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Qa Associate Specialist Document Control Jobs in Riverside, CA

... Control, Operations, Procurement, Sales, Customer Service, and the China Office to ensure products ... Quality Assurance & Regulatory Staff (US) Documentation and Quality Assurance Specialist Staff ...

... and Document Control Specialist. • Leads Continuous Improvement of processes integral to product quality and scrap. • Improves quality assurance systems company-wide to achieve zero defects ...

... and Document Control Specialist. • Leads Continuous Improvement of processes integral to product quality and scrap. • Improves quality assurance systems company-wide to achieve zero defects ...

... Control, Operations, Procurement, Sales, Customer Service, and the China Office to ensure products ... Staff (US) • Documentation and Quality Assurance Specialist Staff (China) Primary ...

Quality Assurance Specialist Location: Pomona, California Duration: 12 Months 100% Onsite Summary ... change control, quality documentation, and compliance activities under the supervision of the ...

Document Control Clerk

Anaheim, CA · On-site

$17 - $19/hr

Document Control Clerk Location: Anaheim, CA Schedule: Monday-Friday, 12:30pm - 9:00pm Pay: $17.00 ... Identify and report quality concerns to ensure the highest level of accuracy * Collaborate with ...

Description Document Control Clerk Location: Anaheim, CA Schedule: Monday-Friday, 12:30pm - 9:00pm ... Identify and report quality concerns to ensure the highest level of accuracy * Collaborate with ...

Document Control Clerk

Anaheim, CA · On-site

$17 - $19/hr

Document Control Clerk Location: Anaheim, CA Schedule: Monday-Friday, 12:30pm - 9:00pm Pay: $17.00 ... Identify and report quality concerns to ensure the highest level of accuracy * Collaborate with ...

QA/QC Specialist

Brea, CA · On-site

$27 - $33/hr

Act as a key liaison with food safety and quality assurance teams at major retail partners to ... Manage documentation and compliance for food safety systems such as FSVP and other country-specific ...

Maintain test plans, certification documentation, and continuously improve QA processes. Provide ... Associate's degree in Business, Communications, Education, Engineering, or related field, Food or ...

Showing results 21-40

Qa Associate Specialist Document Control information

See Riverside, CA salary details

$11

$27

$48

How much do qa associate specialist document control jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for qa associate specialist document control in Riverside, CA is $27.63, according to ZipRecruiter salary data. Most workers in this role earn between $19.33 and $35.10 per hour, depending on experience, location, and employer.

What does a QA associate specialist document control do?

A QA Associate Specialist in Document Control is responsible for managing and maintaining quality assurance documents within an organization, particularly in regulated industries like pharmaceuticals or biotechnology. Their duties include organizing, reviewing, distributing, and archiving documents to ensure compliance with regulatory standards and company policies. They also help implement document control procedures, support audits, and ensure all documents are up-to-date and accessible to authorized personnel. This role is crucial for maintaining data integrity and supporting continuous improvement in quality systems.

What are the key skills and qualifications needed to thrive as a QA associate specialist document control?

To thrive as a QA Associate Specialist Document Control, you need a strong understanding of quality assurance principles, regulatory requirements (such as GMP or ISO standards), and document management, often supported by a relevant degree or equivalent experience. Familiarity with electronic document management systems (EDMS), quality management software, and document version control tools is typically required. Attention to detail, organizational skills, and effective communication enable success in managing documentation and collaborating with cross-functional teams. These skills ensure the integrity, compliance, and accessibility of critical documents, supporting regulatory readiness and operational excellence.

What are some common challenges faced by a QA associate specialist document control, and how can they be managed effectively?

One common challenge for QA Associate Specialists in Document Control is ensuring timely and accurate processing of large volumes of documents while maintaining strict compliance with regulatory standards. Balancing the need for efficiency with the necessity for thoroughness can be demanding, especially during audits or product launches. Effective use of document management systems, strong organizational skills, and clear communication with cross-functional teams help manage these challenges. Additionally, staying proactive about training and regulatory updates is key to minimizing errors and maintaining high-quality standards.

