Quality and Compliance Systems Specialist

Interpath Laboratory; Pendleton (OR); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

AI-driven innovation encouraged

Quality leadership role

Job summary

Interpath Laboratory is seeking a Laboratory Quality and Compliance Specialist at its Pendleton headquarters. You will lead quality assurance programs, manage regulatory compliance, and utilize innovative AI tools to enhance quality systems.

The ideal candidate has a Bachelor's degree and 3+ years in a clinical lab. Responsibilities include conducting internal audits and proficiency testing, ensuring adherence to CLIA and CAP standards, and collaborating with clinical staff on compliance initiatives.

Qualifications

• Minimum 3 years in a CLIA-regulated clinical laboratory environment.
• Experience in laboratory QA, compliance, or accreditation activities is preferred.
• ASCP certification or laboratory quality certification is a plus.

Responsibilities

• Lead quality assurance and regulatory compliance programs at the laboratory.
• Administer proficiency testing programs and implement automation solutions.
• Conduct internal audits and prepare for regulatory inspections.

Skills

Analytical skills

Communication skills

Regulatory compliance knowledge

Proficiency in Microsoft Office

Education

Bachelor's degree in Medical Laboratory Science or related field

Tools

Laboratory information systems

Document automation tools

Job description

Quality and Compliance Systems Specialist

Pendleton, OR

Laboratory Quality and Compliance Specialist

Interpath Laboratory | Pendleton, Oregon

About the Role

Interpath Laboratory is seeking a Laboratory Quality and Compliance Specialist to lead quality assurance and regulatory compliance programs at our headquarters laboratory. You'll independently manage proficiency testing, monitor quality control performance, and ensure adherence to CLIA, CAP, and state regulations.

This role offers genuine autonomy: you'll interpret regulatory requirements, scope internal audits, evaluate root causes, and formulate corrective actions. You'll also champion the innovative use of AI tools and automation to strengthen our quality systems, reduce manual effort, and enhance compliance readiness.

What You’ll Do

• Administer proficiency testing programs across all regulated analytes and specialties
• Design and implement automation solutions that reduce manual work while preserving regulatory integrity
• Analyze QC and PT data, identify trends, and track corrective actions to completion
• Conduct internal audits and prepare for regulatory inspections (CMS, CAP, state agencies)
• Investigate deviations and complaints; determine root causes and implement preventive measures
• Maintain current knowledge of CLIA, CAP, FDA, OSHA, HIPAA, and state regulations
• Support method validation and verification activities
• Leverage AI resources to audit documentation, analyze data, and identify compliance risks proactively
• Collaborate with laboratory leadership and clinical systems staff on quality and compliance initiatives

Who You Are

Required Qualifications

• Bachelor's degree in Medical Laboratory Science, Clinical Laboratory Science, Biology, Chemistry, or related field
• Minimum 3 years in a CLIA-regulated clinical laboratory environment
• Valid driver's license

Preferred Qualifications

• 2+ years in laboratory QA, compliance, or accreditation activities
• Experience with AI tools (LLMs, document automation, data analysis platforms)
• Laboratory information systems, middleware, or instrument interface experience
• Method validation and statistical QC expertise (Levey-Jennings, Westgard rules)
• ASCP certification (MLS, MLT, CLS) or laboratory quality certification (ASQ CQA, ASCP QLC)
• Experience supporting laboratory inspections or accreditation surveys

Core Competencies

• Strong analytical and communication skills
• Ability to manage multiple priorities and work independently
• Proficiency in Microsoft Office and document control systems
• Sound judgment in regulated environments

Physical Requirements

• Ability to sit, stand, and walk for extended periods throughout the workday.
• Ability to use a computer, keyboard, mouse, and standard office equipment for extended periods, including repetitive hand and wrist motion.
• Ability to lift, carry, push, or pull up to 25 pounds occasionally (e.g., proficiency testing shipments, supplies, reference materials).
• Ability to perform close visual work, including reading small print on laboratory documentation, instrument displays, and computer screens.
• Ability to communicate clearly in person, by telephone, and through electronic platforms.
• Ability to travel by automobile or commercial transportation to other Interpath Laboratory sites as assigned.

What We Offer

A role where quality leadership matters and AI-driven innovation is encouraged. Based at our headquarters laboratory in Pendleton with occasional travel to other sites.

Equal Employment Opportunity

As set forth in Interpath Laboratory’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.