Sr Process Engineer

Catalyx

$90K — $120K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in relevant engineering discipline or equivalent experience.
  • Member of the Ordre des ingénieurs du Québec (OIQ).
  • 10+ years of experience in the pharmaceutical industry, particularly in sterile injectable manufacturing.
  • 5+ years of project management experience.
  • Bilingual in French and English for supplier interactions.

Responsibilities

  • Oversee the startup and optimization of new equipment.
  • Provide technical support to manufacturing operations during execution.
  • Troubleshoot technical issues directly on production lines.
  • Improve key performance indicators (KPIs).
  • Design and implement technical modifications to optimize equipment performance.
  • Plan projects in coordination with various departments to minimize production impact.
  • Use Lean and Six Sigma tools to analyze equipment and processes.

Benefits

  • Opportunity to lead and manage diverse projects.
  • Engagement in continuous improvement initiatives.
  • Work within a collaborative team environment.
  • Access to professional development and training.
  • A chance to influence production efficiency and quality.
Full Job Description
Job Description
Catalyx is seeking a Senior Process Engineer to provide technical problem-solving support for production equipment issues, offer technical support to manufacturing teams during operations, and works to reduce recurring equipment-related deviations. They also collaborate in responding to audit observations, customer requests, and other technical inquiries as needed.

Responsibilities

Technical & Operational Support
• Oversee the startup and optimization of new equipment.
• Provide technical support to manufacturing operations during execution.
• Participate in solving complex technical problems (troubleshooting).
• Design equipment modifications while meeting aseptic and operational requirements.
• Troubleshoot technical issues directly on production lines.
• Analyze machine downtime and recommend corrective actions.
• Participate in the commissioning of new equipment.

Performance & Process Optimization
• Improve key performance indicators (KPIs).
• Optimize production and maintenance processes.
• Develop and implement fast and effective troubleshooting solutions.
• Design and implement technical modifications to optimize equipment performance.
• Prepare control changes, procedures, and documentation required to implement improvements and solutions.

Project Management & Documentation
• Prepare intervention reports and technical procedures.
• Ensure compliance with safety and environmental regulations.
• Define project requirements and prepare feasibility studies.
• Communicate with equipment suppliers.
• Plan projects in coordination with Production, Engineering, Maintenance, Quality Assurance, and contractors to minimize production impact.
• Monitor project execution, including inspections, schedules, meetings, and communications.
• Ensure proper project closeout, including budgets, documentation, and change controls (CCs).
• Continuous Improvement & Leadership
• Use Lean and Six Sigma tools to analyze equipment utilization, labor efficiency, and machine performance to reduce waste and improve productivity.
• Provide leadership as a project manager.
• Participate in Continuous Improvement and Aseptic committees.
• Perform other administrative duties as assigned by the manager.

Requirements

Qualifications
• Bachelor's degree in Mechanical Engineering, Electrical Engineering, Industrial Engineering, Chemical Engineering, Automation Engineering, or equivalent experience.
• Member of the Ordre des ingénieurs du Québec (OIQ).
• Minimum 10 years of experience in the pharmaceutical industry, specifically in sterile injectable manufacturing.
• Minimum 5 years of project management experience.
• Strong knowledge of aseptic manufacturing processes.
• Experience in equipment troubleshooting and modification (an asset).
• Strong analytical thinking, autonomy, customer service orientation, and interpersonal skills.
• Excellent analytical and technical problem-solving abilities.
• Strong knowledge of mechanical, electrical, and automated systems.
• Excellent communication and teamwork skills.
• Ability to manage multiple projects simultaneously.
• Ability to perform well under pressure and adapt to changing priorities.
• Bilingual in French and English, due to interactions with out-of-province suppliers.
• Strong communication skills and a sense of urgency in prioritizing work.
• Team-oriented with strong collaboration skills.
• Proficient in Microsoft Office tools, including AutoCAD, MS Project, and Visio.
• Knowledge of CAD and CMMS (Computerized Maintenance Management System) software.

Experience

Required
• Minimum 10 years of experience in the pharmaceutical industry, specifically in sterile injectable manufacturing.

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