Junior Process Engineer (2027 Grad)

Job summary

Develop conceptual, preliminary, and detailed design packages for GMP-compliant process equipment and unit operations used in pharmaceutical manufacturing. Support design development, equipment integration and specification, and the development and execution of commissioning and qualification activities.

Job details

We are a specialized engineering company with international exposure and subject matter expertise in the design, fabrication and qualification of sterile, high purity and potent containment process equipment and plants. We are growing our company size and capabilities through recruitment of talented professionals. We offer a true creative engineering design work environment with a wide range of interesting projects in the bio-pharmaceutical, personal care and food industry. 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 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 environment. 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. EDUCATION: Bachelor’s degree in engineering 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. **APPLICATION INSTRUCTIONS: Please attach a single merged PDF and include both your resume and your unofficial transcript.

What you’ll do

Develop conceptual, preliminary, and detailed design packages for GMP-compliant process equipment and unit operations used in pharmaceutical manufacturing. Support design development, equipment integration and specification, and the development and execution of commissioning and qualification activities.

Requirements

A bachelor's degree in engineering is required; the role is intended for a junior-level or 2027 graduate candidate. Candidates should have strong communication, teamwork, task prioritization, and cross-functional coordination skills, and be able to work independently in a fast-paced environment.

Listed skills

• Teamwork · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Process Design
• Process Engineering
• Design Basis Development
• Process Alternatives Evaluation
• User Requirement Specifications
• Process Flow Diagrams
• Piping And Instrumentation Diagrams
• Process Integration
• Equipment Sizing And Specification
• Plot Plans And Layout Drawings
• Commissioning And Qualification
• Cross-Functional Team Coordination
• Project Prioritization
• Written And Verbal Communication
• Teamwork

Job areas

• Engineering
• Manufacturing
• Science & Research