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cGMP Consulting

cGMP compliance consulting for pharma

Senior Project Engineer - Fit & Finish

Design EngineeringConfirmed live in the last 24 hours
Full-timeMelrose Park, IL, USA$80k - $100k /yrIn-person

About the Job

Requirements

  • A bachelor's degree in technical science, engineering, or a related field is required.
  • A minimum of 5 years of engineering experience is required; pharmaceutical manufacturing industry experience is preferred.
  • Working knowledge of FDA regulations and guidance, and Good Manufacturing Practices, with attention to detail.
  • Preferred technical knowledge and understanding of statistical analysis tools and methods.
  • Experience with high-performance teams and strong interpersonal and project management skills.
  • Computer literacy in word processing, spreadsheets, project management, and PowerPoint is desired.
  • Ability to generate and modify different reports.
  • Thorough understanding of mechanical and plant systems, and ability to read construction and process drawings.
  • Ability to interact with varying levels within the company.
  • Ability to work independently and in partnership with others, use initiative and drive to achieve results, and solve complex problems.
  • Technical written and verbal communication, documentation, and organizational skills to collaborate with plant staff.
  • Demonstrated ability to troubleshoot equipment using analytical competency and tools.
  • Knowledge of utilities and project management.
  • All employees are responsible for complying with company documents, programs, and activities related to Health, Safety, Environment, Energy, and Quality Management Systems, as applicable to their roles.

Responsibilities

  • Design, communicate, implement, and complete complex engineering project plans in a manufacturing facility to improve productivity, capacity, or safety.
  • Implement site engineering projects using research, design, concept sketches, layouts, drawings, vendor interaction, specifications, and discussions with management and site personnel.
  • Ensure assigned management projects are completed within timeline and budget parameters.
  • Evaluate the feasibility of conceptual projects and prepare detailed analyses, including project completion time and cost and bills of materials.
  • Ensure assigned projects comply with applicable state, federal, and local codes, including environmental protection, FDA requirements, OSHA, and hazardous-waste requirements.
  • Direct and coordinate vendors on each project to eliminate potential conflicts and ensure vendors comply with safety rules and regulations.
  • Prepare and review project specifications, bid packages, and funding requests in accordance with corporate guidelines, including project descriptions, backgrounds, sketches, alternatives, financial data, justifications, quotations, estimates, and schedules.
  • Maintain awareness of pharmaceutical manufacturing needs and standards, and initiate programs or projects to advance the facility as a state-of-the-art pharmaceutical manufacturing site.
  • Communicate and report project status to departmental managers or the sponsoring department.
  • Prepare user requirement specifications, risk assessments, and safety assessments for projects when required.
  • Analyze complex production and processing problems and initiate project definitions to resolve them.
  • Collaborate with multiple functional teams.
  • Monitor and analyze energy consumption when applicable, identify energy-saving opportunities, and recommend ways to improve energy efficiency.
  • Maintain or improve the ISO 50001 energy management system when applicable.
  • Assist Manufacturing and Maintenance with problem-solving, process improvement, and cost reduction when applicable.
  • Execute projects in a Good Manufacturing Practices environment.
  • Review facility clean rooms.

Desired Qualifications

  • Pharmaceutical manufacturing industry experience.
  • Technical knowledge and understanding of statistical analysis tools and methods.
  • Computer literacy in word processing, spreadsheets, project management, and PowerPoint.

About the Company

cGMP Consulting

cGMP compliance consulting for pharma

cGMP Consulting helps pharmaceutical and biotech companies comply with current Good Manufacturing Practices (cGMP) and Title 21 CFR, offering engineering and quality assurance support. It works by performing gap analyses, then designing and implementing solutions for processes, documentation, validation, and technology adoption across international manufacturing sites. The company differentiates itself through hands-on, end-to-end support that combines technical engineering and QA expertise with practical implementation at multiple regulated sites. Its goal is to enable compliant, efficient global pharmaceutical manufacturing by helping clients adopt new technologies while meeting regulatory expectations.

Company size
51-200
Company stage
Not listed
Total funding
Not listed
Headquarters
Georgia, United States
Founded
2001

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