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Project Engineer, Site Strategy and Portfolio

AbbVie

North Chicago, ILOnsitePosted 1 day agoUSD 65500 - USD 125500 yearly
Full TimeEntry LevelProgram / Project ManagementPharmaceutical
Original posting ↗

Summary

As Project Engineer, Site Strategy and Portfolio at AP16 Lake County, you support the Associate Director, Business Excellence in running the processes through which the site plans its future: the site programme portfolio, the Long-Range Plan (LRP) and Annual Plan inputs, and the Site Master Plan, which brings footprint, capacity, capital and people capabilities into a single multi-year view.

Job description

Responsibilities

  • Portfolio tracking: Maintain a single, current view of all site programs and projects: status, milestones, resourcing and interdependencies. Work with program leads to keep data accurate and complete.
  • Portfolio review support: Prepare the package for the site portfolio review, document decisions and actions, and follow actions through to closure with their owners.
  • Portfolio standard and templates: Maintain the site's program management templates (charters, integrated timelines, RACI, risk registers, close-out) and help program leads apply them. Check stage-gate documentation for completeness ahead of reviews.
  • Status evidence and early warning: Compare program progress against plan and flag deviations, emerging risks and overdue deliverables to the Associate Director early, with the supporting data.
  • LRP and Annual Plan coordination: Coordinate the site calendar and templates for LRP, LBE and Annual Plan inputs; collect and consolidate functional inputs and reconcile them with Finance.
  • Site Master Plan models and tools: Build and maintain the models and tools behind the Site Master Plan, covering capacity, footprint, utilities, capital and people capabilities, and keep the underlying data current.
  • Site Master Plan support: Gather inputs from functional teams, prepare materials for planning sessions, and identify gaps, inconsistencies and sequencing issues for discussion.
  • Site strategy analysis: Provide analysis, benchmarking and well-structured documents and presentations to support the site strategy and the functional strategies aligned with it, including people and capability planning with HR.
  • Transformation support: Track milestones, risks and interdependencies of site transformation programs, and coordinate assigned tasks within transformation workstreams.
  • Reporting and continuous improvement: Build and maintain portfolio dashboards, automate recurring reporting where possible, and propose improvements to the site's planning and governance practices.

Qualifications

  • Bachelor's degree in engineering (e.g. mechanical, chemical, industrial or related discipline) required.
  • 2–4 years of professional experience.
  • Internships or co-ops in manufacturing, engineering or operations preferred; regulated industry (pharma, biotech, medical device, food) a plus.
  • Exposure to project management through coursework, internships or early roles.
  • CAPM or Lean / Six Sigma Yellow or Green Belt a plus.
  • Strong analytical skills, including building models and working with data in MS Excel.
  • Power BI, Smartsheet or MS Project a plus.
  • Clear, structured written communication and the ability to build effective PowerPoint materials.
  • Highly organized, with strong attention to detail and reliable follow-through on actions and deadlines.
  • Confidence working with experienced colleagues and senior stakeholders; willingness to ask questions and raise issues early.
  • Basic understanding of GMP and EHS principles, or the ability to learn them quickly.
  • Genuine interest in manufacturing operations, capacity planning and site strategy.
  • Eagerness to learn and to take on progressively broader responsibility.

Requirements

  • Bachelor's degree in engineering (e.g. mechanical, chemical, industrial or related discipline) required
  • 2–4 years of professional experience
  • Exposure to project management through coursework, internships or early roles
  • Strong analytical skills, including building models and working with data in MS Excel
  • Clear, structured written communication and the ability to build effective PowerPoint materials
  • Highly organized, with strong attention to detail and reliable follow-through on actions and deadlines
  • Confidence working with experienced colleagues and senior stakeholders
  • Basic understanding of GMP and EHS principles, or the ability to learn them quickly
  • Genuine interest in manufacturing operations, capacity planning and site strategy

Benefits

  • Paid time off
  • Medical, Dental & Vision
  • 401(k)
  • Short-term incentive programs

Company overview

AbbVie is a global biopharmaceutical company that discovers, develops, and markets advanced therapies for some of the world's most complex and serious diseases. Founded in 2013 as a spin-off from Abbott Laboratories, AbbVie has established itself as a leader in immunology, oncology, neuroscience, eye care, and virology. The company's flagship product, Humira (adalimumab), was one of the world's top-selling drugs for treating autoimmune conditions like rheumatoid arthritis and Crohn's disease. AbbVie maintains a robust pipeline of innovative medicines and has expanded its portfolio through strategic acquisitions, including Allergan in 2020. With research facilities across the United States and globally, AbbVie focuses on advancing science to improve patient outcomes while maintaining strong commercial operations worldwide. The company operates with a patient-centric approach and invests significantly in research and development to address unmet medical needs across multiple therapeutic areas.

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