Industrial Engineer

Brunel International; Charlottetown; On-site; CAD 70,000 - 110,000; Full time

Job summary

An established industry player is seeking a skilled engineer to lead and manage capital and infrastructure projects. This role involves ensuring compliance with regulatory standards while enhancing production processes through critical thinking and problem-solving. You will be responsible for developing qualification documentation, tracking project progress, and implementing Lean Six Sigma methodologies for continuous improvement. Join a dynamic team where your expertise will drive efficiency and quality in manufacturing, particularly within the pharmaceutical sector. If you are passionate about engineering and have a keen eye for detail, this opportunity is perfect for you.

Qualifications

• 5+ years of engineering experience in manufacturing, preferably in pharmaceuticals.
• Certification in Lean Six Sigma or similar methodologies is a plus.

Responsibilities

• Assist in planning and monitoring capital projects to meet goals and budgets.
• Lead validation processes ensuring compliance and product quality.
• Identify strategies for continuous improvements and efficiency gains.

Skills

Critical Thinking

Problem Solving

Project Management

Lean Six Sigma

Communication Skills

Documentation Skills

Education

Bachelor's Degree in Mechanical Engineering

Bachelor's Degree in Electrical Engineering

Tools

MS Office

AutoCAD

ERP Systems

Job description

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