This role offers an exciting opportunity to lead a high-performing Quality Assurance team in a regulated pharmaceutical environment. You will play a critical role in ensuring compliance ...
This role offers an exciting opportunity to lead a high-performing Quality Assurance team in a regulated pharmaceutical environment. You will play a critical role in ensuring compliance ...
Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of ...
Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of ...
Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of ...
Quick apply
Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of ...
Seran BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of ...
Seran BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of ...
Associate Quality Engineer - Redmond, OR
$67K - $101K/yr
Job Summary Responsible for providing basic quality support to the Division including complaint investigation, resolution, and reporting. Assist with routine product evaluations, set basic quality ...
Associate Quality Engineer - Redmond, OR
$67K - $101K/yr
Job Summary Responsible for providing basic quality support to the Division including complaint investigation, resolution, and reporting. Assist with routine product evaluations, set basic quality ...
Associate Quality Engineer - Redmond, OR
Redmond, OR · On-site
$67K - $101K/yr
Job Summary Responsible for providing basic quality support to the Division including complaint investigation, resolution, and reporting. Assist with routine product evaluations, set basic quality ...
Associate Quality Engineer - Redmond, OR
Redmond, OR · On-site
$67K - $101K/yr
Job Summary Responsible for providing basic quality support to the Division including complaint investigation, resolution, and reporting. Assist with routine product evaluations, set basic quality ...
Director of Quality
Portland, OR · On-site
$160K - $190K/yr
Nagle and Associates has been retained by Kanto Corporation to execute the Director of Quality, executive search. A Leadership Opportunity to Build and Lead Enterprise Quality Our firm is partnering ...
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Director of Quality
Portland, OR · On-site
$160K - $190K/yr
Nagle and Associates has been retained by Kanto Corporation to execute the Director of Quality, executive search. A Leadership Opportunity to Build and Lead Enterprise Quality Our firm is partnering ...
Plant Manager
$118K - $139K/yr
Minimum 5 years of overall manufacturing experience in a leadership role, including responsibility for P&L, safety, quality, associate development, production, and financial and inventory management
New
Plant Manager
$118K - $139K/yr
Minimum 5 years of overall manufacturing experience in a leadership role, including responsibility for P&L, safety, quality, associate development, production, and financial and inventory management
New
Quality Inspector
Clackamas, OR · On-site
Pay Rate Low: 20 | Pay Rate High: 22 Quality Inspector Location: Fully Onsite - Clackamas, OR ... Associate's degree in related field + 4 years of relevant experience INDBH #LI-DNI
Quality Inspector
Clackamas, OR · On-site
Pay Rate Low: 20 | Pay Rate High: 22 Quality Inspector Location: Fully Onsite - Clackamas, OR ... Associate's degree in related field + 4 years of relevant experience INDBH #LI-DNI
Associate Procurement Quality Manager Does the thought of joining one of the fastest-growing, privately held data center companies sound exciting to you? Do you enjoy collaborating with team members ...
Associate Procurement Quality Manager Does the thought of joining one of the fastest-growing, privately held data center companies sound exciting to you? Do you enjoy collaborating with team members ...
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 ...
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 ...
Seran 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 ...
Seran 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 ...
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 ...
New
Quick apply
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 ...
New
Company Description We're Nagarro. We are a digital product engineering company that is scaling in a big way! We build products, services, and experiences that inspire, excite, and delight. We work ...
Company Description We're Nagarro. We are a digital product engineering company that is scaling in a big way! We build products, services, and experiences that inspire, excite, and delight. We work ...
Quality Technician
Mcminnville, OR · On-site
$18.25 - $24.75/hr
... Associate's or Bachelor's degree in a related field is desired * A combination of relevant ... Prior experience in quality assurance or control is preferred * Computer proficiency, including ...
Quality Technician
Mcminnville, OR · On-site
$18.25 - $24.75/hr
... Associate's or Bachelor's degree in a related field is desired * A combination of relevant ... Prior experience in quality assurance or control is preferred * Computer proficiency, including ...
Quality Technician
Mcminnville, OR · On-site
$18.25 - $24.75/hr
... Associate's or Bachelor's degree in a related field is desired * A combination of relevant ... Prior experience in quality assurance or control is preferred * Computer proficiency, including ...
Quality Technician
Mcminnville, OR · On-site
$18.25 - $24.75/hr
... Associate's or Bachelor's degree in a related field is desired * A combination of relevant ... Prior experience in quality assurance or control is preferred * Computer proficiency, including ...
Quality Technician
$18.25 - $24.75/hr
... Associate's or Bachelor's degree in a related field is desired * A combination of relevant ... Prior experience in quality assurance or control is preferred * Computer proficiency, including ...
Quality Technician
$18.25 - $24.75/hr
... Associate's or Bachelor's degree in a related field is desired * A combination of relevant ... Prior experience in quality assurance or control is preferred * Computer proficiency, including ...
Quality Technician
$18.25 - $24.75/hr
... Associate's or Bachelor's degree in a related field is desired * A combination of relevant ... Prior experience in quality assurance or control is preferred * Computer proficiency, including ...
Quality Technician
$18.25 - $24.75/hr
... Associate's or Bachelor's degree in a related field is desired * A combination of relevant ... Prior experience in quality assurance or control is preferred * Computer proficiency, including ...
