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Quality Control Manager Jobs in Ridgefield, WA (NOW HIRING)

Genentech

QC Specialist, Master Data

Hillsboro, OR

The HTO Quality Control (QC) Team is looking for an individual interested in managing simple to moderately complex sets of Master Data that support QC operations. This role will collaborate with ...

Jireh Semiconductor

Yield (QC) Technician

Hillsboro, OR · On-site

$20 - $28/hr

Jireh Semiconductor is seeking a Yield Technician to join their Quality Control team. This position ... performance power management solutions. AOS's portfolio of products targets high-volume ...

MSR-FSR

QA/QC Cleanroom Technician

Hillsboro, OR · On-site

$20.50 - $26.25/hr

Operations Manager SUMMARY: Operations QAQC Cleanroom Technicians are responsible for performing ... Keeps emotions under control; Remains open to others' ideas and tries new things. • Motivation ...

MSR-FSR

QA/QC Cleanroom Technician

Hillsboro, OR

$20.50 - $26.25/hr

Operations Manager SUMMARY: Operations QAQC Cleanroom Technicians are responsible for performing ... Keeps emotions under control; Remains open to others' ideas and tries new things. Motivation - Sets ...

MSR-FSR

QA/QC Cleanroom Technician

Hillsboro, OR · On-site

$20.50 - $26.25/hr

Operations Manager SUMMARY: Operations QAQC Cleanroom Technicians are responsible for performing ... Keeps emotions under control; Remains open to others' ideas and tries new things. · Motivation ...

Southland Industries

QA/QC Professional

Vancouver, WA · On-site

$71K - $100K/yr

Inform management of potential problems. * Reviews project requirements for Quality Assurance/Quality Control and help project teams identify roles, responsibilities and expectations before the ...

CRH

QC Technician/Safety Coordinator

Portland, OR · On-site

$25 - $32/hr

QC Technician/Safety Coordinator Architectural Products Group Portland, Oregon, United States Job ... Work alongside managers/employees on EHS issues * Recognize safety hazards or unsafe work practices ...

Alpha Iron, LLC

Be Seen First

QC Inspector - Level II (UT/MT)

Ridgefield, WA · On-site

$30 - $40/hr

Alpha Iron is seeking a Certified Welding Inspector who will work closely with the Quality Manager to control the quality of our manufacturing process. Perform quality control tasks that include but ...

CRH

QC Technician/Safety Coordinator

Portland, OR

$25 - $32/hr

Support manufacturing team in producing the highest quality products * Test all products and raw ... Work alongside managers/employees on EHS issues * Recognize safety hazards or unsafe work practices ...

HTG, Inc.

IT Equipment Cleaning/Quality Control

Ridgefield, WA · On-site

$20 - $25.50/hr

Salary: 19/hour Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * Enter product details and specifications into ...

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Quality Control Manager information

See Ridgefield, WA salary details

$32.4K

$86.3K

$137.4K

How much do quality control manager jobs pay per year?

As of Jun 12, 2026, the average yearly pay for quality control manager in Ridgefield, WA is $86,292.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,200.00 and $106,100.00 per year, depending on experience, location, and employer.

What does a Quality Control Manager do?

A Quality Control Manager is responsible for overseeing and ensuring the quality of products or services within an organization. They develop and implement quality control procedures, inspect products, and monitor operations to ensure compliance with industry standards and regulations. Additionally, they analyze quality data, identify areas for improvement, and work closely with other departments to resolve quality issues. Their goal is to maintain high standards and minimize defects or errors in the final output.

What is the difference between Quality Control Manager vs Quality Assurance Supervisor?

AspectQuality Control ManagerQuality Assurance Supervisor
Primary FocusInspecting products and processes to identify defectsDeveloping and implementing quality systems and procedures
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentManufacturing, production lines, labsQuality departments, process improvement teams
Employer UsageManufacturers, factories, production facilitiesCompanies with formal quality management systems

Both roles focus on quality but differ in scope. The Quality Control Manager primarily inspects products to catch defects, while the Quality Assurance Supervisor develops systems to prevent defects. Understanding these differences helps in choosing the right career path or hiring focus.

What are the biggest challenges a Quality Control Manager typically faces when implementing new quality standards?

One of the main challenges Quality Control Managers encounter is ensuring that all team members understand and consistently adhere to newly implemented quality standards. This often involves extensive training, clear documentation, and continuous monitoring to address resistance to change or misunderstandings. Additionally, balancing the need for thorough quality checks with production deadlines can be demanding, requiring strong communication and problem-solving skills to align quality goals with operational efficiency. Collaborative efforts with production, engineering, and compliance teams are essential to successfully integrate new standards while maintaining workflow.

What Does a Quality Control Manager Do?

As a quality control manager, your responsibilities are to ensure that your company’s products are up to industry standards by inspecting items and overseeing the efficiency of production and manufacturing processes. Your job duties as a quality control manager include coordinating between company management and production departments, implementing strategies to maximize employee efforts, and evaluating processes on manufacturing and production lines. Your focus is on quality assurance of both processes and output to minimize the number of problems that inspectors might identify when visiting the company.

