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Document Control Associate Jobs in Dublin, OH (NOW HIRING)

Holder Construction

Project Manager

Columbus, OH · On-site

Our structured career development program empowers associates to grow quickly into expanded roles ... document control, RFIs, submittals, scheduling, financials, and field communication. * Proven ...

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Document Control Associate information

See Dublin, OH salary details

$10

$25

$44

How much do document control associate jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for document control associate in Dublin, OH is $25.52, according to ZipRecruiter salary data. Most workers in this role earn between $17.84 and $32.40 per hour, depending on experience, location, and employer.

What is a document control associate?

Document Control Associates are professionals responsible for managing, organizing, and maintaining company documents and records. They ensure that documents are properly filed, easily accessible, and comply with regulatory standards or company policies. Their duties often include tracking document versions, distributing updated documents to relevant teams, and maintaining document security and confidentiality. This role is critical in industries such as construction, pharmaceuticals, engineering, and manufacturing, where accurate documentation is essential for compliance and quality control.

What skills and qualifications are needed to thrive as a document control associate?

To thrive as a Document Control Associate, you need strong organizational abilities, attention to detail, and a background in records management or a related field. Familiarity with document management systems (DMS), Microsoft Office Suite, and sometimes ISO or GMP compliance standards is typically required. Excellent communication, time management, and problem-solving skills help ensure accuracy and efficiency in handling sensitive documentation. These skills are crucial for maintaining data integrity, regulatory compliance, and smooth information flow within an organization.

How does a document control associate typically interact with other departments, and what collaboration skills are important for success?

As a Document Control Associate, you will regularly collaborate with various departments such as engineering, quality assurance, and project management to ensure all documentation is accurate, up-to-date, and compliant with company standards. Effective communication and organizational skills are essential, as you'll often coordinate document reviews, approvals, and distribution. Being detail-oriented and responsive helps you manage document requests efficiently, while strong teamwork skills foster smooth information flow and support cross-functional objectives.

What is the difference between Document Control Associate vs Document Coordinator?

AspectDocument Control AssociateDocument Coordinator
CertificationsOften requires familiarity with document management systems, industry-specific certificationsSimilar certifications, with emphasis on document organization and communication skills
Work EnvironmentTypically in manufacturing, engineering, or construction industriesCommonly in corporate, engineering, or technical settings
Employer & Industry UsageUsed by companies managing technical documents, quality recordsUsed in project management, quality assurance, and administrative roles

The main difference between a Document Control Associate and a Document Coordinator lies in their focus areas. The Document Control Associate primarily manages technical documents, ensuring version control and compliance, while the Document Coordinator often handles broader document workflows and communication. Both roles require similar skills and certifications but serve slightly different functions within organizations.

What cities near Dublin, OH are hiring for Document Control Associate jobs?

Cities near Dublin, OH with the most Document Control Associate job openings:

Document Control Associate jobs near you
Infographic showing various Document Control Associate job openings in Dublin, OH as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 18% Part Time, 2% Contract, and 1% Nights. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $53,077 per year, or $25.5 per hour.

Quality Control Microbiology Technician

STAQ Pharma Inc

Columbus, OH • On-site

$26/hr

Full-time

Posted 29 days ago

Job description


Job Summary:

Quality Control Microbiology Technician 1 will provide clean room support for batch production and ensuring procedure adherence during filling of product. Utilize appropriate controlled documents and assist in quality control deviations/investigations.

Responsibilities:

  • Ensure clean rooms and associated areas meet the required cleanliness standards as per company procedures.
  • Adhere to strict gowning and personal hygiene practices to prevent contamination and maintain integrity of the clean room environment.
    • Perform gowning qualification training for individuals from all departments who must enter ISO 7 classified areas.
  • Monitor and maintain clean room equipment such as viable and non-viable samplers to ensure optimal performance and compliance with established standards.
    • Perform and lead routine environmental monitoring activity in ISO 7 Classified Areas
  • Work with production to resolve Quality issues and ensure documentation is complete.
  • Perform routine and non-routine viable, non-viable and surface environmental monitoring in all classified areas of the facility.
  • Incubation and enumeration of samples related to environmental monitoring processes.
    • Train new personnel on enumeration activities
  • Evaluate organisms by colony morphology and perform subculturing.
    • Train new personnel on colony morphology assessment and subculturing activities.
  • Perform and/or verify gram stain testing morphology results.
  • Continuous improvement activities for environmental monitoring program.
  • Provide quality control and microbiology support for operations.
  • Collect, submit and manage microbiological samples to third party testing laboratories.
  • Assist with QC Microbiologists (and other investigators) with investigations as they relate to environmental monitoring or other quality control deviations.
  • Assist QC Microbiologists with data trending and data reporting as they relate to environmental monitoring or other data-generating processes.
  • Perform routine testing or cleaning associated with the BioSafety Cabinet.
    • Lead and train new personnel on the cleaning procedures and testing procedures carried out in the BioSafety Cabinet
  • Assist in process, procedural, equipment issues via experimentation or revision of procedures.
  • Other duties as assigned.

Required Skills/Abilities: (examples)

  • Experience with cGMP aseptic manufacturing environment.
  • Strong attention to detail.
  • Comfortable in a fast-paced, small company environment and able to adjust workload based upon changing priorities.
  • Preferred previous pharmaceutical experience.
  • Proficient in using Microsoft Word, Excel, PowerPoint, Outlook.
  • Familiarity with 21 CFR Part 11/210/211

Education and Experience:

  • Associate or Bachelor’s degree in Microbiology, Biology, or related life sciences.
  • Experience in microbiology or quality control preferred.
  • Experience in a cGMP or cleanroom setting preferred.

Physical Requirements:

  • Prolonged periods of sitting at a desk or laboratory bench and working on a computer.
  • Must be able to lift up to 15 pounds at times.

The application window for this position is anticipated to be open at least 25 days