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

AspectQa Associate Specialist Document ControlQa Associate Specialist Quality Assurance
Primary FocusManaging and controlling documentation, ensuring document accuracy and complianceEnsuring product quality through testing, inspections, and process audits
Key ResponsibilitiesDocument review, version control, record keepingProduct testing, process validation, quality audits
Required CredentialsTypically a degree in life sciences or related field, familiarity with document management systemsSimilar educational background, knowledge of quality standards and testing procedures
Work EnvironmentOffice-based, document management systems, regulated industriesLaboratory or manufacturing settings, quality labs

While both roles support quality processes, the Qa Associate Specialist Document Control primarily manages documentation and records, whereas the Qa Associate Specialist Quality Assurance focuses on product testing and process validation. Both positions require similar credentials and are essential in regulated industries like pharmaceuticals and biotech.

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For Qa Associate Specialist Document Control jobs in Riverside, CA, the most frequently searched job titles are:

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The top searched job categories for Qa Associate Specialist Document Control jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Qa Associate Specialist Document Control jobs?

Cities near Riverside, CA with the most Qa Associate Specialist Document Control job openings:

Infographic showing various Qa Associate Specialist Document Control job openings in Riverside, CA as of July 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $57,474 per year, or $27.6 per hour.

Quality Assurance & Regulatory Manager

Irvine, CA • On-site

Nura
Food Services and Drinking Places • 11 - 50 employees

Full-time

Re-posted 7 days ago


Job description

The Quality Assurance & Regulatory Manager provides leadership and day-to-day management of NURA's Quality

Assurance and Regulatory functions while supporting the strategic direction established by the Director of Quality. This roleis responsible for maintaining and continuously improving the Quality Management System (QMS), regulatory complianceprograms, supplier qualification, customer technical support, documentation systems, and ingredient safety initiatives.


The position leads the Quality Assurance and Regulatory team while partnering closely with Quality Control, Operations,

Procurement, Sales, Customer Service, and the China Office to ensure products consistently meet regulatory requirements,customer expectations, and NURA's quality standards.


Reporting directly to the Director of Quality, this position translates strategic initiatives into day-to-day execution, develops departmental talent, drives continuous improvement, and serves as the primary leader for Quality Assurance and Regulatoryactivities.


Direct Reports:

Quality Assurance & Regulatory Staff (US)

Documentation and Quality Assurance Specialist Staff (China)


Primary Responsibilities:

Quality Management Leadership

Lead the Quality Assurance, Documentation, and Regulatory departments in both the US and China Offices,

establishing priorities, workload, and performance expectations.

Manage and continuously improve NURA's Quality Management System (QMS). NURA's QMS includes but is not

limited to (NURA & Manufacturer Certification Maintenance, Ingredient and Supplier Quality Documentation,

Complaint Handling & Resolution, Ingredient/Manufacturer/Facility regulatory documentation., etc.)

Establish departmental KPIs and monitor performance against quality objectives.

Lead management review activities and quality performance reporting.

Drive continuous improvement initiatives using data and risk-based decision making.

Standardize quality processes across U.S. and China operations.

Ensure quality and regulatory activities are executed proactively, with clear ownership, timely communication, and

defined completion timelines.


Regulatory & Compliance

Ensure compliance with FDA, FSMA, FSVP, USDA Organic, Non-GMO Project, Kosher, Halal, SQF, customer-specific

requirements, and other applicable regulations.

Oversee regulatory documentation, technical documentation, and customer compliance requests.

Review regulatory changes and implement appropriate internal actions.

Lead regulatory assessments for new products and suppliers.

Serve as the primary internal resource for regulatory interpretation and customer regulatory inquiries.


Supplier Quality Management

Oversee the FSVP Program at NURA ensuring qualification activities are being maintained, documentation and

assessments are being performed according to established SOPs, and compliance gaps are addressed immediately.

