ZipRecruiter

Log In

1

Utility Quality Control Jobs in Oregon (NOW HIRING)

City of Gresham, OR

Public Utility Worker 2

Gresham, OR · On-site

$28.60 - $36.49/hr

Control traffic for emergencies and daily tasks. Repair and maintain signs, markings and rights-of ... Qualities we are looking for: * An effective team player who values partnerships and forms ...

City of Gresham

Public Utility Worker 2

Gresham, OR · On-site

Control traffic for emergencies and daily tasks. Repair and maintain signs, markings and rights-of ... Qualities we are looking for: An effective team player who values partnerships and forms ...

WSP

Project Manager (Data Centers)

Portland, OR · On-site

$55 - $74.25/hr

Knowledge of QA/QC processes, risk management, and safety compliance in utility projects. Preferred Qualifications * Master's Degree in Engineering. • Professional Engineer (PE) license. • PMI ...

WSP

Project Manager (Data Centers)

Portland, OR · On-site +1

$55 - $74.25/hr

Knowledge of QA/QC processes, risk management, and safety compliance in utility projects. Preferred Qualifications * Master's Degree in Engineering. Professional Engineer (PE) license. PMI ...

IMEG

Senior Structural Engineer | Vancouver, WA

Portland, OR · On-site

$106K - $144K/yr

You will manage project scope, schedules, billings, quality control, and construction-phase ... Utility and power equipment qualification, especially transformers, reactors, and substations, plus ...

IMEG

Senior Structural Engineer | Vancouver, WA

Portland, OR · On-site

$106K - $144K/yr

You will manage project scope, schedules, billings, quality control, and construction-phase ... Utility and power equipment qualification, especially transformers, reactors, and substations, plus ...

SOLV Energy

Engineer 3

OR · On-site +1

The Engineer 3 will act as a technical Subject Matter Expert focused on value engineering, QA/QC, and independent technical judgment across utility-scale EPC projects. This role can be fully remote ...

previous page

Showing results 41-60

All JobsUtility Quality Control JobsUtility Quality Control Jobs in Oregon

Utility Quality Control information

What is utility quality control?

Utility Quality Control refers to the processes and procedures used to ensure that utility services—such as electricity, water, or gas—are delivered safely, reliably, and according to regulatory standards. Professionals in this field inspect and test systems and equipment, monitor compliance with safety and quality guidelines, and address any deficiencies. Their work helps maintain the integrity of utility infrastructure and ensures public safety. Utility Quality Control specialists often collaborate with engineers, field technicians, and regulatory agencies.

What are some common challenges faced by utility quality control professionals, and how can these be addressed on the job?

Utility Quality Control professionals often encounter challenges such as ensuring compliance with stringent regulatory standards, managing large volumes of inspection data, and coordinating with multiple departments to resolve quality issues. Staying up to date with evolving industry regulations and maintaining clear communication channels with field teams are essential strategies for overcoming these challenges. Proactive problem-solving and continuous training on new technologies and quality control methods can also help professionals navigate the demands of the role effectively.

What are the key skills and qualifications needed to thrive as a utility quality control professional, and why are they important?

To thrive as a Utility Quality Control professional, you need a strong background in quality assurance, inspection procedures, and utility regulations, often supported by relevant certifications or an engineering degree. Familiarity with industry standards, SCADA systems, and quality management software is typically required. Attention to detail, problem-solving abilities, and strong communication skills set top performers apart in this field. These skills ensure that utility services meet regulatory standards, maintain safety, and operate efficiently.

What is the difference between Utility Quality Control vs Utility Inspector?

AspectUtility Quality ControlUtility Inspector
Primary RoleEnsures quality standards in utility projects, overseeing compliance and testingInspects utility installations for safety, code adherence, and proper functioning
CertificationsQuality assurance certifications, technical trainingConstruction or safety inspection certifications
Work EnvironmentConstruction sites, testing labs, project officesConstruction sites, utility installation locations
Industry UsageUsed in utility construction, maintenance, and quality assuranceUsed in utility installation, safety inspections, and compliance checks

Utility Quality Control focuses on ensuring the overall quality and compliance of utility projects, often involving testing and quality assurance processes. Utility Inspectors primarily conduct on-site inspections to verify safety and adherence to codes during utility installations. While both roles work within the utility industry, Quality Control emphasizes quality standards, whereas Inspectors focus on safety and compliance.

What cities in Oregon are hiring for Utility Quality Control jobs?

Cities in Oregon with the most Utility Quality Control job openings:

Director, Quality Engineering & Computer System Assurance

Bend, OR

Seran BioScience
Manufacturing • 1 - 10 employees
Learn more about Seran BioScienceexternal

Full-time

PTO

Re-posted 29 days ago

Job description

Seran BioScience seeks a Director, Quality Engineering & Computer System Assurance (CSA) to oversee and provide strategic and operational leadership for the organization's validation, qualification, and computerized systems assurance programs.  This role will support GMP manufacturing, laboratory, and quality systems that stretch across clinical and commercial operations.
 
This position is responsible for establishing and maintaining a risk-based validation and CSA framework ensuring that facilities, utilities, equipment, analytical methods, processes, and computerized systems remain in a validated state throughout their lifecycle. The Director, Quality Engineering & CSA ensures all validation and data integrity activities comply with FDA, EU, and international regulatory requirements, including cGMP, GAMP guidance, and current regulatory expectations for data integrity.
 
