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Quality Management Assistant Jobs in Oregon (NOW HIRING)

Coordinate, implement, and maintain the laboratory's Quality Management System in collaboration ... Supervise QA Associate and/or Assistant positions, including interviewing, making hiring ...

Coordinate, implement, and maintain the laboratory's Quality Management System in collaboration ... Supervise QA Associate and/or Assistant positions, including interviewing, making hiring ...

Coordinate, implement, and maintain the laboratory's Quality Management System in collaboration ... Supervise QA Associate and/or Assistant positions, including interviewing, making hiring ...

Quality Engineer

Gresham, OR · On-site

$76K - $98K/yr

Monitor construction quality and support project staff in the performance of day-to-day activities applicable to the Quality Management System. * Assist multiple project teams with the development of ...

Quality Engineer

Gresham, OR

$76K - $98K/yr

Monitor construction quality and support project staff in the performance of day-to-day activities applicable to the Quality Management System. * Assist multiple project teams with the development of ...

... the Quality Management System. • Participate in internal audits and support corrective action activities resulting from audit findings. • Assist manufacturing and support functions in ...

New

Quality Technician

Wilsonville, OR · On-site

$47K - $69K/yr

... the Quality Management System. • Participate in internal audits and support corrective action activities resulting from audit findings. • Assist manufacturing and support functions in ...

... * Assist with customer audits, technical presentations, qualification reviews, and proposal ... Proficiency with Microsoft Office Suite, Adobe Acrobat, and quality management systems.

... * Assist with customer audits, technical presentations, qualification reviews, and proposal ... Proficiency with Microsoft Office Suite, Adobe Acrobat, and quality management systems.

... the Quality Management System. • Participate in internal audits and support corrective action activities resulting from audit findings. • Assist manufacturing and support functions in ...

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Showing results 1-20

Quality Management Assistant information

See Oregon salary details

$53.9K

$79.8K

$108.4K

How much do quality management assistant jobs pay per year?

As of Jul 25, 2026, the average yearly pay for quality management assistant in Oregon is $79,825.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,100.00 and $89,900.00 per year, depending on experience, location, and employer.

What are some common challenges Quality Management Assistants face when supporting compliance initiatives?

Quality Management Assistants often encounter challenges such as staying current with evolving regulatory standards and ensuring consistent documentation practices across departments. They may also need to coordinate with various teams to gather accurate data for audits and quality reports, which can be time-sensitive and require attention to detail. Proactive communication and a strong understanding of quality procedures help overcome these challenges, enabling smooth compliance processes and continuous improvement within the organization.

What is the highest paid assistant job?

Among assistant roles, executive assistants and administrative assistants with specialized skills or experience in industries like finance or law tend to have the highest salaries. Senior or executive-level assistants often earn higher wages, especially when supporting top executives or working in large organizations. Certifications and proficiency with tools like Microsoft Office or project management software can also influence pay levels.

What is the salary for a quality manager?

The salary for a quality manager typically ranges from $70,000 to $120,000 annually, depending on experience, industry, and location. They often hold certifications like Six Sigma or ISO auditor training and work in manufacturing, healthcare, or technology sectors.

What is the difference between Quality Management Assistant vs Quality Control Technician?

AspectQuality Management AssistantQuality Control Technician
CertificationsISO 9001, Six Sigma basicsISO 9001, Six Sigma, Quality Control certifications
Work EnvironmentOffice settings, administrative tasks, documentationManufacturing floors, product testing, inspection
Employer & IndustryManufacturing, healthcare, service sectorsManufacturing, production plants, food industry

While both roles support quality assurance, the Quality Management Assistant focuses on documentation, process support, and administrative tasks related to quality management systems. In contrast, the Quality Control Technician is more involved in hands-on product inspection, testing, and ensuring quality standards are met during production.

What are Quality Management Assistants?

Quality Management Assistants are professionals who support the quality assurance and quality control processes within an organization. They help implement and monitor quality management systems, assist with audits, maintain documentation, and ensure compliance with relevant standards and regulations. Their work helps organizations deliver products or services that consistently meet customer and regulatory requirements. Quality Management Assistants often collaborate with various departments to improve processes and resolve quality issues.

