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Document Control Associate Jobs in Elk Grove, CA

TERRACON

Project Coordinator - Exploration

Lodi, CA · On-site

Provide project delivery support including document control and administration, project tracking ... Associate or bachelor's degree in related field preferred. * Experience with gINT Geotechnical ...

Trimark Associates

Technical Writer - SCADA

Folsom, CA · Remote

Maintain document revision history and version control throughout the project lifecycle. * Ensure ... Represent the Trimark Associates brand professionally to customers and vendors. * Periodically ...

Trimark Associates

Technical Writer - SCADA

Folsom, CA · Remote

$90K - $115K/yr

Maintain document revision history and version control throughout the project lifecycle. * Ensure ... Represent the Trimark Associates brand professionally to customers and vendors. * Periodically ...

Trimark Associates, Inc

Technical Writer - SCADA

Folsom, CA · On-site

$90K - $115K/yr

Maintain document revision history and version control throughout the project lifecycle. * Ensure ... Represent the Trimark Associates brand professionally to customers and vendors. * Periodically ...

Bowhead

SCA Secretary II

Travis Air Force Base, CA · On-site

Document control - Track, format, and distribute controlled documents such as dig permits, outage ... Associate's degree in Business Administration, Office Management, or a related field. * Years of ...

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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

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$48

How much do document control associate jobs pay per hour?

As of Aug 12, 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 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.

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 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 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 83% Full Time, and 17% Part Time. Highlights an 100% In-person job distribution, with an average salary of $57,914 per year, or $27.8 per hour.

Specialist, Quality Control - Microbiologist (Contract Role)

Orca Bio

Sacramento, CA

$27.25 - $35.75/hr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 days ago

Job description

More than one million people in the United States today are fighting blood cancer. While a traditional allogeneic stem cell transplant has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a commercial-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks. With our purified, high-precision cell therapies we hope to not only replace patients' blood and immune systems with healthy ones, but also restore their lives.
 
We operate a dedicated clinical manufacturing facility in Sacramento, CA (3400 Business Drive), which has historically served as the foundation for producing our high-precision cell therapy products. This site plays a critical role in advancing our clinical pipeline and ensuring the consistent, reliable supply of therapies for patients participating in our trials.

Contractor/Consultant - Quality Control
Location: Sacramento, CA 
Engagement Type: Contract / Consultant 

The Specialist, Quality Control - Microbiologist (Contract) position is a key role in meeting the quality policy through their management of the different quality systems, including production records and deviation system management. The ideal candidate will be responsible for managing the quality systems, including deviations, change control, corrective and preventive actions (CAPA), and document management. Additionally, this role involves making timely batch disposition decisions to ensure quality standards are met before product release, supporting the rapid processing times required by our product. You will have the unique opportunity to make a difference in the lives of many patients as Orca Bio develops next-generation cell therapies.
 
