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Quality Assurance Document Control Jobs (NOW HIRING)

Real Soft, Inc.

Document Controller

Indianapolis, IN · On-site

Qualifications The experienced Document Controller supports the GQC QA Operations team by managing the full lifecycle, control, and governance of quality documentation required for compliance with ...

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

As of Jul 7, 2026, the average hourly pay for quality assurance document control in the United States is $28.56, according to ZipRecruiter salary data. Most workers in this role earn between $22.12 and $32.93 per hour, depending on experience, location, and employer.

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

To thrive as a Quality Assurance Document Control specialist, you need strong organizational skills, attention to detail, and a solid understanding of quality management systems, often supported by a degree in science or engineering. Familiarity with document management software (such as MasterControl or Veeva Vault), compliance regulations (like ISO 9001 or FDA 21 CFR Part 11), and sometimes relevant certifications are typical requirements. Strong communication, problem-solving abilities, and a commitment to accuracy make someone stand out in this position. These skills are crucial to ensure regulatory compliance, maintain document integrity, and support consistent quality standards within the organization.

What is Quality Assurance Document Control?

Quality Assurance (QA) Document Control refers to the management, organization, and maintenance of documents related to quality processes within an organization. This role ensures that all quality-related documents, such as standard operating procedures, work instructions, and records, are properly created, reviewed, approved, distributed, and archived according to regulatory and company standards. QA Document Control professionals help ensure compliance with industry regulations and facilitate audits by maintaining accurate and accessible documentation. They also play a key role in document version control and preventing unauthorized document changes.

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

AspectQuality Assurance Document ControlQuality Assurance Specialist
Primary FocusManaging and maintaining quality documentation and recordsPerforming quality inspections, audits, and ensuring product/service compliance
CredentialsOften requires certifications in document management or quality systemsTypically holds certifications like ASQ CQE or ISO auditor
Work EnvironmentOffice-based, document management systems, quality departmentsManufacturing, labs, or field environments
Industry UsageCommon in regulated industries like aerospace, healthcare, manufacturingApplied across similar industries for quality assurance tasks

While both roles support quality objectives, Quality Assurance Document Control focuses on managing quality records and documentation, ensuring compliance and traceability. In contrast, a Quality Assurance Specialist actively performs inspections, audits, and process improvements to uphold product and service quality.

How does the Quality Assurance Document Control role interact with cross-functional teams during audits and compliance reviews?

In a Quality Assurance Document Control position, you will frequently collaborate with cross-functional teams such as manufacturing, regulatory affairs, and quality assurance to ensure all documentation is accurate, up-to-date, and audit-ready. During audits and compliance reviews, you play a key role by coordinating document retrieval, clarifying document histories, and supporting teams in addressing auditor queries. This collaborative environment helps you build strong working relationships and gives you a comprehensive understanding of the organization's quality systems, which is valuable for career advancement.
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Quality Assurance Document Control jobs near you
Infographic showing various Quality Assurance Document Control job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 90% Full Time, 7% Part Time, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $59,398 per year, or $28.6 per hour.
Quality Documentation Control Specialist

Quality Documentation Control Specialist

PROMED MOLDED PRODUCTS INC

Minneapolis, MN • On-site

$29.68 - $40.96/hr

Full-time

Re-posted 5 days ago

Job description

POSITION SUMMARY

The Quality Assurance Document Control Specialist is responsible for day-to-day administration, maintenance, and continuous improvement of the organization’s document control within the Quality Management System (QMS) in a regulated pharmaceutical and medical device environment. Ensuring that QMS components are accurate, current, revised, approved, accessible and archived in a compliant manner. The Quality Documentation Control Specialist ensures ProMed’s brand, philosophy, systems, policies, and procedures are properly implemented and observed.


