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GMP Engineering Inc.

Junior Process Engineer (2027 Grad)

Oakville, ON, Canada

$70,000 to $75,000 USD / year · Full-time

Within 25 km of Milton · About 22.2 km from the city centre

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Job details

Pay: $70,000 to $75,000 USD / year
Job type: Full-time
Apply by: Mar 30, 2027
Posted: Oct 1, 2026

Original job description

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.

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More about this job

Responsibilities

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.

Skills

Process Design
Process Engineering
Design Basis Development
Process Alternatives Evaluation
Process Flow Diagrams
Piping And Instrumentation Diagrams
Process Integration
Equipment Sizing And Specification
Commissioning And Qualification
Cross-Functional Team Coordination
Project Prioritization
Written And Verbal Communication
Teamwork

Visa sponsorship

Not detected in the job text

Keywords

GMP Compliance
Pharmaceutical Manufacturing
Bio-Pharmaceutical
Process Equipment
Sterile Processing
High-Purity Processing
Potent Containment
Design Basis
Process Alternatives Evaluation
Process Flow Diagrams
Piping And Instrumentation Diagrams
Process Integration
Unit Operations
Equipment Sizing
Equipment Specification
Plot Plans
Layout Drawings
Commissioning
Qualification
Validation
Factory Acceptance Tests
Cross-Functional Engineering
Food Industry
Personal Care Industry

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