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Quality Control Associate Jobs in Tracy, CA (NOW HIRING)

Alcon3Pl

QA Associate - Livermore, CA

Livermore, CA · On-site

$26 - $30/hr

QA Associate - Livermore, CA Lobos Staffing is hiring a QA Associate for a temp-to-perm opportunity ... Knowledge of GMPs, HACCP, allergens, food safety, and quality control . * Strong organizational ...

Gexpro Services

Quality Inspector

Livermore, CA · On-site

Manages QC equipment for 3rd party calibration and Non-Conforming Material Receipt (NCMR) Cage ... Associate Degree/Trade School (2 yr. min.) in Quality/Material Composition, Non-Destructive testing ...

Gexpro Services

Quality Inspector

Livermore, CA · On-site

The ideal candidate for the Quality Inspector will have Quality Control (QC) experience. This ... Associate Degree/Trade School (2 yr. min.) in Quality/Material Composition, Non-Destructive testing ...

DHL Germany

Quality Assurance Supervisor

Modesto, CA · On-site

$70.30 - $90/hr

Supervise, coach, and train hourly associates supporting quality assurance and control activities (e.g. Operators, QA Tech I, QA Tech II, etc). * Other duties as assigned. Required Education and ...

New

DPDHL

Quality Assurance Supervisor

Modesto, CA · On-site

$55K - $90K/yr

Supervise, coach, and train hourly associates supporting quality assurance and control activities (e.g. Operators, QA Tech I, QA Tech II, etc) * Other duties as assigned Required Education and ...

DHL

Quality Assurance Supervisor

Modesto, CA · On-site

$55K - $90K/yr

Supervise, coach, and train hourly associates supporting quality assurance and control activities (e.g. Operators, QA Tech I, QA Tech II, etc) * Other duties as assigned Required Education and ...

Gexpro Services

Receiving Associate

Livermore, CA · On-site

$22/hr

Stage materials in designated areas for Quality Control (QC) inspections. * Load and unload trucks ... Receiving Associate Requirements: The Receiving Associate should preferably possess a high school ...

Pratt Industries

Quality & Safety Tech

Stockton, CA

$18.25 - $24.50/hr

Control of non-conforming supplier defects and returns * Management of sorting and reworks ... associate (two-year) college degree. * Minimum of one years of experience in a related field and ...

Pratt Industries

Quality & Safety Tech

Stockton, CA · On-site

$18.25 - $24.50/hr

Control of non-conforming supplier defects and returns * Management of sorting and reworks ... associate (two-year) college degree. * Minimum of one years of experience in a related field and ...

Grifols

Assistant Chemist / Associate Chemist

Clayton, CA · On-site

$26.25 - $34.50/hr

Clayton, North Carolina Assistant Chemist / Associate Chemist Performs chemical testing of moderate to advanced complexity within a Quality Control Laboratory in a safe, accurate, and efficient ...

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Showing results 21-40

All JobsQuality Control Associate JobsQuality Control Associate Jobs in Tracy, CA

Quality Control Associate information

See Tracy, CA salary details

$12

$27

$41

How much do quality control associate jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for quality control associate in Tracy, CA is $27.41, according to ZipRecruiter salary data. Most workers in this role earn between $19.90 and $33.37 per hour, depending on experience, location, and employer.

What does a quality control associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

What are the key skills and qualifications needed to thrive as a quality control associate?

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges quality control associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

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

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

What are the most commonly searched types of Quality Control jobs in Tracy, CA?

The most popular types of Quality Control jobs in Tracy, CA are:

What cities near Tracy, CA are hiring for Quality Control Associate jobs?

Cities near Tracy, CA with the most Quality Control Associate job openings:

Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Tracy, CA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, 4% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $57,013 per year, or $27.4 per hour.

