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Document Control Associate Jobs in East Providence, RI

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 ...

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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 ...

QMS Specialist

Middleborough, MA · On-site

$54K - $68K/yr

Coach employees on QMS procedures, document control, audit readiness, nonconforming product handling, and quality best practices. EDUCATION AND EXPERIENCE * Associate degree in quality, engineering ...

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 ...

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 ...

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 ...

Compile document packages to be uploaded to customer portals Document Control * Process document ... Associate's degree is preferred * SAP experience is a plus * Administrative or quality-related ...

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 ...

Maintain complete, accurate, and inspection-ready documentation. What we expect of you We are all ... Associate's degree and 8 years of directly related experience OR * Bachelor's degree and 4 years of ...

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Document Control Associate information

See East Providence, RI salary details

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How much do document control associate jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for document control associate in East Providence, RI is $26.69, according to ZipRecruiter salary data. Most workers in this role earn between $18.65 and $33.89 per hour, depending on experience, location, and employer.

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 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.

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 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.

What are the most commonly searched types of Document Control jobs in East Providence, RI?

The most popular types of Document Control jobs in East Providence, RI are:

What cities near East Providence, RI are hiring for Document Control Associate jobs?

Cities near East Providence, RI with the most Document Control Associate job openings:

Infographic showing various Document Control Associate job openings in East Providence, RI as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 21% Part Time, and 4% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $55,508 per year, or $26.7 per hour.

Quality Control Associate

Amgen

West Greenwich, RI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted yesterday

New


Job description

Career CategoryOperationsJob Description

Join Amgen's Mission of Serving Patients

At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Associate Quality Control

What you will do

Let's do this. Let's change the world. In this vital role you will be responsible for activities including microbiology & analytical testing, sample and data management and equipment and instrumentation operation and maintenance in a highly dynamic, team environment.

This role is expected to work a 10-hour shift Saturday - Tuesday, from 6:45AM-5:15PM.

Responsibilities include:

  • Responsible for one or more of the following activities in Quality Control including analytical testing, characterization, sample and data management

  • Perform sample collection and sample handling to support GMP operations

  • Perform testing and possible data review for compendia, non-compendia methods, and routine laboratory procedures

  • Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks

  • Operate and maintain specialized laboratory equipment and instrumentation

  • Participate in laboratory investigations and audits as necessary

  • Perform general laboratory housekeeping activities

  • Maintain training compliance and proficiency

  • At all times, comply with safety guidelines, cGMPs and other applicable regulatory requirements

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a good teammate with these qualifications.

Basic Qualifications:

  • High school/GED + 2 years [Job Code's Discipline and/or Sub-Discipline] work experience OR

  • Associate's + 6 months [Job Code's Discipline and/or Sub-Discipline] work experience OR

  • Bachelor's

Preferred Qualifications:

  • Experience in a regulated biotechnology/pharmaceutical lab environment

  • Professional work experience in a fast-paced, flexible GxP Microbiology Laboratory

  • Experience executing microbiological test methods (ie. Endotoxin, PCR, Growth Promotion Testing)

  • Experience supporting Environmental and Clean Utility monitoring programs

  • Demonstrated written and oral communication skills with ability to write effective science-based quality and compliance documents

  • Demonstrated ability to be flexible and adaptable to support business needs

  • Experience executing endotoxin, media qualification and sterility testing

  • Demonstrated proficiency with electronic systems (LIMS, LMES, Trackwise, etc.)

  • Exposure to Operational Excellence initiatives including Lean Manufacturing and 5S

  • Demonstrated project management and presentation skills, and proven ability to manage priorities effectively

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts

  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan

  • Stock-based long-term incentives

  • Award-winning time-off plans

  • Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

Apply now and make a lasting impact with the Amgen team.

careers.amgen.com

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Application deadline

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

Sponsorship

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

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Salary Range

62,571.90USD -84,656.10USD