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Laboratory Document Control Jobs (NOW HIRING)

Laboratory notebooks * Production and laboratory logbooks * Quality Receiving paperwork * Maintain document/file room processes, including filing of documents * Complete documents verification ...

Laboratory notebooks * Production and laboratory logbooks * Quality Receiving paperwork * Maintain document/file room processes, including filing of documents * Complete documents verification ...

... control, Gmp, Data entry, Batch record, Quality assurance, Sop, Batch record review, Microsoft ... in a laboratory science Be able to handle all documents and follow SOPs Experience Level ...

We are currently seeking a Quality Control Document Specialist with a strong background in ... Minimum of 1 year of experience in a microbiology laboratory within a cGMP-regulated manufacturing ...

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Laboratory Document Control information

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$14

$27

$52

How much do laboratory document control jobs pay per hour?

As of Jun 5, 2026, the average hourly pay for laboratory document control in the United States is $27.84, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $31.97 per hour, depending on experience, location, and employer.

How does the Laboratory Document Control role interact with laboratory staff and management on a daily basis?

In the Laboratory Document Control role, you will regularly collaborate with both laboratory staff and management to ensure all documentation, such as SOPs, protocols, and reports, are current, accurate, and compliant with regulatory standards. Your daily responsibilities often include coordinating document reviews, managing revision histories, and distributing updated documents to relevant teams. Clear communication and organizational skills are essential, as you will serve as a bridge between technical staff and quality assurance to support smooth lab operations and audit readiness.

What is Laboratory Document Control?

Laboratory Document Control refers to the management of documents related to laboratory operations, such as standard operating procedures (SOPs), test methods, quality manuals, and records. Document control specialists ensure that all documents are accurate, up-to-date, and accessible to authorized personnel while maintaining compliance with regulatory standards. This role often involves organizing, reviewing, updating, and archiving documents, as well as training staff on document control procedures. Effective document control helps maintain quality, traceability, and accountability in laboratory environments.

What is the difference between Laboratory Document Control vs Laboratory Technician?

AspectLaboratory Document ControlLaboratory Technician
Primary RoleManaging and maintaining laboratory documentation, ensuring compliance and accuracyPerforming tests, recording data, and supporting laboratory operations
Required CredentialsTypically certifications in document management or quality assurance, sometimes a relevant degreeAssociate or bachelor's degree in science or related field
Work EnvironmentOffice or laboratory setting focused on documentation and complianceHands-on laboratory environment performing experiments and tests
Industry UsageUsed across regulated industries like pharmaceuticals, biotech, and manufacturingCommonly employed in laboratories for testing and analysis

Laboratory Document Control focuses on managing laboratory records and ensuring compliance, while Laboratory Technicians perform testing and data collection. Both roles are essential in laboratory operations but serve different functions within the industry.

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

To thrive as a Laboratory Document Control specialist, you need meticulous attention to detail, organizational skills, and familiarity with quality management standards, often backed by a degree in science or a related field. Proficiency with document management systems (DMS), electronic laboratory notebooks (ELN), and regulatory compliance tools such as ISO 17025 or GLP is typically required. Strong communication, time management, and problem-solving abilities help ensure accuracy and efficient collaboration across departments. These skills and qualities are crucial for maintaining data integrity, regulatory compliance, and smooth laboratory operations.
Infographic showing various Laboratory Document Control job openings in the United States as of May 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $57,910 per year, or $27.8 per hour.
Intern - Document Control

Intern - Document Control

Tolmar

Fort Collins, CO โ€ข On-site, Remote

$19/hr

Full-time

Medical, Retirement

Posted 7 days ago


Job description

ย 

About Tolmar

Tolmar is a fully integrated pharmaceutical company based in Colorado that develops, manufactures, and globally distributes branded and generic prescription pharmaceuticals in the areas of urology and oncology. Tolmar is a leader in the development and manufacturing of specialty injectable products such as ELIGARDยฎ, FENSOLVIยฎ and oral class Jatenzo.

