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Quality Associate Jobs in Monroe, WA (NOW HIRING)

Quality Associate II Shift Schedule is 2100-0730, Wednesday-Saturday The Quality Associate II position plays a key role in supporting the cGMP quality operations for the Bothell Manufacturing Plant ...

Associate Quality Production Specialist Company: The Boeing Company Boeing Defense, Space & Security (BDS) has an exciting opportunity for an Associate Quality Production Specialist to join the Site ...

Associate Quality Production Specialist Company: The Boeing Company Boeing Defense, Space & Security (BDS) has an exciting opportunity for an Associate Quality Production Specialist to join the Site ...

Associate Quality Production Specialist Company: The Boeing Company Boeing Defense, Space & Security (BDS) has an exciting opportunity for an Associate Quality Production Specialist to join the Site ...

Job Title: QA Associate Location: Bothell, WA*100% onsite Work Schedule: Sunday-Wednesday, 9PM - 7:30AM PST* Top Skills - - Documentation Review experience - Scientific Degree - Experience working in ...

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Quality Associate information

See Monroe, WA salary details

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How much do quality associate jobs pay per hour?

As of May 28, 2026, the average hourly pay for quality associate in Monroe, WA is $28.45, according to ZipRecruiter salary data. Most workers in this role earn between $19.28 and $33.27 per hour, depending on experience, location, and employer.

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.

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 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 does a QA associate do?

A QA associate is responsible for inspecting and testing products or processes to ensure they meet quality standards and specifications. They document issues, collaborate with production teams, and may use tools like checklists or testing software to identify defects and improve quality. Attention to detail and knowledge of quality procedures are essential for this role.

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 most commonly searched types of Quality jobs in Monroe, WA? The most popular types of Quality jobs in Monroe, WA are:
What cities near Monroe, WA are hiring for Quality Associate jobs? Cities near Monroe, WA with the most Quality Associate job openings:

Quality - QA Associate

Omni Inclusive

Bothell, WA • On-site

Other

This job post has expired today. Applications are no longer accepted.


Job description

Quality Associate II

Shift Schedule is 2100-0730, Wednesday-Saturday

The Quality Associate II position plays a key role in supporting the cGMP quality operations for the Bothell Manufacturing Plant (Jump). Primary responsibilities include the review of cGMP controlled documents such as SOPs, forms, completed batch records, and conducts walkthroughs of on the floor activities to ensure product and processes meet cGMP and internal standards. This role directly supports Jump's release for infusion (RFI) timeline from the date of manufacture and will support all activities for routine clinical and commercial product release at Jump with an emphasis on supporting Manufacturing with a Quality perspective within a regulated cGMP environment. The primary focus of the QA Associate role will be to support routine clinical and commercial production to ensure consistent compliance with regulatory and industry expectations. Assist the QA department in maintaining the quality focused culture at Jump by ensuring documentation is complete, accurate and that batch records are executed in accordance with approved and effective standard operating procedures and specifications.

Qualification Requirements (Knowledge, Skills and Abilities): Education Bachelor's degree in relevant science or engineering discipline is preferred. Minimum of Associates degree and/or equivalent combination of education and experience is required. Experience • 2-3 years of relevant cGMP experience. Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing are preferred. • Hands-on experience with batch record review and product disposition is preferred. • Strong computer skills with Word and Excel and other electronic manufacturing systems. • Detail oriented team player with effective planning, organization, time management and execution skills. • Proven experience working on teams where combined contribution, collaboration, and results were expected. • Must exercise accurate judgment and be able to evaluate information critically and decide upon appropriate course of action. • Ability to work in a high paced team environment. • Strong written and verbal skills.

Roles and Responsibilities • Review executed batch records to ensure compliance with approved procedures and communicate and resolve discrepancies with manufacturing operators or supervisors. • Conduct Quality on the Floor activities including quality walk-throughs of the production, testing and warehouse locations. • Execute Quality operations in support of Manufacturing and logistics • Provide Quality support to Manufacturing personnel on the floor; provide guidance during GMP events and initiation of deviation investigations. • Support the batch disposition process by ensuring that all required documents are accurately and properly completed, including all batch related deviations. • Oversee manufacturing operations during patient material receipt and drug product pack out. • May participate in revisions of Standard operating Procedures as needed.

Working Conditions • While performing the duties of this job, the employee is frequently required to stand; walk; sit; bend; stretch; use hands and fingers, with various manipulations; reach with hands and arms; and effectively communicate with others in the workplace, including the ability to make and promptly respond to audible cues and warnings. • May work in areas that may have strong magnets. • May work in areas with exposure to vapor phase liquid nitrogen and other chemicals. • Must be able to gown per requirements to enter manufacturing space. • Will be required to wear personal protective equipment (PPE) and other clean room garments daily. This may include, but not limited to safety shoes, safety glasses, aprons, face shields, lab coats, full body gowns, hairnets, gloves, and hearing protection.