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Qc Specialist Jobs (NOW HIRING)

ICON

Quality Control Specialist

Portland, OR · On-site

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 ...

Integra

Quality control specialist

Lanett, AL · On-site

$18/hr

Quality Control Specialist - Korean-Speaking Pay: Starting at $ 70,000- $ 90,000 per year based on experience Position Type: Full-Time Job Summary We are seeking a dependable, detail-oriented Quality ...

GARVER LLC

Quality Control Specialist

Wichita, KS · 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 ...

Icon plc

Quality Control Specialist

Portland, OR · On-site

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 ...

Branded Bills

Quality Control Specialist

Tempe, AZ · 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 ...

McGough

Quality Control Specialist

Fargo, ND · On-site

QUALITY CONTROL SPECIALIST The Quality Control (QC) Specialist supports the successful delivery of construction projects by coordinating and executing quality control activities throughout the ...

SpectronRx

QC Specialist

Indianapolis, IN · On-site

$29 - $34/hr

Quality Control Specialist COMPANY OVERVIEW SpectronRx is a growing Contract Development and Manufacturing Organization (CDMO) based in Indianapolis, Indiana, and production locations in South Bend ...

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Qc Specialist information

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$12

$28

$49

How much do qc specialist jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for qc 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 a QC Specialist?

QC Specialists, or Quality Control Specialists, are professionals responsible for ensuring that products and processes meet established quality standards. They inspect, test, and evaluate materials, components, and finished products to identify defects or deviations from specifications. QC Specialists often document their findings, collaborate with other departments to resolve quality issues, and help implement corrective actions. Their role is critical in industries such as manufacturing, pharmaceuticals, and food production to maintain product safety and customer satisfaction.

What are the key skills and qualifications needed to thrive as a QC Specialist, and why are they important?

To thrive as a QC Specialist, you need a solid background in quality control procedures, data analysis, and a relevant science or engineering degree. Familiarity with laboratory information management systems (LIMS), statistical process control (SPC) software, and knowledge of industry-specific regulations such as GMP or ISO standards are typically required. Attention to detail, problem-solving abilities, and strong communication skills help ensure accuracy and effective collaboration. These competencies are crucial for maintaining product quality, regulatory compliance, and efficient operations within quality-driven industries.

What are some common challenges a QC Specialist faces when working with cross-functional teams?

QC Specialists often collaborate closely with production, engineering, and R&D teams to ensure products meet quality standards. A common challenge is bridging communication gaps between departments, as priorities and technical language can vary. Navigating these differences requires strong interpersonal skills and the ability to clearly present quality concerns and solutions. Successful QC Specialists proactively foster positive relationships and strive for a shared commitment to product excellence.

What is the difference between Qc Specialist vs Quality Control Technician?

AspectQc SpecialistQuality Control Technician
CertificationsISO, Six Sigma, GMPISO, GMP
Work EnvironmentLaboratories, manufacturing plantsManufacturing sites, labs
ResponsibilitiesOversees quality processes, audits, documentationPerforms inspections, tests products

The Qc Specialist typically has broader responsibilities, including process oversight and audits, while the Quality Control Technician focuses on testing and inspecting products. Both roles require similar certifications and are essential in manufacturing and lab environments, but the Qc Specialist often plays a more strategic role in quality management.

Do you need a degree for a QC specialist?

A degree is often preferred for a QC specialist role, especially in industries like pharmaceuticals or manufacturing, but some positions may accept relevant work experience or technical certifications in lieu of a formal degree. Strong attention to detail, knowledge of quality standards, and familiarity with testing tools are also important qualifications for the role.
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Qc Specialist jobs near you
Infographic showing various Qc Specialist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $59,574 per year, or $28.6 per hour.

Quality Control Specialist

ICON

Portland, OR • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 8 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

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