drive process improvements and risk reduction in the organization’s management systems.
  • Analyze data and trends to identify opportunities for improvement.
  • Support root cause analysis and problem-solving activities.
  • Others task when assigning by Manager.

Requirement and Qualification:

  • Associate's degree in related field.
  • 2+ years of experience in management systems related to manufacturing company.
  • Working knowledge of at least one of ISO 9001, ISO 14001, ISO 45001, ISO 27001, IATF 16949, AS9100, ISO 13485.
  • Experience with internal/external audits and CAPA processes.
  • Strong analytical, organizational, and communication skills.
  • Internal auditor certification of at least one of applicable management system standards.
  • Lead Auditor certification(s) preferred.