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Quality Assurance Document Control Associate Jobs

Oklo

Project Quality Assurance Manager

Santa Clara, CA · On-site +1

... document control, records, turnover, and operations-readiness work. This role helps ensure project ... Provide QA oversight of construction execution, including work package readiness, field ...

Oklo

Project Quality Assurance Manager

Santa Clara, CA · On-site

... document control, records, turnover, and operations-readiness work. This role helps ensure project ... Provide QA oversight of construction execution, including work package readiness, field ...

AVANTech, LLC

Quality Assurance Associate II

Columbia, SC · On-site

$22 - $27/hr

We are seeking an experience Quality Control Associate II to join our team in the Quality Assurance Department. A Day in the Life: * Handle QA records and quality-related documents under explicit ...

Pacelabs

PLS Document Control Specialist

Oakdale, MN

$40K - $45K/mo

This is an onsite, full-time, PLS Document Control Specialist position located in Oakdale, MN ... Quality Assurance Specialist I Pace Analytical Life Sciences (PLS) is an industry leading contract ...

New

FullSteam

Document Control Specialsit

Irving, TX · On-site

$70 - $80K/day

Associate or bachelor's degree in food science, Quality Assurance, Business Administration, or related field preferred. * 2-4 years of document control experience, preferably in a food manufacturing ...

System One

Document Controller

Indianapolis, IN · On-site

$34.94 - $41.11/hr

Owns and manages the end-to-end document control lifecycle for QA documentation, including creation, revision, review, approval, issuance, archiving, and retirement, in compliance with GQS and LQS ...

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Quality Assurance Document Control Associate information

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How much do quality assurance document control associate jobs pay per hour?

As of Jul 20, 2026, the average hourly pay for quality assurance document control associate in the United States is $26.49, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $33.65 per hour, depending on experience, location, and employer.

What is a Quality Assurance Document Control Associate?

A Quality Assurance Document Control Associate is responsible for managing, organizing, and maintaining documentation related to quality assurance processes within an organization. They ensure that all quality documents, such as standard operating procedures (SOPs), work instructions, and records, are accurate, up-to-date, and comply with regulatory requirements. Their role often involves reviewing, issuing, archiving, and tracking documents, as well as supporting audits and ensuring that employees use the correct versions of documents. This position is critical in industries like pharmaceuticals, biotechnology, and manufacturing, where document control is vital for regulatory compliance and quality management.

What are the main challenges Quality Assurance Document Control Associates face when managing document version control in regulated industries?

Quality Assurance Document Control Associates often encounter challenges ensuring all documents are current, accurate, and accessible to authorized personnel, especially in highly regulated industries like pharmaceuticals or medical devices. Managing version control requires meticulous attention to detail to prevent outdated documents from being used in production or audits. Additionally, coordinating timely reviews and approvals from multiple stakeholders can be complex, making strong organizational and communication skills essential for success in this role.

What are the key skills and qualifications needed to thrive as a Quality Assurance Document Control Associate, and why are they important?

To thrive as a Quality Assurance Document Control Associate, you need strong organizational skills, attention to detail, and familiarity with regulatory requirements, often supported by a degree in life sciences or a related field. Proficiency with document management systems (DMS), electronic quality management systems (eQMS), and standards such as ISO or FDA regulations is crucial. Effective communication, time management, and the ability to work meticulously under deadlines are valuable soft skills for this role. These competencies ensure the accuracy, compliance, and efficient handling of critical documentation, which is essential for maintaining quality standards in regulated industries.

What is the difference between Quality Assurance Document Control Associate vs Quality Assurance Specialist?

AspectQuality Assurance Document Control AssociateQuality Assurance Specialist
Primary RoleManage and maintain quality documentation, ensure document accuracy, control revisionsDevelop, implement, and monitor quality assurance processes and procedures
Required CredentialsTypically a high school diploma or associate degree; familiarity with document management systemsBachelor's degree in quality, engineering, or related field; certifications like CQE often preferred
Work EnvironmentOffice setting, regulated industries like pharmaceuticals, manufacturingLaboratory, manufacturing, or quality assurance departments in similar industries
Key FocusDocument control, compliance, record keepingProcess improvement, quality audits, compliance management

While both roles support quality assurance, the Document Control Associate primarily handles documentation and record management, whereas the Quality Assurance Specialist focuses on developing and overseeing quality processes. The Associate role is more administrative, while the Specialist role involves active process improvement and compliance oversight.

