Senior Design Verification Engineer Med Device Delivery

AbbVie Inc.; Chicago (IL); On-site; USD 120,000 - 170,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k) with company match

Short-term incentive programs

Job summary

AbbVie's Combination Product Development & Drug Delivery Team is seeking a Senior Scientist I, Engineering – Design Verification Engineer to advance drug/device combination products. You will work on lab verification, qualification, and cross-functional validation, applying GMP/GDP practices and robust data analysis to ensure compliant, reliable test methods.

You will lead protocol development, test execution, and results reporting while collaborating with Quality, Regulatory Affairs, Clinical,

Qualifications

• Bachelor’s or higher in Mechanical or Biomedical Engineering with extensive related experience.
• 3+ years in medical device or combination products with design control knowledge.
• Familiarity with GMP, GDP, FDA regulations, and ISO standards.

Responsibilities

• Serve as SME on lab capabilities for Design Verification testing.
• Lead qualification, SOPs, and instructional training for operators.
• Develop, execute, and document design verification protocols and tests.
• Analyze data, run statistics, and present results to teams.
• Use SolidWorks and bench equipment to verify test methods.
• Collaborate across Quality, Regulatory Affairs, Clinical, and global partners.

Skills

Lab capabilities

GMP/Non-GMP equipment

Data analysis

Cross-functional teamwork

Test method development

Equipment qualification

Statistical methods

Problem solving

Education

Bachelor’s in Mechanical or Biomedical Engineering

Master’s or PhD (advantage)

Tools

SolidWorks

3D printing

Universal Test Machine (UTM)

Zwick

ELN (Polarian)

MiniTab

Job description

AbbVie's Combination Product Development & Drug Delivery Team is seeking a Senior Scientist I, Engineering – Design Verification Engineer to advance drug/device combination products. You will work on lab verification, qualification, and cross-functional validation, applying GMP/GDP practices and robust data analysis to ensure compliant, reliable test methods.

You will lead protocol development, test execution, and results reporting while collaborating with Quality, Regulatory Affairs, Clinical,