Canada, Charlottetown
Fulltime: 40 hrs a week
Experience: 4-6 Years
Education Level: Academic Bachelor
Life Sciences
Closing: June 23, 2025

Introduction

Industrial Engineer Charlottetown, PEI

What are you going to do 

Responsibilities

  • Assist in the planning, execution, and monitoring of capital and infrastructure projects, ensuring alignment with project goals, timelines, and budgets.
  • Lead process and equipment validation ensuring regulatory compliance and consistent high-quality products.
  • Monitor production data and Key Performance Indicators (KPIs) to highlight trends and opportunities for improvements.
  • Ensure that all manufacturing processes and equipment meet the required standards and specifications through rigorous testing and validation.
  • Follow IQ, OQ, PQ methodologies when applicable.
  • Develop and manage qualification documentation for new equipment, processes, and systems, ensuring accuracy and completeness.
  • Track the status of qualification activities and provide regular updates to stakeholders on progress and issues.
  • Conduct assessments of packaging materials and processes to ensure they meet quality, safety, and compliance standards.
  • Provide recommendations for packaging improvements and partner with suppliers and internal teams to implement changes.
  • Identify and implement strategies and methodologies (Lean, Six Sigma) for continuous improvements, efficiency gains, and waste reduction including tracing performance of implemented changes.

Essential skills and knowledge 

Requirements

  • Bachelor's degree in mechanical or electrical engineering
  • 5+ years engineering experience working in a manufacturing company; pharmaceutical experience preferred.
  • Certification in Lean Six Sigma or other process improvement methodologies would be considered an asset.
  • Strong critical thinking and problem-solving skills to identify and implement improvements in production processes
  • Ability to manage multiple projects and prioritize tasks effectively
  • Keen attention to detail with strong documentation and organizational skills
  • Excellent communication and presentation skills
  • Competent with MS Office and AutoCAD
  • Familiarity with GMP (Good Manufacturing Practices) and other relevant regulatory standards in the pharmaceutical industry.
  • Proven experience in managing projects from conception through completion, including budgeting and timeline management.
  • Experience with manufacturing software and systems, such as ERP (Enterprise Resource Planning) systems

What we offer 

What We Offer

Why apply through Brunel? Finding the next step in your career can be a fulltime job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with on-boarding. We'll get you going while you get on with the job.

About Us

Brunel has a reputation for working with some of the best in the business. That's what we continually strive for. Over 45 years, we've created a global network of interesting clients and talented individuals working together through a vast array of services.

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