POSITION:You will be part of a cross-functional engineering team in the role of Jr. Process Designer (/Engineer if you hold a P.Eng.). You will develop and deliver conceptual, preliminary, and detailed design packages through to CQV for GMP-compliant integrated process equipment and unit operations used in the manufacturing of pharmaceutical drug substances and products.SUMMARY:Working under the guidance of a senior engineer you will be responsible for:Design Basis DevelopmentProcess Alternatives EvaluationsUser Requirement Specifications (URS)Process Flow Diagrams (PFDs)Process Piping and Instrumentation Diagrams (P&IDs)Process Integration of Unit OperationsEquipment Plot Plans and Layout DrawingsEquipment Sizing and SpecificationCommissioning & Qualification Protocol Development and ExecutionSKILLS:Strong interpersonal skills and the ability to work in a team setting.Ability to manage and coordinate cross-functional project teams.Ability to prioritize multiple tasks.Self-directed, resourceful, and able to work independently with minimal oversight.Excellent written and verbal communication skills.Ability to work effectively in a fast-paced multi-tasking environment.LOCATION:The primary work location will be in our main Oakville, ON office. However, a significant aspect of the role will involve intermittent international travel, including extended periods (up to 50%) spent at equipment vendors for Factory Acceptance Tests (FATs) and at the client's site for Commissioning, Qualification, and Validation (CQV) activities.

📌 Junior Process Engineer (Oakville)
🏢 GMP Engineering
📍 Oakville