What cities are hiring for Quality Assurance Document Control Associate jobs? Cities with the most Quality Assurance Document Control Associate job openings:
What are the most commonly searched types of Quality Assurance Document Control jobs? The most popular types of Quality Assurance Document Control jobs are:
What states have the most Quality Assurance Document Control Associate jobs? States with the most job openings for Quality Assurance Document Control Associate jobs include:
Quality Assurance Document Control Associate jobs near you
Manufacturing Quality Coordinator II - Document Control Specialist

Manufacturing Quality Coordinator II - Document Control Specialist

Ryder

Provo, UT • On-site

$25.50/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 14 days ago

Ryder rating

7.2

Company rating: 7.2 out of 10

Based on 510 frontline employees who took The Breakroom Quiz

183rd of 356 rated logistics

Job description

Ryder is immediately hiring a Permanent Full Time Quality Coordinator (Document Control) at our manufacturing facility in Provo, Utah.

Warehouse positions pay Weekly!

  • Hourly Pay: $25.50+ depending upon experience/certifications
  • Schedule: Monday - Friday, 8:00 AM - 5:00 PM
  • Requirements: 3 years of quality assurance experience with document control within a food manufacturing facility 

Apply Here with Ryder Today

Click here to see and hear it from a Ryder Manufacturing Employee:

https://RyderCareers.Video/Quality-Inspect

This position is responsible for ensuring quality expectations including, but not limited to employee safety, food safety, sanitation and quality systems.

We want the right Quality Coordinator II to join us at Ryder and work with State of the Art Equipment in the Safest Warehouse Environment

  • Products Being Handled: Food & Supplements
  • Equipment: Computer, Scanner, Tablet, Scale
  • Job Duties:
    • Create and maintain documents and records relating to the quality system (specifications, Master Manufacturing Records, change control, deviations, material disposition forms)
    • Collects and reviews supplier approval documents
    • Assists with internal audits
  • Requirements: 
    • 3 or more years of QA/Document Control experience in the food and or/dietary supplement industry 
    • Skilled using Microsoft Word and Excel

Various warehouse fulfillment specialist roles at Ryder support distribution across the US. Apply here with Ryder today!

We have all benefits other Warehouse Distribution Facilities offer WITHOUT the WAIT!

  • Warehouse Positions Pay Each Week
  • On the Job Paid Training
  • Medical, Dental, Vision, 401 K etc. Start at 30 Days
  • Paid Time Off
  • 401 K offers a company match
  • HIGH VALUED Stock at 15 % Employee Discount
  • Employee Discounts that save you money on Tools, Cars, Hotels, Electronics/Appliances, Cell Phones, Travel, and muchmore
  • Safety Gear PROVIDED
  • Safety is Always the First Priority
  • State of the Art Equipment and Caring Leadership

Your drive. Your career. Start driving your future with Ryder today. Click Here to See All Ryder Careers: https://jobs.ryder.com/jobs/

We want YOU to join our family made up of Proud Women and Men in Supply Chain who work alongside the many Military Reserve and Veterans we hire everyday

EEO/AA/Female/Minority/Disabled/Veteran

Our Culture & Commitment:
At Ryder, you’re trusted to make an impact—while enjoying room to grow and having a voice that’s heard. Our culture is built on respect, collaboration, and shared pride in doing great work rooted in innovation and safety.

Your Voice. Your Success. The Future We Build Together.


  • Associate's Degree preferred
  • High school diploma required
  • Previous experience in food grade facility
  • Experience with GMPs, FDA, USDA, etc.
  • Excellent written and verbal communication skills

Important Note: Some positions require additional screening that may include employment and education verification; motor vehicle records check and a road test; and/or badging or background requirements of the customer to which you are assigned.


  • Verify and monitor relevant finished packaging codes as it relates to specifications 
  • Assist in effectively inspecting product for quality issues and remove defects/contaminants such as stones, wood, glass, plastic, etc., prior to packaging in accordance to specifications 
  • Perform timely checks to meet specifications
  • Provide supervisors/managers with proper quality documentation as required
  • Maintain Good Manufacturing Practices (GMPs) with emphasis on safety 
  • Maintain qualify to meet all standards required by FDA, USDA, etc. 
  • Ensure product quality to meet Customer, state and federal guidelines 
  • Other duties as required or assigned

 Ryder is proud to be an Equal Opportunity Employer and Drug Free workplace. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

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