ESSENTIAL DUTIES & RESPONSIBILITIES

Position duties and responsibilities include, but are not limited to the following:


  • Administer the operations of the document control system, including issuance, revision, approval routing, and archiving of controlled documents (SOPs, work instructions, forms, specifications, and quality records);
  • Maintain document master lists and revision histories to ensure all controlled documents reflect the current approved version;
  • Manage physical and/or hybrid document distribution, including retrieval and destruction of obsolete documents from points of use;
  • Process document change requests, track change history, and support change impact assessments in collaboration with subject matter experts (SMEs);
  • Assign and maintain document numbering schemes, version control conventions, and document retention schedules consistent with site SOPs and regulatory requirements;
  • Ensure document templates are standardized, current, and compliant with applicable regulatory and quality standards;
  • Oversee the creation, review, approval and distribution of controlled documents, including SOPs, policies, forms and work instructions with ALCOA principles;
  • Maintains the documentation files in compliance with ISO 13485. FDA 21 CFR 820
  • and 21 CFR Part 11;
  • Manage electronic and physical document repositories;
  • Support the periodic review process for controlled documents, notifying document owners of upcoming review dates and coordinating timely completion;
  • Coordinate training assignments for new and revised documents, ensuring training records are completed and filed in a timely manner as applicable;
  • Inputs data to create and revise material and method masters in the ERP system.

OTHER RESPONSIBILITIES

  • Identify and escalate gaps, inconsistencies, or potential compliance risks within the QMS to the QA Manager;
  • Participate in internal audits and self-inspections as assigned; support corrective action follow-up activities;
  • Support the implementation of regulatory changes and quality system improvements as directed;
  • Assist in preparing responses to audit observations or regulatory findings that involve document or records management.


QUALIFICATION, EDUCATION & EXPERIENCE

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.


Required:

  • Bachelor’s degree in Life Sciences, Chemistry, Engineering, or a related field;
  • 0-2 years of experience in a regulated industry (pharma, biotech, or medical device);
  • Working knowledge of GMP principles and FDA regulatory requirements (21 CFR Parts 210/211 and/or 820);
  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook).

Preferred:

  • Familiarity with eQMS platforms (e.g., MasterControl, Veeva Vault, Agile) even if primary system is paper-based;
  • Experience with ISO 13485 quality management principles;
  • Knowledge of ALCOA+ data integrity principles;
  • Ability to work autonomously, effectively manage time and deliver results on time;
  • Attention to detail and commitment to data integrity and accuracy in all quality records;
  • Effective written and verbal communication skills; ability to clearly document processes, decisions, and deviations;
  • Strong organizational skills with the ability to manage multiple priorities, deadlines, and document workflows simultaneously;
  • Collaborative mindset with the ability to work cross-functionally with operations, R&D, and other QA functions;
  • Comfort working in a structured, compliance-driven environment with defined SOPs and change control requirements;
  • Proactive problem-solving skills; escalates issues appropriately and follows through on assigned action items;
  • Aptitude for learning and applying regulatory requirements and quality standards.


WORK ENVIRONMENT

The work environment characteristics described here are representative of those an employee encounters while performing the principal roles and responsibilities of this job:

  • Exposure to heated/air conditioned, ventilated facilities with florescent lighting;
  • Exposure to building where a variety of chemical substances are used for cleaning, and/or operation of equipment;
  • The noise level in the work environment is usually minor;
  • Duties are performed indoors;
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

PHYSICAL, SENSORY, COGNITIVE & NEUROLOGICAL DEMANDS

While performing the duties of this job:

  • The employee may be required to stoop, bend, squat, kneel, reach, stand, walk, lift, pull, push, grasp, talk, hear, see and use repetitive motions;
  • Specific vision abilities required include close vision such as to read handwritten or typed material and the ability to adjust focus;
  • The position requires the individual to meet multiple demands from several people and interact with internal and external people;
  • Employee moves about the building and be able to maneuver in tight spaces between desks, etc.;
  • Employee may have duties involving walking on even or uneven surfaces;
  • Employee occasionally to frequently use a whiteboard, which can require grasping whiteboard pens, reaching at, below, or above shoulder height and may require trunk or neck rotation to look back;
  • Employee may use computers, overhead projectors, TV, and other work-related equipment, which may require an approximately 25+ pound force to push or pull equipment;
  • It is necessary to grasp and manipulate pens, markers, scissors, staplers, etc. occasionally to frequently;
  • Employee must see and hear on a continuous basis as well as speak frequently;
  • Position varies from standing, sitting, walking, etc. On some occasions it may be necessary to move quickly, run, etc. over smooth or uneven surfaces.

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