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Job Description
📋 Description
- An engineering/analyst professional who applies engineering/scientific knowledge to basic
- Support compliance with EH&S, AbbVie Engineering Standards, and governance; identify compliance
- Define project scope with stakeholders; plan and manage multiple tasks; assist in economic analysis
- Plan and conduct small projects; coordinate qualification activities (EFU, cleaning validation)
- Design and improve products/processes/equipment; communicate findings and recommendations to
- Build relationships with teams, customers, contractors, and vendors; convey information effectively
🎯 Requirements
- Bachelor’s degree in Mechanical, Chemical, Electrical, Process, Biomedical, or related Engineering
- 0-2 years engineering experience in pharmaceutical/ GMP environment preferred.
- Understanding of biopharma manufacturing processes and cGMP regulatory requirements (FDA/EMA, data
- Familiarity with capital project execution, equipment installation, commissioning, startup support
- Knowledge of process equipment/utilities (CIP, SIP, PW, WFI, clean steam, gases) and
- Strong problem-solving, communication, and cross-functional collaboration skills; continuous
🎁 Benefits
- AbbVie offers comprehensive benefits including PTO, medical/dental/vision, 401(k).
- Eligible for short-term incentive programs; equal opportunity employer.