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

To thrive as a Quality Management Assistant, you need a solid understanding of quality assurance processes, attention to detail, and often a background in business, science, or related fields. Familiarity with ISO standards, quality management systems (QMS) like ISO 9001, and proficiency in data analysis tools or spreadsheets is typically required. Strong organizational skills, effective communication, and problem-solving abilities help you excel in supporting quality initiatives. These skills ensure accurate documentation, compliance with regulations, and continuous process improvement within the organization.

What is the role of a quality assistant?

A quality management assistant supports quality assurance processes by collecting data, maintaining documentation, and assisting with inspections and audits. They help ensure products or services meet company standards and may use tools like quality management software to track compliance and improvements.

What does a QA assistant do?

A QA (Quality Assurance) assistant supports the quality management process by inspecting products, documenting defects, and ensuring compliance with standards. They often use testing tools and follow established procedures to help maintain product quality and assist in continuous improvement efforts.
What are the most commonly searched types of Quality Management jobs in Oregon? The most popular types of Quality Management jobs in Oregon are:
What cities in Oregon are hiring for Quality Management Assistant jobs? Cities in Oregon with the most Quality Management Assistant job openings:
QA Manager

QA Manager

Actalent

Happy Valley, OR

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago


Job description

Job Title: Quality Assurance ManagerJob Description

The Quality Assurance Manager oversees the laboratory’s Quality Management System to ensure consistent quality, robust policies, and regulatory compliance. This role leads continuous improvement initiatives, verifies adherence to standards, and supports the laboratory in achieving its mission and objectives. The Quality Assurance Manager serves as a key liaison between laboratory operations, regulatory requirements, and clients, while managing QA staff and fostering a strong quality culture.

Responsibilities
  • Lead the laboratory’s quality function proactively and foster a culture of continual improvement in quality, processes, and procedures.
  • Coordinate, implement, and maintain the laboratory’s Quality Management System in collaboration with the Laboratory Director, Laboratory Manager, Group Leaders, and laboratory staff.
  • Oversee document control and quality records, ensuring that controlled documents and records are accurate, current, and compliant with applicable standards.
  • Manage training documentation to ensure personnel are properly trained, qualified, and documented for their assigned responsibilities.
  • Plan, coordinate, and support internal and external audits, including scheduling, execution, documentation, and follow-up on findings.
  • Administer corrective and preventive actions (CAPA) and continuous improvement activities, ensuring timely resolution and effective preventive measures.
  • Coordinate proficiency testing, including scheduling, reporting results, and following up on any issues or non-conformances identified.
  • Manage supplier qualification and traceability processes, ensuring that suppliers meet quality and regulatory expectations.
  • Serve as archivist for Good Laboratory Practice (GLP) study-specific records, ensuring proper storage, organization, and traceability of critical documentation.
  • Ensure internal audits of the Quality Management System are performed at least annually to maintain compliance with applicable standards and accreditation programs.
  • Identify areas of non-conformance and opportunities for improvement, and drive actions to address findings from audits and reviews.
  • Prepare special reports for regulatory agencies and clients, including summary reports of analytical results, external audit responses, FDA data packages, and ODA data packages.
  • Verify that new method validations and method improvements comply with internal policies and applicable regulatory requirements.
  • Write, review, and maintain Quality Management System standard operating procedures (SOPs) and related documentation in collaboration with the Quality Assurance Unit, Laboratory Manager, Laboratory Director, and other relevant departments.
  • Review controlled laboratory documentation for compliance, accuracy, and quality, ensuring alignment with SOPs, laboratory practices, and regulatory requirements.
  • Perform procedural audits of laboratory methods against applicable SOPs, laboratory procedures, and regulatory requirements to confirm accuracy and adherence.
  • Provide periodic reports to the Laboratory Manager and Laboratory Director on laboratory quality performance, audit observations, findings, non-compliances, and non-conformances.
  • Make recommendations for corrective actions and process improvements to enhance laboratory quality and compliance.
  • Coordinate Annual Quality Review Meetings with laboratory management and compile data and information throughout the year to prepare the annual Management Review of the Quality System report.
  • Coordinate and manage verification and maintenance of scheduled calibration for laboratory support equipment to ensure accurate and reliable operation.
  • Assist sales and marketing teams by responding to quality assurance-related inquiries from existing and potential clients.
  • Coordinate and conduct laboratory meetings to communicate updates on laboratory operations, regulatory changes, quality improvements, and quality issues.
  • Coordinate and deliver quality assurance training for laboratory personnel to maintain and enhance quality awareness and competence.
  • Supervise QA Associate and/or Assistant positions, including interviewing, making hiring recommendations, training new employees, planning and assigning work, directing daily activities, and appraising performance in accordance with organizational policies and applicable laws.
Essential Skills
  • Strong leadership skills with the ability to influence, guide, and develop teams in a laboratory environment.
  • Bachelor’s degree in Chemistry or a relevant scientific discipline.
  • Minimum 2 years (5–10 years ideal) of quality assurance experience in regulatory compliance, preferably at a corporate or national level.
  • Experience in a high-volume, wide-scope laboratory environment.
  • Experience with ISO or comparable quality management systems and standards.
  • Experience with GLP (Good Laboratory Practice) or equivalent regulatory frameworks.
  • Strong reading and writing skills, including the ability to draft and revise SOPs, reports, and manuals.
  • Strong presentation skills, with the ability to communicate technical and quality-related information clearly to diverse audiences.
  • Advanced math skills, including exponents, logarithms, statistics, and related quantitative concepts.
  • Demonstrated ability to perform QA/QC procedures and audits in a laboratory setting.
  • Proven problem-solving and analytical skills to identify root causes and implement effective corrective and preventive actions.
  • Experience collaborating across departments and leading cross-functional teams.
  • Experience managing change and driving continuous improvement within a quality or laboratory environment.
  • Previous laboratory experience, preferably in an analytical laboratory setting.
Additional Skills & Qualifications
  • Experience with ISO, NELAP, GLP, or equivalent accreditation or regulatory programs at a corporate or national level.
  • Experience preparing and responding to external audits and regulatory inspections.
  • Experience preparing regulatory and client-facing reports such as analytical summaries, audit responses, and data packages.
  • Experience managing document control systems and quality records in a regulated environment.
  • Experience coordinating proficiency testing and supplier qualification programs.
  • Comfort working with complex quality documentation and multiple concurrent projects.
  • Strong interpersonal and communication skills to effectively interact with laboratory staff, management, clients, and external stakeholders.
Work Environment

