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Quality Assurance Document Control Associate Jobs in Chepachet, RI

CEDENT

Quality Assurance Associate I

Cumberland, RI · On-site

The QA Associate II/III independently conducts quality assurance audits of production records ... SOPs, technical reports, validation documents, QA assessment, APRs, audit documents, change control ...

Amgen

Quality Control Associate

West Greenwich, RI · On-site

Associate Quality Control What you will do Let's do this. Let's change the world. In this vital ... Generate complete, accurate, and concise laboratory documentation using electronic systems and ...

Aerotek

Quality Assurance Associate

Southbridge, MA

$22.25 - $26.19/hr

Quality Assurance Associate The Quality Assurance Associate will be responsible for performing in ... This role requires the identification and verification of current documents, drawings, and ...

Aerotek

Quality Assurance Associate

Southbridge, MA · On-site

$22.25 - $26.19/hr

Quality Assurance Associate The Quality Assurance Associate will be responsible for performing in ... This role requires the identification and verification of current documents, drawings, and ...

Amgen

Sr Associate QA - Nights

West Greenwich, RI · On-site

... Control, and Facilities/Engineering staff regarding compliance and quality systems ... Author, review, and approve quality documents such as risk assessments, training materials ...

Emerson

Quality Assurance Specialist

Mansfield, MA

$60K - $68K/yr

... quality control assurance requirements * Review and approve special process documentation by ... Associate degree * Prior work experience within a quality assurance program/department

Emerson

Quality Assurance Specialist

Mansfield, MA

$60K - $68K/yr

... quality control assurance requirements * Review and approve special process documentation by ... Associate degree * Prior work experience within a quality assurance program/department

Emerson

Quality Assurance Specialist

Mansfield, MA

$60K - $68K/yr

... quality control assurance requirements * Review and approve special process documentation by ... Associate degree * Prior work experience within a quality assurance program/department

Emerson

Quality Assurance Specialist

Mansfield, MA

$60K - $68K/yr

... quality control assurance requirements * Review and approve special process documentation by ... Associate degree * Prior work experience within a quality assurance program/department

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Quality Assurance Document Control Associate information

See Chepachet, RI salary details

$12

$29

$52

How much do quality assurance document control associate jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for quality assurance document control associate in Chepachet, RI is $29.96, according to ZipRecruiter salary data. Most workers in this role earn between $20.91 and $38.08 per hour, depending on experience, location, and employer.

What is a quality assurance document control associate?

A Quality Assurance Document Control Associate is responsible for managing, organizing, and maintaining documentation related to quality assurance processes within an organization. They ensure that all quality documents, such as standard operating procedures (SOPs), work instructions, and records, are accurate, up-to-date, and comply with regulatory requirements. Their role often involves reviewing, issuing, archiving, and tracking documents, as well as supporting audits and ensuring that employees use the correct versions of documents. This position is critical in industries like pharmaceuticals, biotechnology, and manufacturing, where document control is vital for regulatory compliance and quality management.

What are the key skills and qualifications needed to thrive as a quality assurance document control associate?

To thrive as a Quality Assurance Document Control Associate, you need strong organizational skills, attention to detail, and familiarity with regulatory requirements, often supported by a degree in life sciences or a related field. Proficiency with document management systems (DMS), electronic quality management systems (eQMS), and standards such as ISO or FDA regulations is crucial. Effective communication, time management, and the ability to work meticulously under deadlines are valuable soft skills for this role. These competencies ensure the accuracy, compliance, and efficient handling of critical documentation, which is essential for maintaining quality standards in regulated industries.

What are the main challenges quality assurance document control associates face when managing document version control in regulated industries?

Quality Assurance Document Control Associates often encounter challenges ensuring all documents are current, accurate, and accessible to authorized personnel, especially in highly regulated industries like pharmaceuticals or medical devices. Managing version control requires meticulous attention to detail to prevent outdated documents from being used in production or audits. Additionally, coordinating timely reviews and approvals from multiple stakeholders can be complex, making strong organizational and communication skills essential for success in this role.

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

AspectQuality Assurance Document Control AssociateQuality Assurance Specialist
Primary RoleManage and maintain quality documentation, ensure document accuracy, control revisionsDevelop, implement, and monitor quality assurance processes and procedures
Required CredentialsTypically a high school diploma or associate degree; familiarity with document management systemsBachelor's degree in quality, engineering, or related field; certifications like CQE often preferred
Work EnvironmentOffice setting, regulated industries like pharmaceuticals, manufacturingLaboratory, manufacturing, or quality assurance departments in similar industries
Key FocusDocument control, compliance, record keepingProcess improvement, quality audits, compliance management

While both roles support quality assurance, the Document Control Associate primarily handles documentation and record management, whereas the Quality Assurance Specialist focuses on developing and overseeing quality processes. The Associate role is more administrative, while the Specialist role involves active process improvement and compliance oversight.

Quality Assurance Document Control Associate jobs near you

Document Control Associate (25598)

NEOTech

Westborough, MA • On-site

$25 - $28/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 9 days ago

Job description

Summary:
Creation and maintenance of assembly and customer documentation within the facility, in addition to coordinating ERP updates, as required.
Essential Duties and Responsibilities:
  • Upload, verify, edit and release bills of material into the ERP through new product introduction process.
  • Perform ERP updates as required to ensure that standard costs, lead-times, operation numbers, AVL, planner numbers, lot control switches, and all other relevant ERP data are current.
  • Assign ECO numbers and implement ECO changes in ERP.
  • Maintenance of ECO process and attach completed ECOs to the ERP system.
  • Update and link electronic documentation, as required.
  • Execute line-for-line reviews of documentation to identify bill of material changes between the ERP and the customer-provided documentation.
  • Create, maintain and distribute product folders, as required.
  • Support and follow all ISO standards related to the Company's various Quality Management Systems. These systems may include, but are not limited to, quality, the environment, health, safety and security.
  • Support all corporate and site 6S objectives.
  • Perform all other duties, as assigned.

Job Knowledge, Skills & Abilities:
  • Good technical/verbal communication.
  • Extremely high level of attention to detail.
  • Proficiency at operating photocopying and scanning equipment.
  • Ability to interpret basic customer specifications.
  • Proficient in MS Office Suite and electronic file management.
  • Working knowledge of ESD awareness and ISO.

Experience/Education:
  • High School Diploma or GED.
  • 1 year in a manufacturing environment preferred.

Benefits Offered: Comprehensive benefit package including medical, dental and vision coverage; company-paid basic life/AD&D insurance, short-term and long-term disability insurance; voluntary supplemental insurances, flexible spending accounts and employee assistance program (EAP). Sick Leave, Vacation Time, and company-paid Holidays are also provided as paid time off. NEOTech also provides a 401(k) Retirement Savings Plan option with a company match.
NEOTech is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran status, or any other characteristic protected by applicable federal, state, or local law.
NEOTech has a long-standing commitment to maintaining a safe, quality-oriented and productive work environment. We also want all employees to perform their duties safely and efficiently, in a manner that protects their interests and those of their co-workers. We recognize that alcohol and drug abuse pose a threat to the health and safety of NEOTech employees and to the security of the Company's equipment and facilities. For these reasons, NEOTech is committed to the elimination of drug and alcohol use and abuse in the workplace. Candidates being considered for hire must pass a pre-employment background check and drug test which include screening for illegal drugs and marijuana

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