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

Associate's degree in relevant field and 3 years of relevant experience, or * In lieu of degree, 5 years project controls, document control, and/or technical administrative support experience What ...

Communicate with Leadership in each department pertaining to Associate errors * Communicate with Merchandise Control team on errors that may be impacting items in reserve locations * Update accuracy ...

Communicate with Leadership in each department pertaining to Associate errors * Communicate with Merchandise Control team on errors that may be impacting items in reserve locations * Update accuracy ...

Communicate with Leadership in each department pertaining to Associate errors * Communicate with Merchandise Control team on errors that may be impacting items in reserve locations * Update accuracy ...

Track documentation status and turnaround times to prevent project delays. * Maintain audit-ready ... Associate's or Bachelor's in Engineering/Technology preferred. * NETA Level I/II, ASQ CQA, or ...

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Document Control Associate information

See Columbus, OH salary details

$10

$25

$44

How much do document control associate jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for document control associate in Columbus, OH is $25.58, according to ZipRecruiter salary data. Most workers in this role earn between $17.88 and $32.50 per hour, depending on experience, location, and employer.

What jobs make $3,000 a month without a degree?

A Document Control Associate typically earns less than $3,000 per month, but roles such as administrative assistants, sales representatives, or certain skilled trades like HVAC technicians can earn around or above this amount without a college degree. Success in these roles often depends on experience, certifications, or on-the-job training rather than formal education.

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

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.

What are Document Control Associates?

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 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.

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 are the most commonly searched types of Document Control jobs in Columbus, OH? The most popular types of Document Control jobs in Columbus, OH are:
What cities near Columbus, OH are hiring for Document Control Associate jobs? Cities near Columbus, OH with the most Document Control Associate job openings:
Document Control Specialist I

Document Control Specialist I

Forge Biologics

Columbus, OH

Other

Medical, Dental, Vision, Retirement, PTO

Posted 10 days ago


Job description

Forge Your Future with Us: 

At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is simple yet powerful: to enable access to life-changing gene therapies and help bring them from ideas into reality. We partner with scientists, physicians, biotech and pharma innovators, and patient communities - all united by one goal: improving lives. If you're driven by purpose and excited to make a tangible impact, this is where your journey begins. 

Our team works out of The Hearth, a state-of-the-art, 200,000-square-foot cGMP facility in Columbus, Ohio. Here, you won't just watch innovation happen - you'll be part of it. Whether you're scaling AAV manufacturing, collaborating on cutting-edge therapies, or supporting complex technical projects, you'll play a key role in bringing hope to patients with genetic diseases. 

What sets Forge apart is our culture of H.O.P.E. We are hardworking, showing up each day with determination and grit. We are open, creating a space where ideas flow freely and every voice is valued. We are purpose-driven, with every task directly tied to changing lives. And we are engaged, energized by the challenges we face and the milestones we achieve together. 

At Forge, your growth matters. We're committed to helping you expand your skills, take on new challenges, and develop your career through mentorship, hands-on learning, and opportunities for advancement. Our people are our greatest investment, and we're proud to see team members grow with us. 

If you're ready to use your talent to help deliver hope to patients around the world, join us - and be part of something bigger than yourself. 

About The Role:   

The Document Control Specialist I, Quality Assurance plays a pivotal role in ensuring regulatory compliance and seamless operation of the document management system utilizing an Electronic Quality Management System. This position is responsible for overseeing Document Control and Records Management functions, with a focus on maintaining GxP standards. 

Responsibilities: 

  • Issue controlled documents, including batch records, labeling, forms, and logbooks, to Operations and Quality Control departments, ensuring they are accurate, complete, and compliant. 
  • Collaborate with cross-functional teams to streamline document issuance and reconciliation processes across departments. 
  • Reconcile and review completed GMP documentation records for accuracy and completeness. 
  • Serve as a subject matter expert for the document management system (eQMS/Veeva Vault) and provide guidance on document authoring and revision. 
  • Scan and process executed batch records and other GMP documentation into the eQMS in a timely and efficient manner. 
  • Support the creation and reporting of metrics and internal KPIs related to the document management system. 
  • Identify and implement process improvements that strengthen document control and support compliance with internal and regulatory requirements. 
  • Support regulatory inspections and internal audits by ensuring documentation is organized, complete, and inspection-ready. 

Qualifications: 

  • High school diploma or equivalent (GED). 
  • Intermediate proficiency in Microsoft Office applications (Outlook, Teams, Word, Excel, and Powerpoint). 
  • Proven track record of keen attention to detail, consistently ensuring accuracy and precision in all tasks and documentation. 
  • Strong communication skills, both written and verbal. 

Preferred Skills: 

  • Associate's or Bachelor's Degree. 
  • Basic proficiency with Project Management software (Smartsheet). 
  • Advanced proficiency with Microsoft Office applications (Outlook, Teams, Word, Excel, and Powerpoint). 
  • Experience in Document Control, Records Management, or Quality Assurance within a GMP environment. 
  • Experience with eQMS, preferably Veeva Vault or another document management system. 

This position works in a typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. This islargely asedentary role; persons holding office positions aregenerally subjectto inside environmental conditions having the lighting, temperature, and noise of an open floor-plan office environment. Regularlyoperatea computer and other office equipment. Regularly communicate with others in person, over the phone, and electronically. Must be able to move and/or carry objects weighing up to 10 lbs. 

Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce.Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. 

We've Got You Covered:  

At Forge Biologics, we believe our people deserve to be taken care of - in and out of the workplace. We've built a comprehensive compensation and benefits package designed to help you thrive, grow, and feel valued every step of the way:  

Health from day one 

  • Health, dental and vision insurance start your first day - with 90% of premiums covered for you and your family.  

Time to recharge 

  • A competitive paid time off plan - because rest fuels innovation.  
  • 12 weeks of fully paid parental leave so you can focus on family when it matters most.  

Rewarding your impact 

  • Annual bonus opportunities for all full-time team members.  
  • 401(k) with company match to help you plan for the future.  
  • Special employee discounts, including childcare and dependent care savings.  

Your wellness, supported 

  • Onsite fitness facility at The Hearth. 
  • Mental health counseling and financial planning services through our Employee Assistance Program.  
  • Employer-paid short and long-term disability coverage to protect your peace of mind.  

Fuel for your workday 

  • A fully stocked kitchen with free snacks and beverages - we keep you energized and ready for what's next.  

Grow with us 

  • Ongoing professional development resources, training, and mentorship programs to help you build your care and grow within Forge. Â