On-Site Clinical Systems Specialist: LIS & Lab Automation

Interpath Laboratory, Inc; Umatilla (OR); On-site; USD 70,000 - 100,000; Full time

Job summary

Interpath Laboratory, Inc. in Pendleton, OR, seeks a Clinical Systems Specialist to support LIS and related enterprise clinical applications. You will design, implement, and maintain configurations, instrument interfaces, and quality assurance tools while aligning with CAP standards.

The role requires a clinical laboratory background with software acumen, collaboration with end users and vendors, and a proactive approach to workflow optimization and regulatory compliance.

Qualifications

• Associate degree required; 2+ years clinical laboratory experience.
• Knowledge of medical laboratory instrumentation operation and configuration.
• ASCP or AMT Certification as MLS or MLT preferred; Bachelor’s degree encouraged.

Responsibilities

• Design, implement, and maintain configurations in the LIS and related enterprise clinical laboratory applications while ensuring quality outcomes.
• Design, implement, and maintain instrument interfaces in DI Instrument Manager and LIS.
• Design, implement, and maintain configurations on the laboratory automation line and laboratory quality assurance applications.
• Validate, document, and perform workflow assessments and impact analysis.
• Capture business needs and analyze internal systems to determine requirements for optimal utilization of applications.
• Maintain documentation to ensure compliance with CAP standards.

Skills

LIS configurations

SQL

Cross-functional collaboration

Education

Associate degree

Bachelor's degree

Tools

LIS (Laboratory Information System)

Data Innovations Instrument Manager

Cache ObjectScript

SQL tooling

Job description

Interpath Laboratory, Inc. in Pendleton, OR, seeks a Clinical Systems Specialist to support LIS and related enterprise clinical applications. You will design, implement, and maintain configurations, instrument interfaces, and quality assurance tools while aligning with CAP standards.

The role requires a clinical laboratory background with software acumen, collaboration with end users and vendors, and a proactive approach to workflow optimization and regulatory compliance.