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

To thrive as a Quality Control Manager, you need expertise in quality assurance processes, analytical skills, and a background in science or engineering, often supported by a relevant degree. Familiarity with quality management systems (such as ISO 9001), statistical analysis software, and internal auditing tools is typically required. Strong leadership, problem-solving abilities, and excellent communication help drive team performance and foster a culture of continuous improvement. These skills ensure that products meet strict standards, reduce defects, and maintain customer satisfaction in a competitive market.
More about Quality Control Manager jobs
What cities near Ridgefield, WA are hiring for Quality Control Manager jobs? Cities near Ridgefield, WA with the most Quality Control Manager job openings:
Quality Control Manager jobs near you
QC Specialist, Master Data

QC Specialist, Master Data

Genentech, Inc.

Hillsboro, OR • On-site

Full-time

Posted 27 days ago

Genentech rating

9.0

Company rating: 9.0 out of 10

Based on 21 frontline employees who took The Breakroom Quiz

7th of 71 rated pharmaceutical

Job description

Hillsboro Technical Operations (HTO) is a drug product & finished goods manufacturing organization responsible for the reliable delivery of Roche's commercial portfolio & pipeline products. The Operations organization at HTO is divided into three value streams, which combine to produce millions of units of life-saving medicine every year to patients around the world.
The Opportunity:
Do you have a passion for consistent data and understand how this can be achieved through clear and consistent Master Data? Are you a problem solver that believes most or all issues can be linked to a process flaw? Then you may be the person we are looking for. The HTO Quality Control (QC) Team is looking for an individual interested in managing simple to moderately complex sets of Master Data that support QC operations. This role will collaborate with internal and external departments (e.g. QC Operations, Database System Developers, Business Analysts, Manufacturing, Packaging, External Quality, Control System Scientists, Product Technical Leads etc.) to maintain and improve contemporary relevance of QC Master Data. This role will gain a deeper understanding of how the master data is utilized and how it can be improved as they own/perform activities that support/improve lab operations using Good Manufacturing/Laboratory Practices. These activities will include conducting minor deviation investigations, owning Corrective and Preventive Actions (CAPAs), owning Change Request Actions, performing periodic reporting, data review and generation of certificates of test/analysis, direct material release, and analytical equipment administration.
  • You will create, update, test various sets of Master Data and end-user defined system settings that enables consistent execution, collection, transaction, storage, analysis, and reporting of analytical/microbiological tests and activities performed by Quality Control Operations. Supported Software Systems include: Labware LIMS, Biovia, Molecular Devices SoftMax Pro, SAP, Mettler Toledo LabX, Waters Empower Chromatography Data System, Veeva, and ValGenesis.
  • You will be the site representative on System Enhancement Teams and User Communities of Practice Teams, communicate system changes and best practices to local system users and coordinate initial and maintain continuous end user training materials/content for supported systems.
  • You will perform Direct Material Release and review / generate Drug Product Certificates of Analysis, as needed.
  • You will lead or participate in minor Quality Control Investigations (e.g.: Out of Specifications, Out of Expectations, Over Action Limits, local and global process deviations) using established Root Cause Analysis tools and generating data-based impact assessments within established timelines.
  • You will collaborate with key stakeholders to identify and execute Corrective and Preventive Action Plans, completing assigned actions through self or others with tact and effective communication skills.
  • You will author, review, and/or approve various business process & compliance related documents such as, standard operating procedures, work instructions, monitoring protocols, monitoring reports, gap assessments, and risk assessments.
  • You will participate in cross functional teams that ensure safety, quality, delivery, engagement and cost objectives are sustained / exceeded. You will own, delegate and/or drive actions that result from these teams.

Who You Are
  • You hold a Bachelor's of Science degree with 4-7 years of experience in the pharmaceutical industry, quality control and/or database management or 8+ years of experience with an Associates/Vocational Degree. 3 years of experience working in a cGMP or similarly regulated environment is required.
  • You possess a working understanding of database management/relational tables, Operational Excellence tools, cGMP regulations and industry guidelines related to biological processing. You consistently apply this understanding when executing your tasks. We would be even more delighted, if you have experience building reporting tools such as tableau dashboards.
  • You work independently within standard operating procedures, guidelines, and policies to execute role based accountabilities and have the judgment / discretion to escalate matters of significance in a timely manner, ensuring efficient operations and regulatory compliance.
  • You are able to assess various changes/issues related to quality control or database management to define/determine next actions required to bring about a desired outcome or mitigate risks associated with these changes/issues to the QC organization.
  • You have strong verbal and written communication skills with ability to summarize minor to moderate problems that drive timely informed decisions and completion of simple to moderate actions.
  • You have a curious open mindset and continuously share information with others as a means to foster effective cross functional teams

Work Environment/Physical Demands/Safety Considerations
  • You will be working on site in a flexible open space work environment with random visits to a QC laboratory environment that requires laboratory gowning (lab coat, goggles, gloves)
  • You will work on/interact with computerized systems/screens for long periods of time (6-8 hours)
  • You may be required to lift up to 25lbs
  • You may have to work with hazardous materials and chemicals

Relocation benefits are available for this position.
The expected salary range for this position based on the primary location of Oregon is $77,770 to $144,430. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Benefits
Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

What Genentech employees say

Pay

Benefits

Hours and flexibility

Workplace

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About Genentech

Sourced by ZipRecruiter

A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

South San Francisco, CA, US

Year founded

1976

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