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Document Control Associate Jobs in Fall River, MA

Cipla

QC Sampling Associate

Fall River, MA · On-site

$25 - $29/hr

Job Title: QC Sampling Associate FLSA Classification : Full-Time, Non-Exempt/Hourly Professional ... Document sampling activities in logbooks, sampling records, and electronic systems (SAP/ILMS) in a ...

Cipla

QC Sampling Associate

Fall River, MA

$25 - $29/hr

Job Title: QC Sampling Associate FLSA Classification : Full-Time, Non-Exempt/Hourly Professional ... Document sampling activities in logbooks, sampling records, and electronic systems (SAP/ILMS) in a ...

flowcontrol

Inventory Control Specialist

Lincoln, RI · On-site

$16.75 - $21.75/hr

Position Summary The Inventory Control Associate is responsible for maintaining accurate inventory ... documentation of cycle count activities. • Support Lean, 5S, and continuous improvement ...

flowcontrol

Inventory Control Specialist

Lincoln, RI · On-site

$16.75 - $21.75/hr

Position Summary The Inventory Control Associate is responsible for maintaining accurate inventory ... documentation of cycle count activities. • Support Lean, 5S, and continuous improvement ...

flowcontrol

Inventory Control Specialist

Lincoln, RI · On-site

$16.75 - $21.75/hr

Position Summary The Inventory Control Associate is responsible for maintaining accurate inventory ... documentation of cycle count activities. • Support Lean, 5S, and continuous improvement ...

Adecco

Quality Engineering Technician

East Providence, RI · On-site

$28 - $35/hr

Associate degree, technical training, or quality related coursework in a related field preferred. * Experience in quality, manufacturing, engineering, inspection, or document control role required.

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 ...

Emerson

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 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 ...

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 ...

L3HHCM20

Experienced, Cyber Intelligence

Fall River, MA

$92K - $171K/yr

Fall River, MA Job Schedule: 9/80 L3Harris is seeking a Senior Associate, Cyber Intelligence ... Manage classified document and media control, ensuring proper accountability, storage, inventory ...

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Document Control Associate information

See Fall River, MA salary details

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How much do document control associate jobs pay per hour?

As of Aug 12, 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 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 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.

QC Sampling Associate

Cipla

Fall River, MA • On-site

$25 - $29/hr

Full-time, Other

Posted 24 days ago

Job description

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates.
Job Title: QC Sampling Associate
FLSA Classification: Full-Time, Non-Exempt/Hourly Professional
Work Location: Fall River, MA
Work Hours: General Shift: 8:300 AM - 5:00 PM (may vary based on business needs)
Reports To: Quality Control Manager
Hourly Rate: $25 - $29
Duties and Responsibilities:
The general duties and responsibilities of the Quality Control Lab Technician include but are not limited to the following:
  • Perform sample withdrawal for all incoming raw materials, packing materials, water including but not limited to receipt, logging distribution and destruction.
  • Update all sample information in SAP as per company procedures.
  • Complete data entry as required.
  • Oversee temperature and humidity monitoring for retention and sample storage rooms.
  • Conduct sample loading in stability chambers and submitting stability samples as per schedule.
  • Provide general housekeeping in the QC lab and any other functional activity as assigned by management.
  • Maintaining and updating the retention rooms of raw materials as required.
  • Cleaning of sampling area and sampling accessories as per approved SOPs.
  • Ensure all sampling activities comply with cGMP, data integrity, and safety requirements.
  • Follow contamination-control practices during sampling, including gowning and cleanroom behavior when applicable.
  • Accurately label, log, and submit samples to the QC laboratory with complete documentation.
  • Maintain and verify cleanliness and readiness of sampling tools and equipment.
  • Support material status control by ensuring sampled materials are properly segregated and labeled.
  • Document sampling activities in logbooks, sampling records, and electronic systems (SAP/ILMS) in a timely and accurate manner.
  • Assist in investigations related to deviations, out-of-specification (OOS) results, or sampling errors, as required.
  • To participate in GDP, cGMP, and safety training programs.
  • Maintain compliance with site safety policies and participate in EHS initiatives.
  • Support audit and inspection readiness by ensuring sampling documentation is complete and inspection-ready at all times.
  • Coordinate and dispatch samples to contract testing laboratories (CTLs) or other InvaGen/Cipla laboratories as per approved procedures and testing requirements.
  • Maintain stock of sampling equipment and consumables.
  • Other duties as assigned.

Education and Experience:
  • Minimum of High School Diploma or equivalent education credential (ex. GED) required.
  • Proficient user of Microsoft Office Programs to include Word, Excel, Outlook, PowerPoint, and other lab-related systems.
  • 2 years' work experience in a pharmaceutical, raw materials sampling activity.
  • Associates degree or higher in Chemistry, Laboratory Science, or related fields of study from an accredited institution. (Preferred)
  • Proficiently speak English as a first or second language
  • Have excellent organization, learning and teaching skills required to work in teams
  • Ability to understand and analyze complex data.
  • Working knowledge of Microsoft Office programs and other scientific based software.
  • Experience in pharmaceuticals is a plus.

Professional and Behavioral Competencies
  • Hourly position.
  • Full time
  • Must be willing to work in a pharmaceutical packaging setting.
  • Must be willing and able to work any assigned shift ranging from first or second shift.
  • Work schedule may be Monday to Friday.
  • Must be willing to work some weekends based on business needs as required by management.
  • Must possess a positive, professional attitude toward work and willingness to cooperate with co-workers and supervisors.
  • No remote work available
  • No employment sponsorship or work visas.

Working conditions
This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. The role may be assigned on a work-shift basis, where required (Day, Evening, Night). Weekend or Holiday work may be requested or required. Long periods of standing up/walking during working hours; ability to ascent/decent ladders; and able to lift to 35 pounds.
GLOBAL COMPANY
Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.
Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.
CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.)
About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited.
EEO Statement
Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

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