Senior Scientist, Lab Automation & Process Dev

Abbott Laboratories; Madison (WI); On-site; USD 78,000 - 156,000; Full time

Job summary

Abbott Laboratories in Madison, WI seeks a Product Development and Automation Senior Scientist to support automation, IT, and software systems in the clinical laboratory. The role includes UAT, validation, and collaboration with LIS developers to improve test systems and workflow.

You will work autonomously on moderately complex projects, mentor junior staff, and ensure regulatory compliance with FDA, CLIA, and CAP. Strong English communication and ability to lead design reviews are required.

Qualifications

• Bachelor’s Degree in Clinical Laboratory Science, Medical Technology, or a relevant field.
• 6+ years of relevant work experience in a clinical laboratory.
• 1+ years of work experience with LIS configuration and UAT verification.
• Authorization to work in the United States without sponsorship.

Responsibilities

• Assist in UAT testing.
• Edit and review controlled documents within the laboratory document control system to support changes or implementation of software and process changes.
• Develops process architectures and functional specifications based on user and workflow requirements; leads planning activities and conducts complex design, testing, or performance evaluations.
• Accurately estimates task effort, including work by others.
• Maintain all records and follow procedures to meet regulatory requirements such as FDA, CLIA, and CAP.

Skills

UAT testing

LIS configuration

Analytical testing

Project leadership

Documentation

Education

Bachelor's in Clinical Laboratory Science / Medical Technology

Tools

LIS/LIMS

Job description

Abbott Laboratories in Madison, WI seeks a Product Development and Automation Senior Scientist to support automation, IT, and software systems in the clinical laboratory. The role includes UAT, validation, and collaboration with LIS developers to improve test systems and workflow.

You will work autonomously on moderately complex projects, mentor junior staff, and ensure regulatory compliance with FDA, CLIA, and CAP. Strong English communication and ability to lead design reviews are required.