Document Control & Quality Systems Administrator

Noctrix Health

Pleasanton, CA • On-site, Remote

Full-time

Posted 9 days ago

Job description

Noctrix Health is redefining the treatment of chronic neurological disorders with clinically validated therapeutic wearables. Our team of medical device specialists, neuroscientists, and consumer electronics engineers is dedicated to delivering prescription-grade therapy with an outstanding user experience. We have pioneered the world's first drug-free wearable therapy, clinically proven to alleviate symptoms in adults with drug-resistant Restless Legs Syndrome (RLS). Join us in transforming healthcare, improving lives, and driving meaningful change through innovative medical technology.
We are seeking an experienced and highly organized Document Control & Quality Systems Administrator to manage the day-to-day administration of document control and key Quality Management System (QMS) processes at Noctrix Health. This individual will serve as the primary administrator for controlled documents, employee training records, quality records, and the electronic Quality Management System (eQMS), ensuring information remains accurate, current, traceable, compliant, and inspection-ready.
The Document Control & Quality Systems Administrator will work cross-functionally with Quality, Regulatory Affairs, Clinical Affairs, Engineering, Operations, and Manufacturing to support the effective operation of the QMS. This role will manage document lifecycle activities, training administration, calibration records, supplier documentation, record retention, finished goods documentation, and other critical quality system activities while identifying opportunities to improve efficiency and compliance.
This position reports to the Director, Quality.
This is a full-time position that may be performed remotely or in a hybrid capacity at our Pleasanton headquarters.
Responsibilities:
  • Serve as the primary administrator for Noctrix Health's document control and electronic Quality Management System (eQMS), ensuring compliance with internal procedures and applicable regulatory requirements
  • Manage the complete lifecycle of controlled documents, including formatting, routing, review, approval, issuance, revision, obsolescence, archival, and retention
  • Administer eQMS workflows, user access, system data integrity, and routine system maintenance
  • Perform and document eQMS validation activities associated with changes to document control templates, workflows, and applicable system functionality
  • Develop, maintain, and continuously improve document control procedures, templates, workflows, and related Quality System documentation
  • Administer the company's quality training program, including training assignments, completion tracking, training matrices, and electronic training records
  • Monitor training compliance and partner with department leaders to ensure required training is completed accurately and within established timelines
  • Provide training and ongoing user support for document control, training, and eQMS processes
  • Maintain calibration records and coordinate calibration activities with approved service providers to ensure equipment remains compliant with applicable requirements
  • Administer the Approved Supplier List and support the Supplier Management Program, including supplier records, qualification status, reassessments, audit schedules, and quality agreements
  • Manage Quality System records and archives in accordance with company procedures and applicable record retention requirements
  • Review Lot History Records (LHRs) for completeness and compliance with Good Documentation Practices (GDP), resolve identified documentation issues, and support finished goods release to inventory
  • Support Quality System processes including change control, Management Review, Design Reviews, CAPA, nonconformances, complaints, supplier management, audits, inspections, and validation activities
  • Prepare, organize, and maintain inspection-ready records for internal audits, supplier audits, regulatory inspections, and certification audits
  • Partner cross-functionally with Quality, Regulatory Affairs, Clinical Affairs, Engineering, Operations, and Manufacturing to ensure timely execution of Quality System activities
  • Identify and implement opportunities to improve document control and Quality System administration for greater efficiency, consistency, data integrity, and compliance
  • Provide additional Quality Systems and operational support as organizational needs evolve

Requirements:
  • Associate's or Bachelor's degree in a scientific, technical, quality, business administration, or related discipline
  • Minimum of 3 years of experience in document control, Quality Systems administration, training administration, or Quality Assurance within the medical device, biotechnology, pharmaceutical, or other regulated industry
  • Demonstrated experience administering document control systems, training systems, eQMS platforms, and Quality System records
  • Working knowledge of FDA Quality System requirements, ISO 13485, document control principles, electronic records, training management, and record retention requirements
  • Experience supporting Quality System processes such as change control, CAPA, nonconformances, supplier management, audits, inspections, or calibration programs
  • Experience maintaining accurate, traceable, and inspection-ready Quality System documentation
  • Proficiency with Microsoft Office applications and electronic Quality Management Systems
  • Strong organizational and time-management skills with the ability to independently manage multiple priorities and deadlines
  • Exceptional attention to detail with a strong commitment to documentation accuracy and data integrity
  • Strong written and verbal communication skills
  • Ability to work independently while collaborating effectively across multiple functions

Preferred Qualifications:
  • Experience within an FDA-regulated medical device organization
  • Experience with Arena or a comparable electronic Quality Management System
  • Experience serving as an eQMS administrator, system owner, or power user
  • Experience with eQMS validation, system configuration, workflow changes, or system enhancements
  • Familiarity with FDA 21 CFR Part 820, 21 CFR Part 11, ISO 13485, and Good Documentation Practices
  • Experience supporting FDA inspections, ISO certification audits, or other regulatory audits
  • Experience with supplier administration, calibration programs, and manufacturing quality records
  • Experience reviewing Lot History Records and supporting finished goods release

Compensation:
  • Base Pay: $120,000-$140,000 per year
  • Annual Bonus Eligibility

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