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Quality Associate Jobs in Bend, OR (NOW HIRING)

Jeld-Wen, Inc.

Quality Specialist

Bend, OR · On-site

JELD-WEN is currently seeking a Quality Specialist to join our growing team. External Summary ... Our associates are dedicated to bringing beauty and security to the spaces that touch our lives ...

Jeld-Wen Inc.

Quality Specialist

Bend, OR · On-site

JELD-WEN is currently seeking a Quality Specialist to join our growing team. External Summary ... Our associates are dedicated to bringing beauty and security to the spaces that touch our lives ...

Ryan Companies

Quality Field Engineer

Bend, OR

$76K - $98K/yr

The Quality Engineer ensures that all phases of all mission-critical projects performed by the company or its subcontractors are carried out with the desired level of quality from inception through ...

Protouch Staffing

Associate Chiropractor

Bend, OR

$80K - $130K/yr

We are seeking a motivated Associate Chiropractor to join a growing practice and provide high-quality chiropractic care to patients. This role offers the opportunity to work in a collaborative ...

Title Nine Sports Inc

SALES ASSOCIATE

Bend, OR · On-site

If you're looking for a fun environment and love quality women's workout wear, then Title Nine is the place for you! Sales Associate: * Work with customers to ensure proper fit and style; recommend ...

Sunriver Brewing Company

Warehouse Associate

Sunriver, OR · On-site

$17.50 - $21/hr

Warehouse Associate Hours: Full Time (38 hours/week) Sunriver Brewing Company is seeking a detail-oriented warehouse associate with a passion for helping produce the highest quality craft beer. We ...

Sunriver Brewing Company

Warehouse Associate

Sunriver, OR · On-site

$17 - $22/hr

Warehouse Associate Hours: Full Time (38 hours/week) Sunriver Brewing Company is seeking a detail-oriented warehouse associate with a passion for helping produce the highest quality craft beer. We ...

Ross Stores

Retail Associate

Redmond, OR · On-site

$16.25 - $18.50/hr

Our focus has always been bringing our customers a constant stream of high-quality brands and on ... The Associate makes eye contact, smiles, and greets all Customers in a courteous and friendly ...

Ross Stores

Retail Associate

Redmond, OR · On-site

$16.25 - $18.50/hr

Our focus has always been bringing our customers a constant stream of high-quality brands and on ... The Associate makes eye contact, smiles, and greets all Customers in a courteous and friendly ...

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Showing results 21-40

All JobsQuality Associate JobsQuality Associate Jobs in Bend, OR

Quality Associate information

See Bend, OR salary details

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How much do quality associate jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for quality associate in Bend, OR is $28.41, according to ZipRecruiter salary data. Most workers in this role earn between $19.28 and $33.22 per hour, depending on experience, location, and employer.

What is a quality associate?

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 Bend, OR? The most popular types of Quality jobs in Bend, OR are:
What are popular job titles related to Quality Associate jobs in Bend, OR? For Quality Associate jobs in Bend, OR, the most frequently searched job titles are:
What job categories do people searching Quality Associate jobs in Bend, OR look for? The top searched job categories for Quality Associate jobs in Bend, OR are:
What cities near Bend, OR are hiring for Quality Associate jobs? Cities near Bend, OR with the most Quality Associate job openings:
Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Bend, OR as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 4% Contract, and 1% Nights. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $59,099 per year, or $28.4 per hour.

Associate Director of Quality Assurance, Operations

Serán BioScience

Bend, OR

Full-time

Posted 29 days ago

Job description

Serán is seeking a QA Associate Director,who oversees the day-to-day operations of the Quality Assurance department with oversite of clinical manufacturing and warehouse activities in addition to disposition of raw materials and drug products.  Required attributes include a results-driven and broad-minded quality assurance professional with extensive experience in compliance and regulations, quality systems management, investigations, training and mentoring, client relations, performance management, and change management.  Extensive experience with direct or quality oversite of manufacturing operations is required.

The successful candidate will have excellent problem-solving skills and will identify critical quality objectives, develop cross-functional, collaborative, and creative teams, and improve, adapt, and execute practical solutions in competitive and fast-paced environments.
Supervisory Responsibilities
  • Leads and mentors Quality Assurance personnel.
  • Recruits, interviews, hires and trains new staff. 
  • Oversees daily workflow of the department. 
Responsibilities
  • Leads and implements continuous improvement initiatives to reduce risk and improve efficiency for the company’s quality systems and department operations
  • Management and scheduling of department operations
  • Oversees and conducts review and approval of Investigations, CAPAs, Complaints, and Change Management
  • Review and approval of SOPs, batch records, raw material records, and certificates of conformance/compliance
  • Responsible for Quality oversight of activities involving raw material, drug product manufacturing, packaging, labeling, and warehouse activities
  • Assures cGMP compliance systems and processes are in place to support raw material and drug product review, release, storage, and shipping
  • Defines and maintains a strong people management, training, and engagement culture to ensure a high and constantly improving right first-time rate
  • Supports internal audits, client audits and regulatory inspections
Required Skills and Experience
  • Expert knowledge of GMP guidelines and Quality expectations for preclinical and clinical phase manufacturing operations
  • In-depth understanding and application of cGMP principles, concepts, practices, and standards 
  • Experience with regulatory inspections by the FDA and EU authorities 
  • Ability to influence diverse stakeholders and drive accountability and decision-making cross functionally 
  • Demonstrated ability to partner with other functional groups to achieve business objectives 
  • Experience organizing and managing group responsibilities while working independently with minimal oversight
  • Time and project management skills with the ability to multi-task and meet deadlines
  • Excellent verbal and written communication skills
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside of the company 
  • Excellent organizational skills and attention to detail
  • Strong analytical and problem-solving skills
  • Strong supervisory and leadership skills
Education and Experience
  • Minimum of a bachelor’s degree, preferably in a scientific discipline.  An advanced degree is preferred
  • 10+ years previous GMP and Quality experience in the Pharmaceutical industry with quality oversite of Oral Solid Dose manufacturing
  • Experience with regulatory inspections by the FDA and EU authorities

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.