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Quality Assurance Document Control Associate Jobs in California

Quality Assurance Associate

San Diego, CA ยท On-site

$24 - $33/hr

Quality Assurance Associate - Document Control, Training, and Asset Management Job Purpose The Quality Assurance Associate supports the effective operation of the Quality Management System through ...

Quality Assurance Associate

San Diego, CA ยท On-site

$24 - $33/hr

Quality Assurance Associate - Document Control, Training, and Asset ManagementJob PurposeThe Quality Assurance Associate supports the effective operation of the Quality Management System through ...

Summary: Creation and maintenance of assembly and customer documentation within the facility, in ... These systems may include, but are not limited to, quality, the environment, health, safety and ...

Summary: Creation and maintenance of assembly and customer documentation within the facility, in ... These systems may include, but are not limited to, quality, the environment, health, safety and ...

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Maintain organized and secure document control systems in accordance with company and customer ... Associate's or Bachelor's degree in a related field preferred. * Minimum of 4 years of experience ...

Be Seen First

Maintain organized and secure document control systems in accordance with company and customer ... Associate's or Bachelor's degree in a related field preferred. * Minimum of 4 years of experience ...

Support audits, quality assurance reviews, and records management compliance assessments. * Resolve document control issues, administrative challenges, and workflow bottlenecks to maintain project ...

Support audits, quality assurance reviews, and records management compliance assessments. * Resolve document control issues, administrative challenges, and workflow bottlenecks to maintain project ...

Support audits, quality assurance reviews, and records management compliance assessments. * Resolve document control issues, administrative challenges, and workflow bottlenecks to maintain project ...

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Quality Assurance Document Control Associate information

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 key skills and qualifications needed to thrive as a quality assurance document control associate?

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 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 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 are the most commonly searched types of Quality Assurance Document Control jobs in California?

The most popular types of Quality Assurance Document Control jobs in California are:

What cities in California are hiring for Quality Assurance Document Control Associate jobs?

Cities in California with the most Quality Assurance Document Control Associate job openings:

QA Document Control Coordinator

Sacramento, CA โ€ข On-site

Full-time

Re-posted 23 days ago


Job description

Job Summary:The QA Document Control Coordinator is responsible for maintaining, organizing, and controlling quality assurance documentation to ensure compliance with food safety programs, regulatory requirements, customer standards, and company procedures. This role supports the Quality Assurance department by ensuring accurate records, proper document control, audit readiness, and timely updates to quality and food safety documentation.Job Duties:Quality Assurance – Document Control (Primary Focus)• Maintain and control QA documentation, including SOPs, SSOPs, forms, logs, specifications, policies, and quality records.• Ensure proper document version control, approval processes, revisions, and distribution of updated documents.• Organize and maintain electronic and physical filing systems for quality and food safety records.• Coordinate document retention and archiving in compliance with regulatory, customer, and company requirements.• Support internal audits and third-party audits, including SQF, BRCGS, FDA, customer, and certification audits.• Maintain audit documentation and ensure records are organized, accurate, and readily available.• Track corrective actions, preventive actions (CAPA), and compliance records.• Assist with updating food safety plans, quality manuals, procedures, and related documentation.• Review documents for accuracy, completeness, and compliance with established requirements.• Maintain and update quality system records, including training records, inspection records, and other compliance documentation.• Assist Quality Assurance personnel with data collection, reporting, record review, and document preparation.• Support continuous improvement initiatives related to food safety, quality systems, and documentation practices.• Maintain confidentiality of company records and quality information.• Perform other duties as assigned or otherwise identified.Knowledge, Skills and Qualifications:• Associate or bachelor’s degree preferred (Food Science, Quality Assurance, Business Administration, or related field).• 2+ years of experience in quality assurance, document control, food manufacturing, or related administrative roles preferred.• Experience working in a food manufacturing environment strongly preferred.• Practical knowledge and experience with food safety and quality systems, including SQF, BRCGS, HACCP, GMP, FDA requirements, and third-party audit processes preferred.• Experience supporting GFSI-certified facilities and maintaining audit-ready documentation is highly desirable.• Experience with SOP management, document control systems, quality records, corrective actions, and compliance documentation preferred.• Strong computer skills, including Microsoft Office and document management systems.• High attention to detail and accuracy.• Strong organizational skills and ability to maintain accurate and complete records.• Ability to manage multiple priorities and meet deadlines in a fast-paced manufacturing environment.• Ability to work independently with minimal supervision.• Strong written and verbal communication skills.• Ability to identify discrepancies, investigate issues, and support implementation of corrective actions.• Ability to handle confidential company information with discretion.• Strong problem-solving skills and attention to detail.• Ability to effectively communicate and collaborate with Quality Assurance, Operations, Production, Maintenance, and other departments.• Reliable, organized, and committed to maintaining a safe and positive work environment.Minimum Experience Requirement:Applicants should have previous experience in Quality Assurance, Document Control, Food Safety, or a related role within a food manufacturing environment. Candidates without experience with quality systems, food safety documentation, audit preparation, or document control responsibilities are encouraged not to apply. Interaction/Supervision:This position interacts with Quality Assurance, Operations, Production, Maintenance, and other departments as needed. This role requires collaboration with internal teams and external auditors or customers to support compliance, document management, and quality system requirements. This position does not have direct supervisory responsibilities.Typical Working Environment:Work is performed indoors in both an office and food manufacturing environment. The position requires computer work, document review, record management, and periodic movement throughout the facility to support quality activities. The work environment may include moderate noise levels consistent with a food production facility.Equipment/Tools Used:Computer, keyboard, phone, tablet/iPad, multifunction printer/copier, document management systems, and other miscellaneous office equipment.Physical Demands:Constantly (More than 66% of the time):• Sitting, computer work, reviewing documents, data entry, and record management.Frequently (34-66%):• Walking through the facility, communicating with employees, and reviewing quality records.Occasionally (1-33%):• Standing, bending, reaching, lifting or moving documents/materials, and participating in facility activities.Rarely (less than 1 hour per week):• Additional physical activities as required by business needs. Hours of Work:This position will work the hours necessary to meet the needs of the business and complete required job duties. Work may occasionally include additional hours based on operational needs, audits, inspections, or compliance requirements.Employee is authorized and permitted to take all meal and rest breaks in accordance with company policy and applicable regulations.The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties, and skills required. Management reserves the right to modify, reassign, or alter duties as dictated by business necessity and reasonable accommodation requirements.