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Quality Associate Jobs in Washington (NOW HIRING)

Mpr Associates, Inc.

Quality Engineer

Alexandria, VA

$77K - $99K/yr

As the Quality Engineer at MPR, you play a key role in ensuring the MPR quality assurance program ... About MPR Founded in 1964, MPR Associates provides independent engineering and consulting services ...

Mpr Associates, Inc.

Quality Engineer

Alexandria, VA · On-site

$77K - $99K/yr

About MPR Founded in 1964, MPR Associates provides independent engineering and consulting services ... Support quality assurance processes across projects in diverse regulated industries including ...

Mpr Associates, Inc.

Quality Engineer

Alexandria, VA · On-site

$77K - $99K/yr

About MPR Founded in 1964, MPR Associates provides independent engineering and consulting services ... Support quality assurance processes across projects in diverse regulated industries including ...

Elite Technical

Quality Inspector

Manassas, VA · On-site

Quality InspectorIntroduction: Our client, a leading federal defense contractor, is seeking a ... Associates degree in Electronics, Computer Science, or Mechanical Engineering plus 4 years of ...

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All JobsQuality Associate JobsQuality Associate Jobs in Washington

Quality Associate information

See Washington salary details

$12

$30

$57

How much do quality associate jobs pay per hour?

As of Jul 19, 2026, the average hourly pay for quality associate in Washington is $30.50, according to ZipRecruiter salary data. Most workers in this role earn between $20.67 and $35.67 per hour, depending on experience, location, and employer.

What are Quality Associates?

Quality Associates are professionals responsible for ensuring that products or services meet established quality standards before reaching customers. They assist in monitoring production processes, performing inspections, and documenting quality issues or defects. Quality Associates also help implement quality control procedures and work closely with other departments to resolve any quality-related problems. Their role is essential in maintaining compliance with regulatory requirements and ensuring customer satisfaction.

What is the difference between Quality Associate vs Quality Technician?

AspectQuality AssociateQuality Technician
Required CredentialsHigh school diploma or equivalent; some roles may prefer certifications like ASQ CQPAHigh school diploma; certifications like CQTA are common but not always required
Work EnvironmentOffice settings, manufacturing floors, labsManufacturing plants, labs, production lines
Employer & Industry UsageManufacturing, healthcare, aerospace, automotiveManufacturing, electronics, pharmaceuticals
Common Search & ComparisonOften compared for entry-level quality rolesSimilar roles but more technical focus

While both roles focus on quality assurance, a Quality Associate typically handles documentation, audits, and process improvements, often in office or administrative settings. A Quality Technician usually performs hands-on inspections, testing, and data collection directly on the production floor. Both roles are essential in maintaining product quality but differ in their daily tasks and work environments.

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

To thrive as a Quality Associate, you need attention to detail, knowledge of quality control principles, and often a degree in science, engineering, or a related field. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and documentation software is typically required. Strong analytical thinking, communication skills, and problem-solving abilities help you collaborate across teams and address process issues effectively. These skills and qualities ensure that products and processes consistently meet standards, minimizing errors and maintaining compliance.

What are some common challenges Quality Associates face when working on cross-functional teams?

Quality Associates often collaborate with departments like manufacturing, engineering, and regulatory affairs to ensure product quality standards are met. One common challenge is balancing differing priorities—while production teams may be focused on output and speed, Quality Associates must prioritize compliance and thorough documentation. Navigating these competing interests requires strong communication skills and a proactive approach to problem-solving. Building positive relationships across teams and fostering a culture of quality can help overcome these challenges and ensure successful outcomes.

What Does a Quality Associate Do?

A quality associate works as part of a team, typically in the manufacturing industry, to inspect and audit a factory to ensure that production follows the necessary protocols and delivers the expected results. In this role, your responsibilities involve all aspects of quality control. You test procedures and make adjustments as required to meet goals and deadlines. As part of your duties, you log your findings and implement a plan for the smooth operation of the line for the long-term. Some people in this career specialize in a particular facet of the manufacturing process.

More about Quality Associate jobs
What are the most commonly searched types of Quality jobs in Washington? The most popular types of Quality jobs in Washington are:
What are popular job titles related to Quality Associate jobs in Washington? For Quality Associate jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Quality Associate jobs in Washington look for? The top searched job categories for Quality Associate jobs in Washington are:
What cities in Washington are hiring for Quality Associate jobs? Cities in Washington with the most Quality Associate job openings:
Quality Associate jobs near you

QA Associate - Pharmaceutical Manufacturing

Granules

Manassas, VA • On-site

$55K - $65K/yr

Full-time

Posted 2 days ago

Job description

Description:

Granules Consumer Health, LLC is located in Manassas, Virginia. We have over 106 employees and annual revenue of $76.64 million. We serve as Granules’ packaging facility and front-end division for private label over the counter (OTC) products in the US. We offer OTC generics that meet the highest level of quality at an affordable cost. As such, we are well-established on bulk supply through efficiencies garnered through manufacturing, integration and a high level of regulatory compliance. We are dedicated to excellence in manufacturing, quality, and customer service.


The QA associate for documentation ensures compliance with cGMP and internal policies, procedures, and specifications. This position is responsible for performing inspections, batch record review, and quality system functions in accordance with cGMP and related company SOP’s, state, federal and local laws as applicable. This person should be knowledgeable of cGMP requirements, FDA regulations and ICH guidelines.


Job Duties & Responsibilities


  • Manage and maintain company document control and archival systems (hardcopy and electronic) in compliance with internal procedures and policies as well as regulatory requirements.
  • Manage the routing, review, approval, distribution and archival of new and revised controlled documents.
  • Track controlled documents through the issuance of Document Control numbers, logbooks, change requests, and document status reports.
  • Archive and maintain hardcopy and electronic copies of batch records files, audit files, vendor files, product, label files and change history files.
  • Control and issuance of labeling components.
  • Manage all document control logbooks and spreadsheets.
  • Perform the release of finished product batches packaged.
  • Provide new hire training on GMP’s, Safety, and Pharmacovigilance and maintain the training program documentation.
  • Ensure standard operating procedures are periodically reviewed for relevance and accuracy in compliance with company policies and procedures.
  • Collaborate with team members to ensure timely deliverables for documentation.
  • Ensuring all documents are up to date with respect to version control and issuance
  • Perform and support maintenance and closure activities of documents such as reports, protocols exceptions/deviations, CAPAs, change controls and complaints.
  • cGMP Compliance in Document Control.
  • Any other activity as assigned by the Supervisor


Requirements:


Knowledge & Skills


  • cGMP compliance within the pharmaceutical manufacturing industry.
  • Writing and maintaining cGMP documentation.
  • Analyze data/information and resolve complex issues.
  • Verbal and written communication skills.
  • Work and communicate with cross-functional teams.
  • Multiple priorities and re-prioritize tasks.


Experience & Education


  • At least two (2) years’ experience in a quality assurance role in a cGMP-regulated environment.
  • A college Degree preferably in Sciences (i.e. Pharmacy, Biology, Chemistry etc.)


Physical Requirements/Working Environment


  • While performing the duties of this job, the employee is regularly required to, stand, sit, talk, hear, and use hands and fingers to operate a computer and telephone keyboard.
  • Specific vision abilities required by this job include close vision requirements due to computer work.
  • Ability to sit at a computer terminal for an extended period of time.
  • Light to moderate lifting up to 10-15 lbs. is required.
  • Ability to work in a confined area.


We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.