Senior Pharma Facilities & Critical Systems Engineer

BAXTER

Peoria (IL)

In loco

USD 152.000 - 209.000

Tempo pieno

14 giorni+

Una candidatura completa in un minuto

Curriculum e lettera di presentazione personalizzati, pronti da inviare.

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Vantaggi offerti da questo lavoro

Healthcare and dental coverage fromDay
401(k) with company match
Paid time off 20–35 days

Descrizione del lavoro

The Baxter Global Engineering team is seeking an Engineering Specialist, Facilities and Critical Systems, to ensure the reliability, performance, and regulatory compliance of our pharmaceutical facilities and utilities. You will lead engineering standards, evaluate designs, and drive capital projects across our global network.

You will work with site engineers and cross-functional teams, applying cGMP knowledge, and travel up to 25% to support manufacturing operations worldwide.

Competenze

  • Bachelor's degree in Mechanical Engineering or a related field.
  • 15+ years of experience in pharmaceutical facility, utility, or systems engineering.
  • 3+ years of experience supporting manufacturing operations.
  • 8+ years of experience in an engineering leadership or senior technical engineering role.
  • Experience applying cGMP requirements within a regulated manufacturing environment.
  • Knowledge of facility and utility systems, including HVAC, WFI, compressed air, mechanical, electrical, plumbing, structural, and energy management systems.
  • Knowledge of FDA, OSHA, 21 CFR, ISO, and applicable building and safety regulations.
  • Experience supporting capital projects from concept through startup and turnover.
  • Proficiency with AutoCAD, Revit, or similar engineering design tools.
  • Strong communication and problem-solving skills with the ability to work across multiple functions and locations.
  • Experience in facility design, construction management, or capital project execution.
  • Knowledge of ISPE, ASME, NFPA, EPA, and environmental health and safety requirements applicable to pharmaceutical manufacturing.
  • Experience developing engineering standards or governance programs for a global organization.
  • Experience with Lean Manufacturing, Six Sigma, TPM, or other continuous improvement methodologies.

Mansioni

  • Develop and maintain engineering standards and guidance documents for facilities, utilities, and capital projects.
  • Provide technical support and subject matter expertise for pharmaceutical facility and utility systems.
  • Review facility designs, engineering studies, and project plans to ensure alignment with company standards and regulatory expectations.
  • Support manufacturing sites in the planning and execution of facility upgrades and improvement projects.
  • Evaluate facility and utility system performance and recommend solutions to address technical issues and improve reliability.
  • Monitor changes in industry practices and regulatory requirements and recommend updates to engineering standards and procedures.
  • Develop and maintain project documentation standards, including SOWs, URSs, and BODs.
  • Participate in project gate reviews and capital planning activities.
  • Support sustainability initiatives through facility improvements, energy-efficient design practices, and carbon reduction efforts.
  • Partner with manufacturing, maintenance, purchasing, and project teams to address facility and utility-related challenges.
  • Provide technical guidance and mentorship to engineering teams across the organization.
  • Travel domestically and internationally up to 25%.

Conoscenze

Mechanical engineering knowledge
Leadership
Communication
Problem-solving

Formazione

Bachelor's degree in Mechanical Engineering or related field

Strumenti

AutoCAD
Revit

Descrizione del lavoro

The Baxter Global Engineering team is seeking an Engineering Specialist, Facilities and Critical Systems, to ensure the reliability, performance, and regulatory compliance of our pharmaceutical facilities and utilities. You will lead engineering standards, evaluate designs, and drive capital projects across our global network.

You will work with site engineers and cross-functional teams, applying cGMP knowledge, and travel up to 25% to support manufacturing operations worldwide.

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