Associate, Engineer
AbbVie · North Chicago, IL
OtherFull timeCompany career page
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Role summary
Early-career engineering professional supporting research and development at a biopharmaceutical manufacturing site. The role involves executing engineering projects, performing technical analyses, and ensuring compliance with regulatory standards in GMP environments.
What they're looking for
- Bachelor's degree in Mechanical, Chemical, Electrical, Process, Biomedical, or related Engineering
- 0-2 years engineering experience in pharmaceutical or GMP manufacturing preferred
- Knowledge of cGMP regulations, FDA, EMA, and data integrity requirements
- Understanding of Commissioning, Qualification, and Validation (CQV) protocols and documentation
- Strong technical problem-solving and root cause analysis capabilities
- Proficiency in Microsoft Office and familiarity with SAP, CMMS, or AutoCAD
- Excellent written and verbal communication skills for cross-functional collaboration
What you'll be doing
- Plan and execute small to mid-sized engineering projects with conventional methods and equipment
- Support qualification activities, cleaning validation, and prototype testing with documentation
- Investigate technical issues, conduct tests, gather data, and recommend engineering solutions
- Assist in training personnel on facility, process, and equipment operations
- Review existing designs and create proposals applying standard engineering principles
Privacy & handoff
This role links to AbbVie's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.