Approve supplier qualification activities.

Review supplier audits, risk assessments, CAPAs, and performance metrics.

Drive supplier quality improvement initiatives.

Escalate supplier quality concerns and monitor corrective actions.


Customer Quality Support

Oversee customer questionnaires, technical documentation, specifications, COAs, allergen statements, regulatory

forms, and certification requests, ensuring proper checks are in place and systematic improvement efforts are

implemented to ensure documentation is current, accurate, and professionally answered.

Lead customer audits and quality meetings.

Provide technical guidance to Sales and Customer Service.

Lead customer complaint investigations requiring Quality Assurance involvement ensuring prompt response,

effective root cause analysis, corrective actions, and document closure.


Documentation & Quality Systems

Ensure all controlled documents remain accurate, current, and compliant.

Approve SOPs, work instructions, forms, and quality records.

Lead document control, change control, and document retention programs.

Improve document workflows and digital quality systems.

Ensure consistency and version control across all technical documentation distributed internally and externally.
Product Safety & Risk Management

Maintain HACCP, Food Safety Plan, Food Defense, Recall, Traceability, and Risk Assessment programs.

Lead internal audits and regulatory inspections.

Coordinate external certification audits.

Ensure corrective and preventive actions are implemented effectively.


Team Leadership

Recruit, coach, mentor, and develop Quality Assurance and Regulatory personnel.

Conduct performance reviews and establish employee development plans.

Foster accountability, ownership, urgency, collaboration, and continuous learning.

Build cross-functional partnerships throughout the organization.

Foster accountability, ownership, urgency, collaboration, professionalism and a proactive mindset.


Cross-Functional CollaborationPartner closely with:

Quality Control

Purchasing

Logistics

Warehouse Operations

Sales

Customer Service

China Office

Executive Leadership


Decision-Making Authority

Approve supplier qualification status.

Approve controlled quality documents.

Approve regulatory documentation.

Approve quality investigations and CAPAs.

Recommend supplier disqualification when appropriate.
Recommend product disposition for quality-related issues.

Escalate significant business risks to the Director of Quality & Regulatory.


Key Performance Indicators:

Audit Performances (Internal and External facilities). Successfully manage internal audits, supplier audits, customer

audits, and third-party certification audits, with timely closure of findings and corrective actions.

Complaint Closure Turn Around Time and Customer Management. Ensure customer complaints, investigations, root

cause analysis, and corrective actions are completed accurately, communicated appropriately, and closed within

established timeline.

Document and Technical Requests closure time. Ensure customer questionnaires, specifications, regulatory

documents, certifications, and technical requests are completed accurately, consistently, and within established

turnaround times.

Manufacturer engagement and development. Supplier qualification completed on schedule and supplier quality

issues resolved.


Leadership:

Team engagement

Employee development

Cross-functional collaboration

Implementation of continuous improvement initiatives.


Qualifications

Education:Bachelor's degree in Food Science, Microbiology, Chemistry, Biology, Regulatory Affairs, Quality Assurance, or relateddiscipline.


Experience

5+ years in Quality Assurance or Regulatory Affairs within food, dietary supplements, or ingredient

manufacturing/distribution.

2+ years leading Quality or Regulatory teams.

Strong working knowledge of FDA, FSMA, FSVP, GMPs, HACCP, and supplier quality systems.

Experience managing customer audits and regulatory inspections.

Experience developing and improving Quality Management Systems.

Demonstrated experience using TraceGains for supplier qualification, document management, and customer

technical documentation.
Core Competencies

Leadership & Coaching

Strategic Thinking

Regulatory Expertise

Quality Systems Management

Supplier Qualification and Maintenance.

Risk Assessment

Root Cause Analysis

CAPA Management

Customer Management

Project Management

Cross-Functional Leadership

Continuous Improvement

Strong Communication

Data-Driven Decision Making

Change Management

Execution and Accountability