Document Controller

The Document Controller / Documentation Coordinator prepares, organizes, and maintains documentation related to quality assurance and quality control systems. This role supports the implementation and maintenance of ISO 9001 standards, performs ISO audits as needed, and leads the conversion of existing quality documentation into a new Quality Management System (QMS). The position combines hands-on document control, data analysis, and close collaboration with the quality department in a manufacturing environment.

• Prepare, organize, and maintain documentation related to quality assurance and quality control systems within the QMS.
• Create, retrieve, and electronically organize documentation for the QMS system to ensure accuracy, consistency, and accessibility.
• Collect, review, route for approval, and publish standard operating procedures (SOPs), work instructions (WIs), and test procedures.
• Maintain and update a database for external documentation, including standards and specifications, ensuring that the latest revisions are available and properly controlled.
• Convert existing quality documentation into the new QMS system, ensuring proper formatting, version control, and alignment with ISO 9001 requirements.
• Create PDF files and other electronic document formats as needed to support quality documentation and distribution.
• Perform ISO audits as needed, supporting audit planning, documentation review, and follow-up actions.
• Conduct data analysis on quality key performance indicators (KPIs) and prepare clear, concise presentations based on the data.
• Collaborate with the quality department and other stakeholders to write and update work instructions, SOPs, and other quality documents.
• Support quality assurance and quality control activities by ensuring documentation meets internal and external standards.
• Ensure all documentation activities comply with company health and safety procedures and relevant quality standards.
• Communicate with manufacturing and other departments as needed to gather information, clarify requirements, and resolve documentation-related questions.

• At least 4 years of experience working with ISO 9001 and ISO standards.
• At least 4 years of experience in a manufacturing setting.
• Experience working in a quality department, supporting quality assurance and quality control activities.
• Hands-on experience with Quality Management Systems (QMS), including document creation, organization, and control.
• Proficiency in writing and maintaining work instructions, SOPs, and test procedures.
• Strong document control experience, including version control, approvals, and electronic filing.
• Knowledge of ISO standards and ISO 9001 requirements as they relate to documentation and quality systems.
• Proficiency with Excel for data analysis and reporting.
• Ability to perform data analysis on quality KPIs and develop clear presentations from the findings.
• Strong attention to detail and accuracy in preparing and reviewing documentation.
• Ability to understand and follow company health and safety procedures.

• Experience converting existing documentation into a new QMS platform.
• Experience performing or supporting ISO audits.
• Familiarity with quality assurance and quality control methodologies in a manufacturing environment.
• Strong organizational skills and the ability to manage multiple documents and tasks simultaneously.
• Effective communication skills for collaborating with quality, manufacturing, and other departments.
• Ability to work independently while maintaining alignment with quality and compliance requirements.

The role is based in an office environment within a manufacturing facility and involves working closely with one other manager. The position primarily operates in the office, focusing on electronic document management and data analysis, with occasional visits to the shop floor as needed to gather information or ask questions. The work involves regular use of computers, office productivity software such as Excel, and QMS tools for document control and data reporting. The environment follows established health and safety procedures, and the role supports a structured, quality-focused culture.

This is a Contract position based out of Sugar Land, TX.

The pay range for this position is $30.00 - $34.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Sugar Land,TX.

This position is anticipated to close on Sep 18, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email for other accommodation options.

San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.