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Quality Control Manager Jobs in Bend, OR (NOW HIRING)

Primary Duties The Quality Assurance Technician II is responsible for executing quality control ... Ensuring compliance with AAON's quality management system and applicable industry standards.

Primary Duties The Quality Assurance Technician II is responsible for executing quality control ... Ensuring compliance with AAON's quality management system and applicable industry standards.

Primary Duties The Quality Assurance Technician II is responsible for executing quality control ... Ensuring compliance with AAON's quality management system and applicable industry standards.

Primary Duties The Quality Assurance Technician II is responsible for executing quality control ... Ensuring compliance with AAON's quality management system and applicable industry standards.

Primary Duties The Quality Assurance Technician II is responsible for executing quality control ... Ensuring compliance with AAON's quality management system and applicable industry standards.

Primary Duties The Quality Assurance Technician II is responsible for executing quality control ... Ensuring compliance with AAON's quality management system and applicable industry standards.

Engineering Quality Lead

Redmond, OR · On-site

$76K - $98K/yr

Works with Quality Management to maintain the Quality Manual and participates in annual review and ... Develops quality control systems designed to ensure final products meet customer specifications and ...

Engineering Quality Lead

Redmond, OR · On-site

$76K - $98K/yr

Works with Quality Management to maintain the Quality Manual and participates in annual review and ... Develops quality control systems designed to ensure final products meet customer specifications and ...

Engineering Quality Lead

Redmond, OR · On-site

$76K - $98K/yr

Works with Quality Management to maintain the Quality Manual and participates in annual review and ... Develops quality control systems designed to ensure final products meet customer specifications and ...

Engineering Quality Lead

Redmond, OR · On-site

$76K - $98K/yr

Works with Quality Management to maintain the Quality Manual and participates in annual review and ... Develops quality control systems designed to ensure final products meet customer specifications and ...

Showing results 41-60

Quality Control Manager information

See Bend, OR salary details

$32.2K

$85.8K

$136.6K

How much do quality control manager jobs pay per year?

As of Sep 5, 2026, the average yearly pay for quality control manager in Bend, OR is $85,796.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,800.00 and $105,500.00 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 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 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 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.

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.

Is a Quality Control Manager a high paying job?

A Quality Control Manager typically earns a salary above the national average for managerial roles, with pay varying based on industry, experience, and location. They often require skills in inspection, testing, and quality assurance, and may hold certifications such as Six Sigma or ISO auditor training. Overall, it is considered a well-compensated position within manufacturing, production, and related sectors.

What is the work of a quality control manager?

A quality control manager oversees the inspection and testing of products or services to ensure they meet quality standards and specifications. They develop quality control procedures, analyze data, and coordinate with production teams to address issues, often using tools like inspection equipment and quality management systems. The role requires attention to detail, problem-solving skills, and knowledge of industry regulations.

What are the most commonly searched types of Quality Control jobs in Bend, OR?

The most popular types of Quality Control jobs in Bend, OR are:

What job categories do people searching Quality Control Manager jobs in Bend, OR look for?

The top searched job categories for Quality Control Manager jobs in Bend, OR are:

What cities near Bend, OR are hiring for Quality Control Manager jobs?

Cities near Bend, OR with the most Quality Control Manager job openings:

Infographic showing various Quality Control Manager 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 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $85,796 per year, or $41.2 per hour.

Quality Assurance Associate II/III (Swing Shift)

Serán BioScience

Bend, OR

Full-time

PTO

Re-posted 19 days ago


Key responsibilities

  • Review and approve production records, analytical data, and internal QA documentation.

  • Support investigations, manage CAPA processes, and participate in audits and inspections.

  • Document authorships, reviews, and approvals of SOPs, batch records, certificates of analysis, method validations, and equipment qualifications.


Job description

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 this role will be to support the daily activities of Serán’s Quality Assurance department by ensuring GMP regulations and internal SOPs are followed throughout the clinical manufacturing process. Essential task include reviewing and approving production records, analytical data, and internal QA documentation. Additional responsibilities include conducting risk analyses and investigations and participating in audits and inspections. Quality experience in a GMP Pharmaceutical Manufacturing setting is a requirement for this position with the ability for the title and compensation to commensurate with experience. 
 
This role will support the alternative manufacturing schedule from Monday - Thursday, beginning at 2:00 pm and ending at 1:00 am. Experience specific to Serán's manufacturing capabilities and confidence to make independent decisions in alignment with Company policies and risk mitigation philosophies will be critical to this role.  
 
 
Duties and Responsibilities
  • Documents authorships, reviews, and approves of SOPs, batch production and quality control (QC) records, certificates of analysis, method validations, and equipment qualifications
  • Applies working knowledge of best practices in GMP and understands how Quality integrates with other business areas
  • Initiates and oversees investigations
  • Manages corrective and preventive actions (CAPA)
  • Supports internal audits, client audits and regulatory inspections, with the potential to host 
  • Manages controlled document issuance and archival
  • Performs quality reviews with minimal oversight 
  • Communicates quality-related information to internal teams with minimal guidance
  • Responsibilities may increase in scope to align with company initiatives
  • Performs all other related duties as assigned
Required Skills and Abilities
  • Knowledge of GMP and FDA regulations for clinical trial materials; commercial knowledge is desirable but not required
  • Confident understanding of change control procedures, CAPA program, investigation and root cause analysis, and good documentation practices
  • Excellent organizational skills and attention to detail
  • Excellent time management skills with a proven ability to meet deadlines
  • Strong analytical and problem-solving skills
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the company
  • Demonstrates the ability to collaborate and work in cross-functional teams
  • Accepts feedback from a variety of sources and constructively manages conflict
  • Ability to prioritize tasks and to delegate them when appropriate
  • Excellent verbal and written communication skills
  • Ability to function well in a high-paced and at times stressful environment
  • Proficient with Microsoft Office Suite or related software
  • Ability to solve complex problems, take a new perspective on existing solutions, and exercise sound judgment based on the analysis of multiple sources of information to make independent decisions
Education and Experience
  • Bachelor’s degree, preferably in a scientific discipline
  • 3 years of GMP experience within a QC or QA role to meet the minimum qualifications for an Associate II
  • 6 years of GMP experience within a QC or QA role to meet the minimum qualifications for an Associate III
  • Pharmaceutical Manufacturing experience required, Oral Solid Dosage preferred
Physical Requirements
  • Prolonged periods of sitting or standing at a desk and working on a computer
  • Must be able to lift up to 15 pounds at times
  • Ability to wear required personal protective equipment (PPE), including safety glasses, hearing protection, hard hat, and safety shoes
  • Adheres to consistent and predictable in-person attendance
Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
 
Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
 
Benefits Summary:
Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
 
The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701

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.