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Imaging Quality Control Specialist Jobs (NOW HIRING)

Quality Control Specialist - Portland, Oregon (OR) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Quality Control Specialist - Korean Speaking Pay: Starting at $18.00 per hour, with higher starting pay available based on experience Position Type: Full-Time Job Summary We are seeking a dependable ...

Quality Control Specialist

Wichita, KS ยท On-site

$80 - $100/hr

Quality Control Specialist Wichita, Kansas Do you enjoy ensuring designs meet specified standards? Do you like to be on teams that provide lasting infrastructure? Do you like to exceed client ...

Quality Control Specialist - Portland, Oregon (OR) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Quality Control Specialist

Tempe, AZ ยท On-site

$19 - $21/hr

Quality Control Specialist Department: Quality Assurance Reports To: Quality Control Manager FSLA Status: Non-Exempt Employment Type: Full-Time / In-House Job Summary: The Quality Control Specialist ...

$65 - $90/hr

We offer flexible schedules and remote opportunities MERIT is seeking a full-time position to fluently performs the duties of the Imaging Quality Control Specialist (IQCS) I role as well as creating ...

New

$60 - $90/hr

We offer flexible schedules and remote opportunities MERIT is seeking a full-time position to fluently performs the duties of the Imaging Quality Control Specialist (IQCS) I role as well as creating ...

New

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Imaging Quality Control Specialist information

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How much do imaging quality control specialist jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for imaging quality control specialist in the United States is $28.64, according to ZipRecruiter salary data. Most workers in this role earn between $19.95 and $35.58 per hour, depending on experience, location, and employer.

What is an imaging quality control specialist?

Imaging Quality Control Specialists are professionals who ensure that medical images, such as X-rays, MRIs, and CT scans, meet quality standards for clarity, accuracy, and diagnostic value. They inspect and test imaging equipment, review images for technical quality, and ensure that protocols and regulatory guidelines are followed. Their work helps healthcare providers make accurate diagnoses and maintain patient safety by minimizing errors related to poor image quality. These specialists often collaborate with radiologists, technologists, and equipment manufacturers to resolve issues and implement improvements.

What are the key skills and qualifications needed to thrive as an imaging quality control specialist?

To thrive as an Imaging Quality Control Specialist, you need a solid background in radiologic technology, image analysis, and quality assurance, often supported by a degree in medical imaging or a related field. Familiarity with imaging modalities (such as MRI, CT, and X-ray), picture archiving and communication systems (PACS), and relevant quality control protocols and certifications like ARRT or CQIA is typically required. Attention to detail, strong analytical skills, and effective communication help specialists identify issues and collaborate with technologists and radiologists. These skills are crucial for ensuring diagnostic image accuracy, patient safety, and compliance with regulatory standards.

What are some common challenges imaging quality control specialists face when ensuring consistent image quality across different equipment and modalities?

Imaging Quality Control Specialists often encounter challenges such as variability in imaging equipment performance, maintaining calibration standards across multiple modalities, and adapting to updates in imaging technology. They must meticulously track and interpret quality metrics, troubleshoot discrepancies, and ensure compliance with regulatory standards. Regular collaboration with radiologists, technologists, and equipment vendors is essential to resolve issues quickly and maintain high-quality diagnostic images in a fast-paced healthcare environment.

What is the difference between Imaging Quality Control Specialist vs Radiologic Technologist?

AspectImaging Quality Control SpecialistRadiologic Technologist
CredentialsCertification in imaging quality or related fields, sometimes requiring ARRT or equivalentARRT certification or state licensure in radiography
Work EnvironmentMedical imaging departments, quality assurance labs, healthcare facilitiesHospitals, clinics, diagnostic imaging centers
Primary FocusEnsuring imaging equipment produces high-quality images, maintaining standardsPerforming diagnostic imaging procedures on patients
Common UsageQuality control, equipment calibration, image optimizationPatient positioning, image capturing, radiation safety

The main difference is that Imaging Quality Control Specialists focus on maintaining imaging standards and equipment quality, while Radiologic Technologists perform diagnostic imaging procedures on patients. Both roles require certification and work in healthcare settings, but their core responsibilities differ significantly.

More about Imaging Quality Control Specialist jobs

What cities are hiring for Imaging Quality Control Specialist jobs?

Cities with the most Imaging Quality Control Specialist job openings:

What states have the most Imaging Quality Control Specialist jobs?

States with the most job openings for Imaging Quality Control Specialist jobs include:

Infographic showing various Imaging Quality Control Specialist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $59,574 per year, or $28.6 per hour.

