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Document Control Associate Jobs in Chandler, AZ (NOW HIRING)

DPR Construction

Quality Engineer

Phoenix, AZ · On-site

$71K - $92K/yr

... documentation. • Support internal audits, document control, calibration records, quality ... Education and Experience • Associate degree, technical certification, bachelor's degree, or ...

DPR Construction

Quality Engineer

Phoenix, AZ · On-site

$71K - $92K/yr

Support control of nonconforming materials and products, including containment, documentation ... Education and Experience Associate degree, technical certification, bachelor's degree, or ...

DHL

Quality Assurance Supervisor

Goodyear, AZ · On-site

$55K - $90K/yr

... document control, and standard operating procedures/work instructions. * Provide support on key ... Supervise, coach, and train hourly associates supporting quality assurance and control activities ...

DHL

Training Supervisor

Goodyear, AZ · On-site

... for associates and ensure all processes are documented to meet company, regulatory, ISO and ... document control standards are in place and maintained to support ISO and Management of Change ...

HelloFresh

Inventory Control Analyst

Goodyear, AZ · On-site

$58K - $63K/yr

Document findings and contribute to root cause analysis on recurring discrepancies * Maintain ... Associate's or Bachelor's degree in Business, Supply Chain, or a related field preferred You'll get.

DPDHL

Quality Assurance Supervisor

Goodyear, AZ

$55K - $90K/yr

... document control, and standard operating procedures/work instructions. * Provide support on key ... Supervise, coach, and train hourly associates supporting quality assurance and control activities ...

DHL

Quality Assurance Supervisor

Goodyear, AZ · On-site

$55K - $90K/yr

... document control, and standard operating procedures/work instructions. * Provide support on key ... Supervise, coach, and train hourly associates supporting quality assurance and control activities ...

HelloFresh

Inventory Control Analyst

Goodyear, AZ · On-site

Document findings and contribute to root cause analysis on recurring discrepancies * Maintain ... Associate's or Bachelor's degree in Business, Supply Chain, or a related field preferred You'll get.

DPDHL

Quality Assurance Supervisor

Goodyear, AZ · On-site

$55K - $90K/yr

... document control, and standard operating procedures/work instructions. * Provide support on key ... Supervise, coach, and train hourly associates supporting quality assurance and control activities ...

Clearway Energy

Senior Associate, Procurement

Scottsdale, AZ · Hybrid

$95K - $129K/yr

What The Role Is The Senior Associate, Procurement is responsible for supporting the procurement ... document control What Would Be Nice * Experience procuring high-voltage equipment, including ...

Shamrock

Quality Control Technician

Phoenix, AZ · On-site

$18 - $23/hr

Reviews HACCP documents prior to handing paperwork to QA Supervisor/Manager. * Work with ... At Shamrock Foods Company, people come first - our associates, our customers, and the families we ...

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All JobsDocument Control Associate JobsDocument Control Associate Jobs in Chandler, AZ

Document Control Associate information

See Chandler, AZ salary details

$11

$27

$47

How much do document control associate jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for document control associate in Chandler, AZ is $27.04, according to ZipRecruiter salary data. Most workers in this role earn between $18.89 and $34.38 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 Chandler, AZ?

The most popular types of Document Control jobs in Chandler, AZ are:

What cities near Chandler, AZ are hiring for Document Control Associate jobs?

Cities near Chandler, AZ with the most Document Control Associate job openings:

Document Control Associate jobs near you
Infographic showing various Document Control Associate job openings in Chandler, AZ as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 18% Part Time, 3% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $56,251 per year, or $27 per hour.

Clinical Research, Internal Quality Assurance Associate

Castle Biosciences, Inc

Phoenix, AZ

Full-time

Medical, Retirement, PTO

Re-posted 13 days ago

Job description

Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood!

Learn more at www.CastleBiosciences.com

Castle Biosciences Inc. is growing, and we are looking to hire a full-time Clinical Research, Internal Quality Assurance Associate working from our Phoenix, AZ office location, with a start date of September 15, 2026.

Why Castle Biosciences?

Exceptional Benefits Package:

  • Excellent Annual Salary + 20% Bonus Potential
  • 20 Accrued PTO Days Annually + 10 Paid Holidays
  • 401K with 100% Company Match up to 6%
  • 3 Health Care Plan Options + Company HSA Contribution
  • Company Stock Grant Upon Hire

A DAY IN THE LIFE OF AN Internal Quality Assurance Associate

The Internal Quality Assurance Associate supports the day-to-day quality assurance operations of the Clinical Research Department by assisting with the implementation and continuous improvement of the Quality Management System (QMS). This role collaborates with Clinical Research, Quality, and Training teams to support quality initiatives, develop and maintain Standard Operating Procedures (SOPs) and controlled documents, manage document control and Learning Management System (LMS) processes, and assist with internal and external audits and regulatory inspections. The associate ensures compliance with CSTL policies, Good Clinical Practice (GCP), and applicable regulatory requirements while promoting quality, supporting staff training, and maintaining the integrity of clinical research activities and human subject protections.

REQUIRED QUALIFICATIONS

  • Associate degree in related field.
  • Minimum of 2 years of proven experience in clinical quality assurance, training, compliance, regulatory, or a related role.
  • A minimum of 2 years in clinical research.
  • Fundamental understanding of medical/therapeutic area knowledge and medical terminology.
  • Highly skilled in Microsoft Office, proficiency in Microsoft Word and Excel, and the ability to learn appropriate software.

PREFERRED QUALIFICATIONS

  • Bachelor's degree in related field or demonstrated experience as evidence of competency.
  • Previous experience with complex, global trials.
  • Competent in study development processes, current industry standards, such as, but not limited to: ICH GCP, ISO 14155, IDE requirements, HIPAA, GDPR guidelines, Quality Management Systems, and 21 CFR Part 11 guidelines.

*Please see the full job description at the end of the job ad.

SCHEDULE

  • Monday-Friday, 40 hours per week, exempt position, working from our Phoenix, AZ office location.

READY TO JOIN OUR BIOTECH TEAM?

We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon!

Castle Biosciences Awards and Research Developments!

WORK AUTHORIZATION

All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas.

ABOUT CASTLE BIOSCIENCES INC.

At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes.

Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development.

Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities.

If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail ReasonableAccommodationsRequest@castlebiosciences.com.

This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response.

** No third-party recruiters, please

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