Duration: 
  • Approximately 6 months (July-December)
Physical Demands
  • Production Associates: Must have visual acuity of 20/20 (corrected or uncorrected) and normal color vision to safely perform critical tasks such as visual inspection of materials, equipment, and labeling, including distinguishing color-coded components in a GMP environment.
  • Must be able to meet cleanroom gowning requirements, including wearing full gowning (face coverings, gloves, hoods, goggles) for extended periods, as needed. Use of cosmetics (makeup, painted nails), jewelry, or facial piercings is not permitted in the cleanroom, and any skin conditions that cause shedding must be disclosed.
Work Conditions
  • Must be able to work at either Orca Bio Sacramento location (3400 Business Dr. or 7910 Metro Air Pkwy) based on operational needs.
  • Must be comfortable regularly participating in video-based meetings.
  • May be required to work scheduled overtime, weekends, or holidays based on business needs.
Responsibilities
Quality System Management:
  • Oversee the management of quality systems including deviations, change controls, CAPAs, and document control.
  • Ensure that all deviations are investigated thoroughly and timely, identifying root causes and implementing effective corrective actions.
  • Review and approve change controls to ensure compliance with regulatory requirements and internal procedures.
  • Maintain and improve CAPA processes to ensure effective resolution of quality issues.
Batch Disposition:
  • Evaluate batch records and associated documentation to make informed batch release decisions.
  • Collaborate with manufacturing and quality control teams to ensure all products meet regulatory and quality standards before release.
  • Monitor and document any quality issues related to batch production and implement corrective measures as necessary.
Document Management:
  • Maintain the document management system to ensure all quality-related documents are accurate, current, and compliant with regulatory standards.
  • Conduct regular reviews of quality documentation to ensure adherence to established protocols and procedures.
Regulatory Compliance:
  • Stay informed of current regulations, industry trends, and best practices in pharmaceutical quality assurance.
  • Assist in preparing for internal and external audits, ensuring that all quality systems and documentation are audit-ready.
Training and Support:
  • Provide training and guidance to staff on quality systems, processes, and compliance requirements.
  • Serve as a point of contact for quality-related inquiries and issues, fostering a culture of quality within the organization.
Continuous Improvement:
  • Participate in continuous improvement initiatives to enhance the effectiveness and efficiency of quality systems and processes.
  • Identify areas for improvement within quality operations and suggest appropriate solutions.
  • Track completion of quality records and maintain metrics.
  • Perform other duties as requested by supervisor/manager to support Quality
  • Work collaboratively with cross-functional teams, including manufacturing, research and development, and quality assurance, to support the overall quality of cell therapy products.
General Requirements
  • Communicate effectively with team members and contribute to a positive and collaborative work environment
  • Actively participate in group and project teamwork; project and process improvements
  • Strong organizational skills and the ability to manage multiple tasks concurrently
  • Willingness to learn and adapt in a fast-paced, dynamic environment
  • Adhere to cGMP policies and procedures, including documentation activities
  • Able to wear appropriate personal protective equipment
  • Willingness to work overtime as required
  • Be available to provide on-call support outside regular business hours as needed 
Experienced Required
  • Bachelor's degree in a relevant scientific discipline (biology, biochemistry, immunology, etc.) with 3+ years of experience in quality control testing, analytical development, or GMP; OR a Master's degree in relevant scientific disciplines with 1+ years of experience
  • Understanding of FDA regulations, GMP compliance, and quality system processes
  • Experience in quality control or GMP within a cell therapy or biopharmaceutical manufacturing environment is preferred
  • Able to meet project and testing timelines
  • Detail-oriented with a commitment to data integrity and accuracy, and an ability to identify problems with data management
  • Able to work collaboratively to respond to changing priorities and challenges
  • Ability to work both independently and collaboratively with a multi-disciplinary team in a fast-paced and regulated environment
  • Prior experience doing internal audits and document control management
$35 - $50 an hour
The anticipated annual salary range for this job is based on prior experience in the role/industry, education, location, internal equity, and other job-related factors as permitted by law. For remote-based positions, this range may vary based on your local market. Full-time employment positions will also be eligible to receive pre-IPO equity and annual bonus, in addition to competitive medical, dental, and vision benefits, PTO, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits. Other perks include subsidized daily lunches and snacks at our on-site locations.
 
Who we are
 
We are driven by a passion for science and compassion for patients. We act with urgency to ensure our treatments are one day accessible to all who need them.
 
We live by our core values of passion, courage, and integrity. Excellence in our work means the chance to unlock a better quality of life for our patients, and with that comes tremendous responsibility.
 
We innovate on a path that hasn't been paved. We embrace an entrepreneurial spirit and take calculated risks to achieve our mission. We aren't afraid to ask "why not" and challenge the status quo.
 
We maintain a start-up culture of camaraderie and leadership by example, regardless of title.
 
We're proud to be an equal opportunity employer, and recognize that celebrating our differences creates stronger, lasting solutions that better serve our team, our patients and their healthcare providers.
 
Notice to staffing firms
 
Orca Bio does not accept resumes from staffing agencies with which we do not have a written agreement and specific engagement for a particular opening. Our employment activities, inquiries and offers are managed through our HR/Talent team, and all candidates are presented through this channel only. We do not accept unsolicited resumes, and we rarely outsource recruitment.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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