Quality Manager
Boring, OR · On-site
$130/hr
Quality Manager Kelly ® Science & Clinical is seeking a Quality Manager for a direct-hire position ... Effectively lead, manage, develop, coach, and evaluate team members and associates at various ...
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Quality Manager
Boring, OR · On-site
$130/hr
Quality Manager Kelly ® Science & Clinical is seeking a Quality Manager for a direct-hire position ... Effectively lead, manage, develop, coach, and evaluate team members and associates at various ...
Quality Engineer
Tualatin, OR · On-site
$80K - $100K/yr
ASQ CQE (Certified Quality Engineer) and / or CQIA (Certified Quality Improvement Associate) desired * 3+ years of relevant Manufacturing experience in the Aerospace and/or Semiconductor industry ...
Quality Engineer
Tualatin, OR · On-site
$80K - $100K/yr
ASQ CQE (Certified Quality Engineer) and / or CQIA (Certified Quality Improvement Associate) desired * 3+ years of relevant Manufacturing experience in the Aerospace and/or Semiconductor industry ...
Quality Associate information
See Oregon salary details
$11.69 - $15.50
8% of jobs
$15.50 - $19.32
16% of jobs
$19.44 is the 25th percentile. Wages below this are outliers.
$19.32 - $23.13
24% of jobs
The median wage is $23.54 / hr.
$23.13 - $26.94
15% of jobs
$30.51 is the 75th percentile. Wages above this are outliers.
$26.94 - $30.75
13% of jobs
$30.75 - $34.57
6% of jobs
$34.57 - $38.38
9% of jobs
$38.38 - $42.19
6% of jobs
$42.19 - $46
1% of jobs
$46 - $49.81
1% of jobs
$49.81 - $53.63
0% of jobs
$11
$28
$53
How much do quality associate jobs pay per hour?
As of Jul 13, 2026, the average hourly pay for quality associate in Oregon is $28.47, according to ZipRecruiter salary data. Most workers in this role earn between $19.33 and $33.32 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?
| Aspect | Quality Associate | Quality Technician |
|---|---|---|
| Required Credentials | High school diploma or equivalent; some roles may prefer certifications like ASQ CQPA | High school diploma; certifications like CQTA are common but not always required |
| Work Environment | Office settings, manufacturing floors, labs | Manufacturing plants, labs, production lines |
| Employer & Industry Usage | Manufacturing, healthcare, aerospace, automotive | Manufacturing, electronics, pharmaceuticals |
| Common Search & Comparison | Often compared for entry-level quality roles | Similar 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 Oregon? The most popular types of Quality jobs in Oregon are:
What are popular job titles related to Quality Associate jobs in Oregon? For Quality Associate jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Quality Associate jobs in Oregon look for? The top searched job categories for Quality Associate jobs in Oregon are:
What cities in Oregon are hiring for Quality Associate jobs? Cities in Oregon with the most Quality Associate job openings:
Full-time
Medical, Dental, Vision
Re-posted 27 days ago
Lonza rating
8.3
Based on 42 frontline employees who took The Breakroom Quiz
23rd of 74 rated pharmaceutical
Job description
The actual location of this job is in Bend, Oregon (USA). Relocation assistance is available for eligible candidates and their families, if needed.
This role offers an exciting opportunity to lead a high-performing Quality Assurance team in a regulated pharmaceutical environment. You will play a critical role in ensuring compliance, strengthening quality systems, and supporting the delivery of life-changing therapies.
This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.
What you will get
The full list of our global benefits can also be found at: https://www.lonza.com/careers/benefits
What you will do
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together.
Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.Ready to shape the future of life sciences? Apply now.
This role offers an exciting opportunity to lead a high-performing Quality Assurance team in a regulated pharmaceutical environment. You will play a critical role in ensuring compliance, strengthening quality systems, and supporting the delivery of life-changing therapies.
This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.
What you will get
- An agile career and dynamic working culture
- An inclusive and ethical workplace
- Compensation programs that recognize high performance
- Medical, dental, and vision insurance
- Opportunities for leadership development and career growth
- Access to Lonza's global benefits
The full list of our global benefits can also be found at: https://www.lonza.com/careers/benefits
What you will do
- Lead Quality Assurance functions, including training, quality systems, and audit readiness
- Manage and develop QA teams supporting GMP production and documentation processes
- Ensure quality systems remain compliant, effective, and aligned with business needs
- Support manufacturing and development teams to meet regulatory and internal standards
- Review and approve quality documents, procedures, and specifications
- Oversee deviation management, CAPA processes, and stakeholder communication
- Support internal audits, client audits, and regulatory inspections
- Bachelor's degree or equivalent experience in a relevant field
- Extensive experience in the pharmaceutical industry, including work in CDMO environments
- Proven leadership experience managing teams in regulated quality environments
- Experience supporting or leading regulatory inspections and audits
- Strong knowledge of GMP and quality systems
- Excellent communication skills with the ability to engage diverse stakeholders
- Ability to manage multiple priorities and drive results in a fast-paced environment
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together.
Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.Ready to shape the future of life sciences? Apply now.
About Lonza
Sourced by ZipRecruiter