The role partners with Engineering, Manufacturing, Quality Control, IT, Regulatory Affairs, and Technical Operations to ensure validated systems and processes enable safe, compliant, and reliable manufacturing of clinical and commercial products. The Director, Quality Engineering & CSA also serves as a key Quality leader during regulatory inspections, client audits, and internal quality reviews, and drives continuous improvement initiatives related to validation lifecycle management, computerized system assurance, and data governance.
Duties and Responsibilities
Strategic Leadership
  • Develops and implements the site strategy for Quality Engineering and Computer System Assurance(CSA) programs
  • Supports the establishment governance structures for risk-based validation lifecycle management including planning, execution, maintenance, and periodic review
  • Leads initiatives to modernize validation practices including CSA adoption, digital validation approaches, and automation lifecycle management
  • Defines key performance indicators (KPIs) and metrics to measure effectiveness of QualityEngineering and CSA programs
  • Provides leadership to cross-functional teams supporting validation, qualification, and system lifecycle activitie
Validation Lifecycle Oversight
  • Provides Quality leadership and oversight of validation programs including:
    • Facility, utility, and equipment qualification, Cleaning validation, Computerized systems validation / assurance, & Manufacturing automation systems
Key activities include:
  • Approval and oversight of validation lifecycle documentation including: 
    • Validation Master Plans (VMP), User Requirement Specifications (URS), Functional and Design Specifications, Risk assessments, IQ/OQ/PQ protocols and reports, & Validation summary reports
  • Ensures validation activities comply with internal procedures and regulatory requirements and remain aligned with the site Validation Master Plan
  • Provides quality oversight for commissioning, qualification, and validation activities in highly automated manufacturing environments
  • Ensures validated systems maintain a continuous state of control throughout their operational lifecycle
Computer System Assurance (CSA) & Data Integrity
  • Supports the design and implementation of the organization's Computer System Assurance (CSA) and Computerized System Validation (CSV) programs
  • Ensures computerized systems comply with data integrity principles (ALCOA++) and regulatory expectations
  • Oversees validation lifecycle management for computerized systems including:
    • Manufacturing Execution Systems (MES), Laboratory Information Management Systems (LIMS), Quality management systems, Electronic Batch Record Systems, & Enterprise resource planning systems
  • Implements risk-based testing approaches consistent with GAMP 5 and modern CSA methodologies
  • Leads initiatives to strengthen enterprise data integrity governance programs across manufacturing, laboratory, and quality systems
  • Supports system lifecycle activities including system upgrades, migrations, and decommissioning
Operational Quality Engineering Support
  • Provides QA oversight and approval for quality system elements impacting validated systems including:
    • Change control processes impacting validated systems and processes, Deviation and investigation management, Corrective and Preventive Actions (CAPA), Risk management and impact assessments, & Periodic reviews of validated systems
  • Ensures that validation and CSA programs remain aligned with corporate policies, regulatory guidance, and evolving industry standards
  • Provides QA support for technology transfer, new product introductions, and site capital projects
  • Serves as the Quality Engineering representative for site project teams implementing new equipment, systems, or manufacturing technologies
  • Supports troubleshooting of complex process or system issues impacting validated systems
  • Serve as subject matter expert for validation, computerized systems assurance, and data integrity during regulatory inspections and Client audits
  • Leads preparation and inspection readiness programs related to validation and data integrity
Leadership & People Management
  • Leads and develops a high-performing Quality Engineering and CSA organization
  • Provides mentoring, coaching, and professional development for technical staff
  • Establish clear departmental goals aligned with organizational quality and operational objectives
  • Conducts performance reviews and ensure staff maintain appropriate training and GMP qualifications
  • Fosters a culture of quality ownership, compliance, and continuous improvement
Required Knowledge and Skills
  • Broad knowledge of FDA and international regulations related to GMPs and Pharmaceuticals
  • Experience organizing and managing work responsibilities while working independently with minimal oversight
  • Deep expertise in Computer System Validation / Computer System Assurance
  • Validation lifecycle management, Data integrity regulations and industry guidance, Risk-based validation methodologies
  • Time and project management skills with the ability to multi-task and meet deadlines
  • Excellent verbal and written communication skills
  • Excellent interpersonal and customer service skills
  • Excellent organizational skills and attention to detail
  • Strong analytical and problem-solving skills
  • Strong supervisory and leadership skills
  • Ability to prioritize tasks and to delegate them when appropriate
  • Willingness to accept feedback from a variety of sources
  • Ability to constructively manage conflict
  • Ability to collaborate and work in cross-functional teams
  • Ability to function well in a high-paced and at times stressful environment
  • Ability to maintain productive relationships with coworkers, clients, and other contacts outside the company
  • Proficient with Microsoft Office Suite or related software
Education and Experience
  • Bachelor's degree, preferably in a scientific discipline. Preference will be given to those with an advanced degree 
  • Minimum of 10+ years previous GMP and Quality experience in the Pharmaceutical or Biotechnology industry
  • Minimum of 5+ years previous experience with qualification/validation/CSA activities in a QA or Technical capacity
  • Demonstrated experience with regulatory inspections by the FDA and EU authorities
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
  • 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:
Seran 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. Seran 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 Seran 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.
apply for this job

Apply