Quality Control Specialist

ICON

Portland, OR โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 6 days ago


Job description

Quality Control Specialist - Portland, Oregon (OR)
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
Quality Control Specialist
Position Overview
The Quality Control Specialist plays a critical role in ensuring the accuracy, integrity, and compliance of laboratory data, documentation, and quality records. This position performs quality control reviews of study-related data and laboratory documentation, supports quality systems and document control processes, monitors laboratory quality metrics, and contributes to continuous improvement initiatives. The ideal candidate is highly detail-oriented, analytical, and committed to maintaining the highest standards of quality and regulatory compliance within a regulated laboratory environment.
Position Summary
The Quality Control Specialist is responsible for the review, verification, and maintenance of laboratory data, documentation, and quality records in accordance with established Standard Operating Procedures (SOPs), study protocols, analytical methods, and regulatory requirements. This role collaborates cross-functionally to ensure data integrity, compliance, and consistency across laboratory operations while supporting quality systems, laboratory metrics reporting, document control initiatives, and continuous improvement efforts.
The Quality Control Specialist contributes to departmental objectives by working independently, managing multiple priorities, completing assigned projects within established timelines, and maintaining effective communication with internal stakeholders.
Core Values & Behaviors
  • Recognize, exemplify, and adhere to ICON's values centered on People, Clients, and Performance.
  • Embrace and contribute to a culture of continuous improvement focused on enhancing efficiency, quality, compliance, and customer satisfaction.
  • Demonstrate a strong commitment to quality, accuracy, integrity, and regulatory compliance.
  • Collaborate effectively within a team environment and contribute to departmental and organizational goals.
  • Communicate professionally and effectively with supervisors, colleagues, Project Leaders, Project Managers, and cross-functional teams.
  • Prioritize workload effectively and manage time to meet deadlines.
  • Maintain punctual and reliable attendance in accordance with company policy.
  • Adhere to all safety procedures and maintain a safe working environment.

Key Responsibilities
Data Review & Compliance
  • Perform quality control (QC) review of study participant results and laboratory run packets to ensure accuracy, completeness, and compliance with applicable SOPs, protocols, and regulatory requirements.
  • Conduct review of Biomarker Reports and supporting study documentation to verify data accuracy and integrity.
  • Perform QC review of validation documentation and associated records.
  • Review methods, reports, study data, and supporting documentation for accuracy, consistency, completeness, and proper formatting.
  • Identify, document, and communicate data discrepancies, quality issues, and compliance concerns in a timely manner.
  • Assist with investigations and resolution of data and documentation discrepancies to support study integrity and quality objectives.
  • Provide backup support for Incoming Materials review activities and QC review of Production Batch Records.
  • Read, understand, and comply with SOPs, safety requirements, regulatory guidelines, and company policies.
Documentation & Records Management
  • Maintain accurate, complete, and audit-ready records in accordance with regulatory, client, and company requirements.
  • Support document control activities, including the creation, review, revision, maintenance, and archival of controlled documentation.
  • Develop and support improvements to document control processes to enhance compliance, organization, efficiency, and traceability.
  • Compile laboratory notebooks, departmental records, and supporting documentation for archival and regulatory compliance.
  • Ensure documentation practices remain consistent, accurate, organized, and inspection-ready.

Quality Systems & Continuous Improvement
  • Compile, maintain, analyze, and report laboratory quality metrics and key performance indicators.
  • Develop and maintain tracking tools related to quality events, deviations, errors, and laboratory trends.
  • Identify opportunities for process improvement through trend analysis, quality assessments, and operational observations.
  • Support continuous improvement initiatives focused on quality systems, documentation practices, compliance, and operational efficiency.
  • Respond to Quality Assurance observations and assist with corrective and preventive actions (CAPAs) as required.
  • Participate in sponsor audits, regulatory inspections, and quality assessments as needed.

Cross-Functional Support
  • Collaborate with laboratory, operations, project management, and quality teams to ensure timely completion of quality review activities.
  • Support departmental projects and initiatives aimed at improving compliance, consistency, and overall laboratory performance.
  • Perform additional duties as assigned by management.
  • Participate in training and professional development activities to maintain knowledge of industry regulations and best practices.

Qualifications & Experience
Required Qualifications
  • Minimum of five (5) years of laboratory experience in a regulated environment.
  • Working knowledge of GxP regulations and applicable industry guidance documents.
  • Proficiency with Microsoft Office Suite applications.
  • Experience utilizing laboratory instrument data systems.
  • Strong attention to detail and commitment to data integrity.
  • Excellent organizational, communication, and problem-solving skills.
  • Ability to work independently while collaborating effectively across multiple departments.
Preferred Qualifications
  • Experience using JMP statistical software for data analysis, trending, reporting, and visualization of laboratory quality metrics.
  • Experience supporting sponsor audits, regulatory inspections, and quality assessments.
  • Knowledge of laboratory quality systems, document control processes, data integrity requirements, and Good Documentation Practices (GDP).
  • Experience analyzing quality metrics, deviations, investigations, CAPAs, and laboratory performance trends.
  • Experience performing quality control reviews of scientific data, validation documentation, reports, and regulated laboratory records.
  • Experience working within a pharmaceutical, biotechnology, contract research organization (CRO), or other regulated laboratory environment.
  • Demonstrated ability to identify process improvement opportunities and contribute to continuous improvement initiatives.
  • Experience collaborating cross-functionally with laboratory operations, Quality Assurance, Project Management, and other technical stakeholders.

Working Conditions
  • Primarily laboratory and office-based work environment.
  • Extended periods of computer-based work and document review.
  • Ability to manage multiple priorities and deadlines in a regulated environment.
  • May participate in audits, inspections, and cross-functional project activities as required.

#LI-HD1
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply