Senior Principal Process Engineer — Pharma Manufacturing

AbbVie Inc.; North Chicago (IL); Presencial; USD 120.000 - 180.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Paid time off

Medical/dental/vision insurance

401(k) plan

Descripción de la vacante

AbbVie Inc. in North Chicago, IL seeks a senior engineer to lead technical workstreams across the lifecycle, collaborating with cross‑functional partners to implement robust manufacturing solutions.

You will design site-level processes, lead optimization efforts, validate processes, and document standards. Strong leadership and program management are essential to drive projects to completion and ensure compliance.

Formación

• Bachelor’s degree in engineering (Mechanical, Electrical, Chemical) required.
• 8+ years’ experience in the pharmaceutical industry formulation.
• Knowledge of Engineering standards.
• Demonstrated leadership and team building skills.
• Strong problem-solving abilities.
• Proven track record of managing projects through to completion.
• Excellent communication skills with layers of management.

Responsabilidades

• Leads site-level process designs by defining operating ranges and acceptance criteria.
• Drives process improvement and optimization workstreams and documents results.
• Conducts process validation and troubleshooting of manufacturing processes.
• Establishes technical standards for process documentation and change execution.
• Guides engineers through technical decisions and tracks actions to closure.
• Delivers high-quality technical outputs and communicates progress to stakeholders.

Conocimientos

Bachelor’s degree in engineering

8+ years’ pharmaceutical experience

Engineering standards

Leadership and team building

Problem-solving abilities

Project management

Communication with management levels

Educación

Bachelor’s degree in engineering (Mechanical, Electrical, Chemical)

Descripción del empleo

AbbVie Inc. in North Chicago, IL seeks a senior engineer to lead technical workstreams across the lifecycle, collaborating with cross‑functional partners to implement robust manufacturing solutions.

You will design site-level processes, lead optimization efforts, validate processes, and document standards. Strong leadership and program management are essential to drive projects to completion and ensure compliance.