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Document Control Associate Jobs in Elk Grove, CA

TekWissen LLC

QC Laboratory Associate

Vacaville, CA · On-site

$20 - $25/hr

Job Title: QC Associate I / QC Laboratory Associate Location: Vacaville, CA - 95688 Duration: 12 ... Core duties include execution of laboratory testing, trend analysis, documentation review ...

Lonza

Quality Control Associate I

Vacaville, CA · On-site

$63K - $106K/yr

Join Lonza in Vacaville, CA as a Quality Control(QC) Associate I. You will be a team member of the ... Identify and document deviations from accepted practices and participate in the evaluation and ...

Sunrise Systems Inc

Be Seen First

Document Specialist_26-04343

West Sacramento, CA · On-site

$19 - $20/hr

Associates degree OR a high school diploma and a minimum of 2 years experience in a document control/administrative role. * Self-starter with the ability to learn quickly and require minimal ...

Accurate Personnel LLC

Quality Control

Roseville, CA · On-site

$20/hr

HIRING IMMEDIATELY: QUALITY CONTROL ASSOCIATE IN ROSEVILLE, CA Accurate Personnel is hiring ... Verify products meet company quality standards * Assist with inventory checks and documentation

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

... documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. * In conjunction with Quality Control leadership, the QC Associate II works to meet ...

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

... C Associate I, is responsible for the performance of direct materials testing in accordance with cGMP regulations. These duties include execution of laboratory testing, trend analysis, documentation ...

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

... documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. * In conjunction with Quality Control leadership, the QC Associate II works to meet ...

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

... documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. * In conjunction with Quality Control leadership, the QC Associate II works to meet ...

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

... documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. * In conjunction with Quality Control leadership, the QC Associate II works to meet ...

Unicon Pharma Inc.

QC Analyst II

Vacaville, CA · On-site

$27.25 - $36.50/hr

... C Associate II, is responsible for the performance of direct materials testing in accordance with cGMP regulations. These duties include execution of laboratory testing, trend analysis, documentation ...

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

... documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. * In conjunction with Quality Control leadership, the QC Associate II works to meet ...

TekWissen LLC

Quality Control Scientist

Vacaville, CA · On-site

$20 - $25/hr

Job Title: QC Associate I / Quality Control Scientist Location: Vacaville, CA - 95688 Duration: 6 ... Write protocols, reports, and technical documentation under limited supervision * Provide and ...

TekWissen LLC

Quality Control Analyst

Vacaville, CA · On-site

$20 - $25/hr

Job Title: QC Associate / Quality Control Analyst I Location: Vacaville, CA - 95688 Duration: 6 ... Write protocols, reports, and technical documentation under limited supervision * Provide and ...

Varsitybrands

QC/Pack/Ship, 2nd Shift

Sacramento, CA · On-site

$18.80/hr

... Shipping Warehouse Associate, ensure products are stocked, selected, packed, and shipped to ... Read and comprehend documents, instructions, and correspondence in English to perform job duties ...

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All JobsDocument Control Associate JobsDocument Control Associate Jobs in Elk Grove, CA

Document Control Associate information

See Elk Grove, CA salary details

$11

$27

$48

How much do document control associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for document control associate in Elk Grove, CA is $27.84, according to ZipRecruiter salary data. Most workers in this role earn between $19.47 and $35.38 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 Elk Grove, CA?

The most popular types of Document Control jobs in Elk Grove, CA are:

What cities near Elk Grove, CA are hiring for Document Control Associate jobs?

Cities near Elk Grove, CA with the most Document Control Associate job openings:

Document Control Associate jobs near you
Infographic showing various Document Control Associate job openings in Elk Grove, CA as of August 2026, with employment types broken down into 82% Full Time, 6% Part Time, 9% Contract, and 3% Nights. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $57,914 per year, or $27.8 per hour.

QC Laboratory Associate

TekWissen LLC

Vacaville, CA • On-site

$20 - $25/hr

Contractor

Re-posted 26 days ago

Job description

Overview:  
  
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.   Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.  
  
Job Title:     QC Associate I / QC Laboratory Associate
Location:     Vacaville, CA - 95688
Duration:     12 Months    
Job Type:    Temporary Assignment 
Work Type: Onsite
 
 
Summary
 
With limited supervision, the QC Associate I is responsible for performing direct materials testing in compliance with cGMP regulations. Core duties include execution of laboratory testing, trend analysis, documentation review, discrepancy support (OOS, OOT, OOE), and general laboratory support activities. In collaboration with QC leadership, the QC Associate II contributes to achieving departmental and organizational objectives.
 
Responsibilities
  • Perform a broad variety of basic and moderately complex tests with documentation according to GMP
  • Review data and assess against established acceptance criteria
  • Perform technical review of peer-generated data
  • Evaluate data to identify trends and/or establish limits
  • Identify discrepancies; provide input to design of quality investigations and CAPA (corrective actions preventive actions) initiatives as needed
  • Identify and troubleshoot technical problems
  • Identify gaps in systems and procedures
  • Receive and provide training
  • Participate in assay transfer and assay validation
  • Perform equipment qualification / maintenance
  • Prepare and maintain standards, controls, stocks, cultures, etc. per established procedures
  • Support the maintenance and compliance of operational areas
  • Assure and apply GMP throughout operations
  • Coordinate with customers to support multi-site operational activities
  • Support internal and external audits and regulatory inspections
  • Works to meet schedules, timelines, deadlines
  • Participate in and/or lead group and project teamwork; project and process improvements
  • Write protocols and reports under limited supervision
  • Meets scheduled performance of 95% on time
  • Perform other duties as requested by managers to support Quality activities.
Required Skills
  • B.S./B.A. degree and 1-3 years experience or Master’s Degree plus one year experience or an equivalent combination of education and experience.
  • Degrees are preferably in relevant scientific disciplines and experience is in the pharmaceutical or biopharmaceutical industry.
  • Strong verbal and written communication skills, ability to organize and present information both formally and informally.
  • Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures.
  • Routinely exercises sound judgment, reasoning and problem solving.
  • Capable of working under limited supervision and determining own short term priorities.
TekWissen® Group is an equal opportunity employer supporting workforce diversity.

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 

TekWissen logo

About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

Social media

Twitter

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