This role operates in a fast-paced analytical laboratory environment with a team of approximately six chemists, reporting into laboratory leadership. The typical schedule runs from 9:00 a.m. to 5:30 p.m. The position involves regular use of analytical laboratory equipment and instruments, with possible exposure to hazardous chemicals and solvents. Work requires frequent repetitive hand and wrist movements and the ability to hear and understand verbal instructions clearly. Reasonable accommodations are available for qualified individuals with disabilities. The workplace offers designated free parking in a downtown location and a collaborative, quality-focused culture. The organization provides a comprehensive benefits package that includes medical and vision insurance with a high level of employer premium coverage, dental insurance, health savings account options with employer contributions, flexible spending accounts, supplemental insurance options, legal and identity protection services, a 401(k) plan, paid time off, and 13 paid holidays. Employees also have access to partnerships with well-known retail brands’ employee stores. The company regularly hosts monthly food events such as dinners, happy hours, and catered meals, along with a summer barbecue and family-friendly events like a "Kids to Work" day. A bonus program has historically provided an annual bonus approximately equivalent to one month’s salary, subject to business performance and prorated for employees who join partway through the year.

Job Type & Location

This is a Permanent position based out of Portland, OR.

Pay and Benefits

The pay range for this position is $72000.00 - $72000.00/yr.

Benefits: Medical/vision insurance (company covers 100% of EE premium and 90% of dependent and HSA- company covers 100% of premium and contributes to HSA every month), dental insurance, LTD, FSA, supplemental insurance, LegalShield/IDShield, 401(k), PTO, 13 paid holidays, and partnership with Adidas and Columbia employee store.

Workplace Type

This is a fully onsite position in Portland,OR.

Application Deadline

This position is anticipated to close on Aug 3, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

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