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Associate Engineer

Abbott Laboratories

Company : Abbott Laboratories

Location : Buffalo Grove, IL, 60089

Posted Date : 28 October 2025

Job Details

Data Analyst

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 Data Analyst will be an individual contributor that works under limited supervision. You will apply data subject matter knowledge to the area of Pharmaceutical/Biological processes.

What You'll Work On:

  • Translates requirements into new solutions - Develops requirements and specifications for new and existing engineering designs.
  • Design - Proposes designs, implements or assesses designs and verifies parts or components for low complexity solutions.
  • Develops Simulations & Prototypes - Develops simulations or prototypes for new / modified designs and performs engineering analysis and testing.
  • Implements the design of new products and/or product improvements - Implements the design for parts or components and ensures designs meet established requirements.
  • Responsible for updating / creating detailed design specifications.
  • Verifies Solution - Responsible for integration, protocol development and verification of designs.
  • Documenting and Managing Change - Justifies changes, quality and regulatory information, and manufacturing readiness information.
  • Completes change documentation to include technical rationale and formal verification test results.
  • Advances Engineering Expertise - Maintains current technical skills and functional area expertise.
  • Anticipates and/or Develops/Applies Risk Mitigation - Reviews engineering technical risks and take appropriate action. Provides input into risk management documentation including FMEA and risk analyses.
  • Collaborates across functional areas - Exchanges information with product team members, scientists, engineers, and other systems development personnel.
  • Ensures quality through design Techniques and Design Alternatives - Participates in Engineering Design Reviews utilizing Engineering Procedures and Engineering Tools and incorporates recommendations.
  • Performs Investigations - Participates in investigations to determine root cause for low complexity issues.
  • Arrives at timely conclusions.
  • Maintains adherence to the Quality System - Implements and maintains the effectiveness of the quality system. Follows functional area policies and procedures.
  • Utilizes appropriate experimental, statistical and engineering tools.
  • Obtains Customer Feedback for new and/or Improve Products - Gathers inputs from internal sources and from members of the project's cross functional team to help meet product needs.
  • Selects, builds and maintain Third Party Manufacturer (TPM) product and partner relationship - For Third Party Manufactured products, assesses the assigned part / component or subsystem ability to meet corresponding requirements.
  • Strategic Orientation - Ensures activities are focused on team priorities.
  • Works with cross functional team in collaborative environment.

Required Qualifications:

  • Bachelor's degree required
  • Applies engineering technical knowledge for specified engineering discipline.

Preferred Qualifications:

  • Previous internships assignment(s)
  • Knowledge of regulations and standards affecting IVDs and biologics is desired.

The base pay for this position is $54,000.00 $108,000.00. In specific locations, the pay range may vary from the range posted.

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