Staff Systems Integration Specialist

Abbott; Illinois; On-site; USD 87,000 - 173,000; Full time

Benefits offered by this job

Medical coverage

Retirement plan

Tuition reimbursement

FreeU education benefit

Job summary

Abbott Park, IL-based Diagnostics/Core Lab is seeking a Staff Systems Integration Specialist for on-site work. You will define system requirements, execute integration testing, and drive data-based improvements across hardware, software, and assays.

Lead risk management activities, mentor teammates, and ensure quality system compliance while meeting project timelines. Abbott offers extensive benefits and growth opportunities.

Qualifications

• Bachelor’s degree in Life or Physical Science, Bioengineering, Biomedical Engineering or closely related discipline.
• Minimum 7 years of experience leading complex system and risk analysis.
• Demonstrated ability to lead, analyze data, and influence stakeholders.

Responsibilities

• Define and document system requirements across hardware, software, assays, reagents, and labeling.
• Develop and execute integration, verification, and validation testing.
• Analyze data, interpret results, and propose product/process improvements.
• Maintain assay files with accuracy for new launches and changes.
• Lead risk management activities including FMEA and hazard assessments.
• Mentor team members and collaborate across engineering, quality, and operations.

Skills

Data-driven decision making

Stakeholder influence

Systems thinking

Creativity and independence

Quality systems knowledge

Education

Bachelor’s degree in Life or Physical Science, Bioengineering, Biomedical Engineering

Tools

DOORS

APLM

SBM

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to :

• Career development with an international company where you can grow the career you dream of.
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with a high employer contribution.
• Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
• A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity :

Our Diagnostics / Core Lab business currently has a full-time, on-site opportunity for a Staff Systems Integration Specialist.

This position will be based at our Abbott Park, IL office. Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe. The crucial information derived from our tests, instruments, and informatics systems is often the first step in patient care decision-making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers.

What You’ll Work On

• Ensure compliance with quality and regulatory requirements while supporting continuous improvement efforts.
• Define and document system requirements across hardware, software, assays, reagents, and labeling to ensure products perform as intended.
• Develop and execute integration, verification, and validation testing to assess overall system performance and reliability.
• Analyze technical data, interpret results, and recommend improvements to product performance, quality, and manufacturing processes.
• Create, review, and maintain assay files, ensuring accuracy and compliance for new product launches and product changes.
• Support risk management activities, including FMEA reviews, hazard assessments, and performance optimization studies.
• Document testing, investigations, and engineering activities to meet quality system and design control requirements.
• Mentor team members, share technical expertise, and collaborate across engineering, scientific, quality, and operations teams.
• Manage multiple projects, maintain organized records, and consistently meet project timelines.
• Drive data-based decision-making using statistical analysis, experimental design, and performance metrics.
• Leads development of systems integration test methods / processes and troubleshooting instrument (hardware/software/and assay/reagent interaction issues to determine root cause and possible solutions. Resolves complex system-level problems.
• Leads team members in application and analysis of multiple optimization process techniques : Set targets, ranges, and specs – DOE, Guard band, Capability (CPk), Test Method development, troubleshoot parts and subsystems. Reviews and / or develop FMEA, hazards, modes of control for risk management. Leads complex investigations involving interacting system level issues.
• Responsible for implementing and maintaining the effectiveness of the quality system.
• Proficiency in assay file parameters review and the assay file management system.

Required Qualifications

• Bachelor’s degree in Life or Physical Science, Bioengineering, Biomedical Engineering, or closely related discipline is preferred.
• Minimum 7 years
• Recognized experience leading complex system and risk analysis
• Demonstrated ability to lead and utilize data to make decisions and influence stakeholders
• Demonstrated success in technical proficiency, creativity, and independent thought.
• Demonstrated ability to apply principles of systems thinking to accelerate performance
• Expert knowledge of systems and/or assay development principles and concepts
• Knowledge of Product Risk Management Best Practices and Tools
• Demonstrated Customer Focus, making their needs a primary focus of one’s actions

Preferred Qualifications

• Systems integration experience in Clinical Chemistry and / or Immuno Assay
• Experience in Clinical Chemistry, immunoassay development, assay technical support or assay reagent design.
• Demonstrated Customer Focus, making their needs a primary focus of one’s actions.
• Knowledge of regulations and standards affecting IVDs and Biologics.
• Demonstrates use of statistics, design of experimentation, DOORS, APLM, SBM and
• Comfortable working with technical data, test methods, and regulated product development processes.

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives :

https ://abbottbenefits.com/

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at abbott.com, on LinkedIn at https ://www.linkedin.com/company/abbott-/, and on Facebook at https ://www.facebook.com/AbbottCareers.

The base pay for this position is $86,700.00 – $173,300.00. In specific locations, the pay range may vary from the range posted.