Passion guides our commitment to providing the highest level of support to the health care providers and patients within the disease states that our products treat. Our highly experienced commercial leadership team are dedicated to advancing our pipeline of products and expanding our portfolio to serve important patient medical needs.

Interested in exploring Tolmarโ€™s commitment to our patience and our personnel, then please join us to launch your career.

About Document Control

1. Purpose and Scope

Document Control supports Tolmar by establishing, processing and maintaining governance documents that drive consistent use throughout the organization, processing controlled documents and maintaining the Document Control system.

2. Essential Duties & Responsibilities

  • Update and maintain associated tracking systems including:
    • Lab notebook issuance and archival
  • Support team document true copy reviews and document retention schedules as necessary.
  • Scanning files and other documents/records ensuring proper retention requirements including:
    • Department document submissions
    • Laboratory notebooks
    • Production and laboratory logbooks
    • Quality Receiving paperwork
    • Maintain document/file room processes, including filing of documents
  • Complete documents verification requirements for scanned documents.
  • Support departments as necessary with required tasks supported.
  • Ensure open communication as needed when discrepancies/errors are found.
  • Other duties as assigned.

Knowledge, Skills & Abilities

  • Knowledge of Microsoft Word and Excel.
  • Use of a flat scanner, preferred
  • Knowledgeable of FDA and other regulatory Good manufacturing Practices (cGMP).
  • Excellent organizational skills.
  • Ability to maintain focus on detail-oriented, repetitive tasks.
  • Effective verbal and written communication to support broad range of departments.
  • Ability to interact with team members and other departments in a respectful and professional manner.
  • Veeva experience is preferred but not required.

Core Values

The Intern is expected to operate within the framework of Tolmarโ€™s Core Values:

  • Center on People: We commit to support the well-being of our patients and treat our employees and those we serve as valued partners. By placing people at the heart of our actions, we actively engage, invigorate, acquire knowledge, and grow together with an enterprise-wide mindset that lifts the whole organization.
  • Are Proactive & Agile: We embody a culture of engagement and action. With a hands-on approach, we fearlessly adapt to change. We anticipate, respond swiftly and efficiently to ignite a spirit that propels us towards extraordinary outcomes.
  • Act Ethically: We are committed to consistently conducting our business in an ethical, compliant, and socially aware manner, in line with our purpose of positively impacting lives. We actively cultivate diversity, equity, inclusion & sustainability in our workplace.
  • Constantly Improve: We are committed to a proactive, collaborative effort to enhance our products, systems, processes, and services by reducing waste, increasing efficiency, and improving quality.
  • Are Accountable: We think, act, and communicate with honesty, transparency, and clarity in alignment with our core values. We don't compromise our values for near term gain. We take accountability & ownership of our work, actions, successes, and setbacks. We strive to deliver our best as we shape the future.

Education & Experience

  • Enrolled full-time and pursuing an undergraduate or graduate degree in pharmaceuticals or closely related program.
  • Have achieved an overall cumulative GPA of 3.0 (on a 4.0 scale) or higher.

Working Conditions

  • Working conditions are normal for an office environment.
  • Work will be on-site in both Fort Collins and Windsor. Some work may be performed remotely.
  • The intern must have access to a private, quiet working area during business hours (8 AM-5 PM Mountain Time).

Compensation and Benefitsย 

  • Pay: $19.00 per hourย 
  • Benefits include medical insurance and 401k participationย 
  • Benefits summary: https://www.tolmar.com/careers/employee-benefits

Tolmar compensation programs are focused on equitable, fair pay practices including market-based base pay and a strong benefits package. The final compensation offered may vary from the posted range based on the selected candidate's qualifications and experience.ย 

Tolmar is an Equal Opportunity Employer. We do not discriminate on the basis age 40 and over, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation or any other applicable status protected by state or local law. It is our intention that all qualified applicants be given equal opportunity and that selection decisions are based on job-related factorsย 


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About Tolmar

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Fort Collins, CO, US

Year founded

2006