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Qa Document Control Associate Jobs in Raleigh, NC

Allegiance Staffing

Quality Assurance

Cary, NC

$18.50/hr

Document audit findings and communicate performance gaps or training needs promptly and professionally. * Assist with onboarding and training of temporary QA employees provided through staffing ...

MASTER-PJK SERVICE LLC

QA-Technician-PWP

Raleigh, NC · On-site

$18 - $19/hr

The Production Quality Assurance Technician will complete monitoring warehouse adherence to SOPs ... Record keeping, documentation, and document control experience preferred * Bi-lingual (Spanish ...

Aerogen Ltd

Senior Director of Quality

Morrisville, NC · On-site

... assurance systems and activities. Will provide the signatory authorization from Quality for control documentation and final product disposition. Will be responsible for the investigations and ...

MASTER-PJK SERVICE LLC

QA-Technician-PWP

Raleigh, NC

$18 - $19/hr

The Production Quality Assurance Technician will complete monitoring warehouse adherence to SOPs ... Record keeping, documentation, and document control experience preferred * Bi-lingual (Spanish ...

Cypress Creek Renewables

QA/QC Solar Technician

Raleigh, NC · On-site

$18.25 - $23.25/hr

The Role Cypress Creek Energy is seeking a highly motivated QA/QC Solar Technician with utility ... Generate detailed inspection reports and maintain thorough documentation. * Maintain accurate ...

Focused HR Solutions

8-11 QA Tester

Raleigh, NC · On-site

$35 - $47/hr

Experience in working with the Business Teams to write Business and QA Documents . Required 3 Years ... Local candidates only accepted. Required. By replying to this job advertisement, I agree I want to ...

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All JobsQa Document Control Associate JobsQa Document Control Associate Jobs in Raleigh, NC

Qa Document Control Associate information

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$10

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How much do qa document control associate jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for qa document control associate in Raleigh, NC is $25.75, according to ZipRecruiter salary data. Most workers in this role earn between $17.98 and $32.69 per hour, depending on experience, location, and employer.

What is the difference between Qa Document Control Associate vs Quality Assurance Specialist?

AspectQa Document Control AssociateQuality Assurance Specialist
CredentialsTypically requires a high school diploma or associate degree; certifications like ISO or document control training are commonRequires a bachelor's degree in a related field; certifications such as ASQ CQE or CQA are often preferred
Work EnvironmentOffice and document management settings within manufacturing, pharmaceutical, or biotech industriesQuality labs, manufacturing sites, or office environments focused on product quality and compliance
Employer & Industry UsageUsed by companies needing document control for quality systems in regulated industriesUsed by organizations ensuring product quality, compliance, and process improvements

The Qa Document Control Associate primarily manages and maintains quality documentation, ensuring compliance and proper record keeping. In contrast, the Quality Assurance Specialist focuses on evaluating and improving quality processes and product standards. Both roles are essential in regulated industries but differ in scope and responsibilities.

Is document control a stressful job?

A QA Document Control Associate's role involves managing and maintaining quality documentation, which can be detail-oriented and deadline-driven. While it may involve some pressure to ensure compliance and accuracy, the job typically offers a structured environment with clear procedures, making it less stressful than roles with high ambiguity or rapid changes.

What is a QA Document Control Associate?

QA Document Control Associates are professionals responsible for managing, organizing, and maintaining documentation related to quality assurance (QA) processes within an organization. Their duties often include ensuring that all documents comply with regulatory standards, are properly stored, and are easily accessible for audits or inspections. They play a crucial role in supporting quality systems by controlling document revisions, distribution, and archiving to maintain accuracy and compliance. This role is essential in industries like pharmaceuticals, biotechnology, and manufacturing where precise documentation is required by law or industry standards.

What are the key skills and qualifications needed to thrive as a QA Document Control Associate?

To thrive as a QA Document Control Associate, you need strong attention to detail, organizational skills, and a foundational understanding of quality assurance principles, often supported by a degree in a scientific or technical field. Familiarity with document management systems (DMS), regulatory compliance software, and standards such as ISO 9001 is typically required. Excellent communication, problem-solving abilities, and a proactive mindset are standout soft skills in this role. These competencies ensure accurate documentation, regulatory compliance, and efficient quality processes crucial to organizational success.

What are some common challenges faced by a QA Document Control Associate, and how can they be managed effectively?

QA Document Control Associates often encounter challenges such as managing large volumes of documents, ensuring version control, and meeting strict regulatory compliance deadlines. Staying organized through robust document management systems and maintaining clear communication with cross-functional teams are key strategies for success. Regular training on industry regulations and utilizing checklists can also help prevent errors and maintain document integrity. Proactivity and attention to detail are especially important in this role, as even small oversights can have significant impacts on audits and quality assurance processes.

What cities near Raleigh, NC are hiring for Qa Document Control Associate jobs?

Cities near Raleigh, NC with the most Qa Document Control Associate job openings:

Qa Document Control Associate jobs near you

QC Associate II

Integrated Resources INC

Raleigh, NC

Contractor

Re-posted 16 days ago

Job description

Company Description

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Qualification & Job Responsibilities:

The Quality Control Raw Materials Associate II will possess technical knowledge regarding Quality Control Raw Material methodologies. The position requires but is not limited to the following: demonstrated technical and analytical abilities, solid oral and written communication skills; ability to communicate with management and peers effectively and in a timely manner, effective organizational skills, developing or demonstrated problem solving skills, developing or demonstrated instrument/method troubleshooting skills, general knowledge of USP/PhEur regulations and compliance. 

Responsibilities

The ideal candidate will perform qualification of Raw Materials, protocols and reports, perform testing such as compendial analysis on raw materials per the USP, PhEur, JP or ACS monographs and general chapters in support of manufacturing based on cGMP's and internal procedures. 

Qualifications 

The candidate must demonstrate knowledge and proficiency in analytical techniques. Compendial experience per USP/PhEur is a must. 

Additional techniques include titrimetry, pH, osmolalrity, Karl Fisher, polarimetry, spectroscopy, Total Organic Carbon and Conductivity. Additional experience in chromatography, including HPLC and GC, is a plus. 


Qualifications

Education

B.S. degree in the Sciences, preferably Chemistry, with 3-5 years' experience in a cGMP environment, preferably in the pharmaceutical or biotechnology industry. 

A.S. Degree in Chemistry with 6-9 years' experience in a cGMP environment, preferably in the pharmaceutical or biotechnology industry.


Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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