Process Engineer

Pfizer; Dayton (OH); On-site; USD 90,000 - 120,000; Full time

Job summary

Pfizer in Dayton, OH is seeking a Process Engineer to support plant operations and develop solutions for production and facilities challenges. You will manage smaller engineering projects and coordinate with project engineering on larger initiatives.

The role requires a Bachelor's degree in chemical or mechanical engineering and at least 3 years of process engineering or project management experience in a GMP environment. Proficiency in MS Office and MS Project or Smartsheet is expected.

Qualifications

• Bachelor's degree in chemical or mechanical engineering or related field.
• At least 3 years of process engineering or project management experience.
• Experience in a pharmaceutical or regulated GMP environment with CAPA and deviations.

Responsibilities

• Review operations and identify process improvements related to productivity, efficiency, and safety.
• Develop engineering solutions and investigate alternative technologies.
• Define project requirements, scope, technical designs, cost justifications, and approval documentation.
• Manage project schedules, costs, contractors, procurement, quality control, and scope changes.
• Prepare or review process design documents, calculations, drawings, and specifications.
• Coordinate project startup, validation, regulatory, documentation, and closeout activities.

Skills

Process engineering

Project management

Regulatory compliance

Education

Bachelor's degree in chemical or mechanical engineering

Tools

MS Project

Smartsheet

MS Office

AutoCAD

Job description

Role overview:

Our client is seeking a Process Engineer to support plant operations and develop solutions to production and facilities challenges. You will also manage smaller engineering projects and coordinate with project engineering on larger initiatives.

Key responsibilities:

• Review operations and identify process improvements related to productivity, efficiency, and safety.
• Develop engineering solutions and investigate alternative technologies.
• Define project requirements, scope, technical designs, cost justifications, and approval documentation.
• Manage project schedules, costs, contractors, procurement, quality control, and scope changes.
• Prepare or review process design documents, calculations, drawings, and specifications.
• Coordinate project startup, validation, regulatory, documentation, and closeout activities.
• Bachelor’s degree in chemical engineering, mechanical engineering, or a related engineering discipline.
• At least 3 years of process engineering or project management experience.
• Experience in a pharmaceutical or regulated GMP environment, including CAPA and deviations.
• Proficiency with Microsoft Office and MS Project or Smartsheet.

Preferred qualifications:

• Experience with stable isotopes or AutoCAD.
• Chemical or life sciences background.
• Advanced engineering skills, including gas distillation design and optimization.
• Ability to interpret and apply policies, codes, standards, and regulations.