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Document Control Associate Jobs in Cleveland, OH

Astrix Inc

QC Associate Scientist

Concord, OH · On-site

$75K - $80K/yr

... skilled QC Associate Scientist to join their team in Lake County, OH! Location: Lake County, OH ... Review analytical data for technical accuracy and adherence to good documentation practices.

Astrix Inc

QC Associate Scientist

Concord, OH · On-site

We're hiring an Associate Scientist with analytical experience to join a global leader in the ... Investigate out-of-specification (OOS) results and document findings * Ensure timely and compliant ...

Astrix Inc

QC Associate Scientist

Concord, OH · On-site

Investigate out-of-specification (OOS) results and document findings * Ensure timely and compliant ... Strong working knowledge of GLP/GMP standards, quality control procedures, and laboratory ...

Piping Rock

Inventory Associate II 2nd Shift

Mantua, OH · On-site

$26 - $28.60/hr

Under the direction of the Manager/Supervisor/Lead Person, the Inventory Control Associate II is ... Must comply with GMP requirements; specific functions and documents will be discussed in GMP and on ...

Piping Rock

Inventory Associate II 1st Shift

Mantua, OH · On-site

$26/hr

Under the direction of the Manager/Supervisor/Lead Person, the Inventory Control Associate II is ... Must comply with GMP requirements; specific functions and documents will be discussed in GMP and on ...

Adecco

Quality Control Technician

Walton Hills, OH · On-site

$20 - $21/hr

Count and document production materials * Maintain clean and organized work area * Assist on ... Pay Details: $20.00 to $21.00 per hour Benefit offerings available for our associates include ...

Adecco

Quality Control Technician

Walton Hills, OH · On-site

$20 - $21/hr

Count and document production materials * Maintain clean and organized work area * Assist on ... Pay Details: $20.00 to $21.00 per hour Benefit offerings available for our associates include ...

W3Global Inc.

Manufacturing Engineer

Mentor, OH

$85K - $95K/yr

Update and maintain drawing revisions and document control within the CAD/PDM system. * Assist in ... Associate degree or technical diploma in Mechanical Design, Drafting Technology, or related field ...

Vogelsang

Control Panel Technician

Ravenna, OH · On-site

$17.25 - $22.25/hr

Document service activities and communicate effectively with customers and internal teams ... Associate degree in a technical field, military experience, or equivalent work experience. * Strong ...

Vogelsang

Control Panel Technician

Ravenna, OH · On-site

$17.25 - $22.25/hr

Document service activities and communicate effectively with customers and internal teams ... Associate degree in a technical field, military experience, or equivalent work experience. * Strong ...

Vogelsang

Control Panel Technician

Ravenna, OH

$17.25 - $22.25/hr

Document service activities and communicate effectively with customers and internal teams ... Associate degree in a technical field, military experience, or equivalent work experience. * Strong ...

Avtron Power Solutions, LLC

Drafter

Cleveland, OH · On-site

Maintain drawing revision control in accordance with Avtron document control processes MINIMUM ... Education: * BS in Engineering or Computer Aided Design (CAD) preferred, Associate Degree in ...

Harris Company

Administrative Assistant

Brook Park, OH

$17 - $22.75/hr

... to reporting, document control, and maintaining important company records. You'll work with ... Associate degree preferred 2+ years of administrative or office support experience preferred Strong ...

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All JobsDocument Control Associate JobsDocument Control Associate Jobs in Cleveland, OH

Document Control Associate information

See Cleveland, OH salary details

$10

$25

$44

How much do document control associate jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for document control associate in Cleveland, OH is $25.69, according to ZipRecruiter salary data. Most workers in this role earn between $17.93 and $32.64 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 are the most commonly searched types of Document Control jobs in Cleveland, OH?

The most popular types of Document Control jobs in Cleveland, OH are:

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

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

Document Control Associate jobs near you
Infographic showing various Document Control Associate job openings in Cleveland, OH as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 19% Part Time, 4% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $53,428 per year, or $25.7 per hour.

QC Associate Scientist

Astrix Inc

Concord, OH • On-site

$75K - $80K/yr

Full-time

Re-posted 21 days ago

Job description

Our client, a leading contract manufacturer and research organization of API's, is looking for a skilled QC Associate Scientist to join their team in Lake County, OH!
Location: Lake County, OH
Salary: $75,000 - $80,000 per year
Employment Type: Full-time
Position Summary
The QC Associate Scientist will support a GMP-regulated API analytical laboratory by performing routine and non-routine analytical testing, method transfers, and investigations. This role requires strong expertise in HPLC and GC analysis, experience working within cGMP environments, and the ability to collaborate cross-functionally to support project timelines and quality objectives.
Responsibilities
  • Perform routine HPLC and GC analyses in a GMP API analytical laboratory.
  • Execute and support GMP analytical method transfers, including preparation of transfer protocols and final reports.
  • Conduct additional analytical techniques as needed, including but not limited to: FTIR, IC, Karl Fischer (KF), XRD, NMR, DSC, TGA, particle size analysis, Titrations, UV-Vis spectroscopy, and optical rotation.
  • Coordinate release testing for raw materials, intermediates, and active pharmaceutical ingredients (APIs).
  • Perform out-of-specification (OOS) investigations and support root cause analysis.
  • Ensure timely and compliant generation of analytical data to meet project and regulatory timelines.
  • Review analytical data for technical accuracy and adherence to good documentation practices.
  • Maintain compliance with cGMP, GLP, and laboratory safety requirements.
  • Collaborate effectively with Quality Assurance, Production, and Technical teams.
  • Perform other duties as assigned.

Qualifications
  • Bachelor's degree (B.S.) in Chemistry or related scientific discipline required.
  • Minimum of 5 years of experience in a pharmaceutical analytical laboratory or equivalent combination of Strong hands-on experience with HPLC and GC instrumentation.
  • Proficient with standard laboratory equipment (balances, pipettes, pH meters, etc.).
  • Solid understanding of analytical chemistry principles and laboratory safety practices.
  • education and experience.
  • Demonstrated experience working in cGMP/GLP environments, including QC or stability testing.
  • Experience interacting with Quality Assurance and regulatory documentation.

*This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! *
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