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 Development
- Process Alternatives Evaluations
- User Requirement Specifications (URS)
- Process Flow Diagrams (PFDs)
- Process Piping and Instrumentation Diagrams (P&IDs;)
- Process Integration of Unit Operations
- Equipment Plot Plans and Layout Drawings
- Equipment Sizing and Specification
- Commissioning & Qualification Protocol Development and Execution
SKILLS:
- 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.