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Document Control Associate Jobs in South Dakota (NOW HIRING)

Office Coordinator

Sioux Falls, SD · On-site

$18 - $24/hr

Provide backup to Document Control Specialist Quality/Engineering * Prepare regularly scheduled ... Associate degree in office administration or related field preferred. * Physical Requirements:

... to document structural, sanitation, and pest issues Deliver timely, cost-effective, and high ... Building on a century of innovation, our 48,000 associates help deliver comprehensive science-based ...

Use handheld computerized equipment to document structural, sanitation, and pest issues * Deliver ... Building on a century of innovation, our 48,000 associates help deliver comprehensive science-based ...

Use handheld computerized equipment to document structural, sanitation, and pest issues * Deliver ... Building on a century of innovation, our 48,000 associates help deliver comprehensive science-based ...

Use handheld computerized equipment to document structural, sanitation, and pest issues * Deliver ... Building on a century of innovation, our 48,000 associates help deliver comprehensive science-based ...

Use handheld computerized equipment to document structural, sanitation, and pest issues * Deliver ... Building on a century of innovation, our 48,000 associates help deliver comprehensive science-based ...

Perform audit testing, walkthroughs, substantive procedures, and internal control evaluations ... Analyze financial records and supporting documentation * Assist with the preparation of financial ...

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Document Control Associate information

See South Dakota salary details

$11

$26

$46

How much do document control associate jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for document control associate in South Dakota is $26.49, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $33.65 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 South Dakota? The most popular types of Document Control jobs in South Dakota are:
What are popular job titles related to Document Control Associate jobs in SD? For Document Control Associate jobs in SD, the most frequently searched job titles are:
Infographic showing various Document Control Associate job openings in South Dakota 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 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $55,090 per year, or $26.5 per hour.

Associate Quality & Compliance Manager

Electronic Systems Sioux Falls

Sioux Falls, SD

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

New


Job description

HELP BUILD QUALITY INTO EVERYTHING WE DO.

ASSOCIATE QUALITY & COMPLIANCE MANAGER | DAY SHIFT | MONDAY–FRIDAY

ABOUT ESI

At ESI, we build lasting partnerships with our customers by delivering products Done Right, On Time, backed by Legendary Service. We design, assemble, and deliver complex electronic products that power industries across the globe. Our success is driven by our people, innovators who don’t just solve problems but continuously improve how we work every day.

WHAT YOU’LL DO

As our Associate Quality & Compliance Manager, you’ll help lead the systems, people, and processes that keep quality at the center of how ESI operates. Working alongside our Quality & Compliance Manager and cross-functional leadership, you’ll support the effectiveness and continual improvement of our Quality Management System while helping develop a strong, proactive quality culture.

In this role, you will:

  • Support the administration and continual improvement of ESI’s Quality Management System (QMS), including ISO 9001, ISO 13485, ITAR, and customer-specific requirements.
  • Lead and develop assigned Quality and Service team members through clear expectations, coaching, feedback, and accountability.
  • Coordinate internal audits, CAPA activities, root cause investigations, corrective actions, document control, and Management Review activities.
  • Partner with Operations, Engineering, Materials, and Customer Program Management to improve product quality, first-pass yield, process capability, and manufacturing performance.
  • Identify recurring defects, process variation, and emerging quality risks and help drive effective, sustainable solutions.
  • Support supplier quality activities, including qualification, performance monitoring, corrective actions, and improvement initiatives.
  • Coordinate assigned customer quality investigations, complaints, corrective actions, and quality-related communication.
  • Analyze quality metrics and trends related to scrap, rework, defects, customer complaints, supplier performance, audits, and CAPA effectiveness.
  • Support customer, supplier, registrar, and regulatory audits and ensure findings and commitments are effectively resolved.
  • Champion continuous improvement through data-based decision-making, Lean principles, Statistical Process Control, Six Sigma, and other quality improvement methodologies.

WHAT YOU’LL BRING

  • Bachelor’s degree in Engineering, Manufacturing, Industrial Technology, Operations Management, Business, Quality Management, or a related field, or an equivalent combination of education, training, and relevant experience
  • 5+ years of progressive quality experience in a manufacturing environment
  • 2+ years of supervisory, team-lead, or management experience
  • Experience supporting, maintaining, and improving a Quality Management System
  • Working knowledge of ISO standards, auditing, CAPA, root cause analysis, document control, supplier and customer quality, and continuous improvement
  • Strong leadership, communication, analytical, organizational, and problem-solving skills
  • Ability to interpret customer specifications, technical documentation, procedures, quality standards, and regulatory requirements
  • Ability to manage competing priorities and make sound decisions in a fast-paced manufacturing environment

Even better if you bring:

  • Experience with ISO 9001 and/or ISO 13485
  • Experience with ITAR or other regulated manufacturing requirements
  • Electronics Manufacturing Services (EMS), printed circuit board assembly (PCBA), medical device, or high-mix/low-volume manufacturing experience
  • Experience supporting customer, supplier, internal, or registrar audits
  • Lean Manufacturing, Six Sigma, or Statistical Process Control experience
  • ASQ or other relevant quality certification

PHYSICAL & WORK ENVIRONMENT

This position works across both professional office and electronics manufacturing environments and requires regular interaction with associates, leaders, customers, suppliers, and auditors.

  • Ability to sit, stand, and frequently walk throughout office and manufacturing areas
  • Occasional lifting, carrying, pushing, or pulling up to 25 pounds
  • Frequent computer and standard office equipment use
  • Ability to safely access production, inspection, warehouse, and office areas
  • Exposure to manufacturing equipment, production materials, moderate noise, and electronics manufacturing processes
  • Required use of Personal Protective Equipment (PPE) in designated areas
  • Occasional schedule flexibility and limited travel to support audits, customers, suppliers, training, and business needs

ITAR COMPLIANCE REQUIREMENT

This position requires access to areas, technical data, and/or information subject to the International Traffic in Arms Regulations (ITAR). In accordance with applicable federal requirements, candidates must qualify as a U.S. Person as defined under ITAR, including a U.S. citizen, lawful permanent resident, or other protected individual as defined by applicable law. Verification of eligibility will be required.

WHY ESI

At ESI, we believe in growing our people. We offer career paths built around curiosity, capability, and continuous improvement. Whether it’s leadership development, new certifications, or hands-on training, we’ll help you keep learning and recognize the results you deliver.

For the right quality professional, this role provides the opportunity to expand technical expertise, leadership capability, and business knowledge while preparing for broader quality management responsibilities as ESI continues to grow.

BENEFITS (For Full-Time Employees)

  • Paid Time Off
  • Paid Holidays
  • Three Sanford Health medical options
  • Delta Dental of SD
  • VSP vision
  • Long-Term Disability
  • Voluntary Short-Term Disability
  • AFLAC supplemental plans
  • 401(k) match
  • Company-paid Life/AD&D

EEO & ACCOMMODATIONS

ESI is an equal opportunity employer. Federal law obligates us to provide reasonable accommodation to the known disabilities of applicants and associates, unless doing so would pose an undue hardship. If you require an accommodation to complete the application or interview process, please let us know.


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