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Document Control Associate Jobs in Fall River, MA

Emerson Group

Engineering Associate

Mansfield, MA · On-site

$70K - $85K/yr

Direct experience with product data management (PDM) and document control * Working knowledge of Solidworks, Windchill, Oracle, or similar software and ERP systems * Possess a mechanical aptitude in ...

Emerson

Engineering Associate

Mansfield, MA

$70K - $85K/yr

Direct experience with product data management (PDM) and document control * Working knowledge of Solidworks, Windchill, Oracle, or similar software and ERP systems * Possess a mechanical aptitude in ...

TERRACON

Project Assistant

Providence, RI · 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 ...

TERRACON

Project Assistant

Providence, RI · On-site

$24.48 - $34.38/hr

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

Aerotek

Material Handler

Warwick, RI · On-site

$16.25 - $19.75/hr

Apply strong attention to detail and perform quality checks related to materials and documentation ... Experience as a Material Handler, Warehouse Associate, Inventory Control Associate, Forklift ...

New

GDIT

Activity Security Representative (ASR) III

Taunton, MA

$17.50 - $20.50/hr

... document control. * Assist in the processing of inbound data and outbound data transfer files ... Bachelor's degree (Desired) Bachelor's degree counts as four years of experience, Associate ...

Leidos

Senior Configuration Analyst

Newport, RI · On-site

$59K - $106K/yr

Bachelor's degree or Associates degree and 4 years of configuration management experience to ... Prior experience using/supporting CMPro Document Control Software. * Hold an active US DoD security ...

Leidos

Senior Configuration Analyst

Newport, RI · On-site

$59K - $106K/yr

... document PEO SUB PMS4011/4013 Configuration Control Manual (CCM) of 16 January 2008. The candidate ... Bachelor's degree or Associates degree and 4 years of configuration management experience to ...

Leidos

Senior Configuration Analyst

Newport, RI · On-site

$59K - $106K/yr

... document PEO SUB PMS4011/4013 Configuration Control Manual (CCM) of 16 January 2008. The candidate ... Bachelor's degree or Associates degree and 4 years of configuration management experience to ...

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All JobsDocument Control Associate JobsDocument Control Associate Jobs in Fall River, MA

Document Control Associate information

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$26

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How much do document control associate jobs pay per hour?

As of Jul 23, 2026, the average hourly pay for document control associate in Fall River, MA is $26.59, according to ZipRecruiter salary data. Most workers in this role earn between $18.56 and $33.80 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Document Control Associate, and why are they important?

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.

Is document control a good career?

A career as a Document Control Associate involves managing and organizing company documents, ensuring accuracy and compliance with industry standards. It requires attention to detail, familiarity with document management systems, and often benefits from certifications like ISO or ISO-related training. The role offers stability and opportunities for advancement in industries such as manufacturing, construction, and pharmaceuticals.

What are Document Control Associates?

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.

Is a document controller an entry level job?

A document control associate is often considered an entry-level position, suitable for individuals with basic organizational skills and attention to detail. Some roles may require familiarity with document management software or industry-specific standards, but many employers provide on-the-job training for new hires.

What is a document control associate?

A document control associate is responsible for managing and maintaining company documents, ensuring they are accurate, organized, and accessible. They often use document management systems and follow established procedures to support quality assurance and regulatory compliance in various industries.

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.

How much is the salary of a document controller?

The salary of a document control associate typically ranges from $40,000 to $65,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced professionals with certifications can earn higher salaries, especially in industries like construction or engineering that require strong organizational skills and familiarity with document management software.
What are the most commonly searched types of Document Control jobs in Fall River, MA? The most popular types of Document Control jobs in Fall River, MA are:
What cities near Fall River, MA are hiring for Document Control Associate jobs? Cities near Fall River, MA with the most Document Control Associate job openings:
Document Control Associate jobs near you
Infographic showing various Document Control Associate job openings in Fall River, MA as of June 2026, with employment types broken down into 2% As Needed, 81% Full Time, 9% Part Time, 2% Temporary, 4% Contract, and 2% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $55,302 per year, or $26.6 per hour.
Senior Quality Systems Analyst

Senior Quality Systems Analyst

Johnson and Johnson

Raynham, MA • On-site, Remote

Full-time

Retirement, PTO

Posted 8 days ago

Job description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Quality
Job Sub Function:
Quality Systems
Job Category:
Professional
All Job Posting Locations:
Raynham, Massachusetts, United States of America, Remote (US)
Job Description:
Johnson & Johnson is currently recruiting for Senior Quality Systems Analyst-US Last Mile! This position can be performed remotely within United States. Remote work may be considered on a case-by-case basis and if approved by the business.
Position Summary:
The Sr Quality Systems Analyst executes quality system activities supporting US DePuy Synthes Commercial Quality (CQ), distribution sites, regional functions, and Last Mile field inventory managers. The role is responsible for supporting quality system data review, metrics reporting, document management, training process execution, and compliance activities that help maintain an effective Quality Management System for commercial activities in the US
Key responsibilities:
  • Support CQ and business partners on quality systems and compliance activities.
  • Compile and summarize quality data for reporting, Data Review Board, and Management Review.
  • Coordinate document control and training activities, including routing, release, assignments, completion monitoring, and records review.
  • Maintain quality records, including gap assessments, risk assessments, inspection tools, and related documentation.
  • Support nonconformance/CAPA, quality planning, change management, and effectiveness monitoring activities.
  • Communicate procedure changes, training requirements, quality expectations, and document updates to cross-functional partners.
  • undefined

Execute and support systems/processes in the following areas:
  • Quality metrics and governance reviews
  • Training and document control processes
  • Audit/inspection readiness and response
  • Quality planning, change management, and risk-based assessments
  • Quality issue and effectiveness monitoring
  • Quality system applications, including DMS, LMS, QEM, ETQ, Windchill, Summit, Compliance Wire, ERP, and warehouse management systems
  • GxP coaching and guidance for business partners

External and internal interactions:
  • DePuy Synthes Quality & Regulatory Compliance
  • DePuy Synthes Commercial/Sales Operations and Supply Chain partners
  • DePuy Synthes external Sales Agents
  • Notified bodies, health authorities, and state regulatory agencies as applicable
  • Other internal or external partners supporting compliant commercial distribution and field inventory operations. (i.e. Marketing)

Required Qualification and Core Competencies for the role:
  • Minimum bachelor's degree required. Preferred degree areas include Engineering, Science, Business, Quality, Regulatory Compliance, or related fields. Associate degree with relevant regulated industry experience may be considered.

Experience:
  • 7 years of relevant work experience in a regulated healthcare, medical device, pharmaceutical, consumer products, distribution, commercial quality, or quality systems environment.
  • Working knowledge of applicable FDA regulations, ISO 13485, ISO 9001, and quality system requirements relevant to commercial distribution and field inventory environments.
  • Experience supporting quality systems, document control, training compliance, quality metrics, audits, nonconformance management, corrective action processes, or related compliance activities.
  • Experience using quality system IT platforms such as Windchill, ETQ, DMS, LMS, QEM, Summit, change control systems, ERP systems, warehouse management systems, or related tools preferred.

Required skills and certifications:
  • Communicate and collaborate effectively with cross-functional partners.
  • Follow established procedures, complete assigned work accurately and on time, maintain organized records, and escalate issues when needed.
  • Apply critical thinking, problem-solving, and root cause analysis to support issue resolution.
  • Demonstrate working knowledge of standard quality system requirements and documentation practices.
  • Use Microsoft Office, data analysis and quality system applications
  • Preferred experience with Windchill, ETQ, Summit, ERP or warehouse management systems.
  • Preferred data analysis experience includes pivot tables, lookups, Power BI, Tableau, or related visualization tools.
  • Preferred experience includes audit preparation, inspection readiness, regulatory responses, or health authority interactions.
  • Preferred certifications or training include Lean, Six Sigma, 5S, ASQ, ISO-13485, Good Distribution Practices, supplier quality, or other quality improvement methods.

Job location: United States: Domestic travel up to 25% may be required based on business needs.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers . internal employees contact AskGS to be directed to your accommodation resource.
Required Skills:
Preferred Skills:
The anticipated base pay range for this position is :
$94,000.00 - $151,800.00
Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation -120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year
Holiday pay, including Floating Holidays -13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave - 80 hours in a 52-week rolling period10 days
Volunteer Leave - 32 hours per calendar year
Military Spouse Time-Off - 80 hours per calendar year
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

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