About the role
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.
Not the right fit? Search for Process Engineer jobs in Oakville, Ontario, Canada
About GMP Engineering Inc.
GMP Engineering is a unique process technology-rooted engineering company adhering to the standards of current Good Manufacturing Practices (cGMP). We use our expertise to provide customer driven solutions specializing in hygienic, sterile and high containment process equipment design and validation. We provide high-quality consulting and engineering services with broad international project experience across North America, Europe, and Japan.
Our clients are producers of pharmaceutical, biotechnological, biological, and personal care products that employ current Good Manufacturing Practices (cGMP) and meet the highest standards of quality.
GMP Engineering’s core capabilities are in the execution of technology-driven projects in pilot-plant and production-scale process facilities. We provide process engineering, facility design, and regulatory compliance support for operations in the life sciences sector and other clean process industries.
Our company has comprehensive project capabilities to manage and execute feasibility studies, conceptual design, preliminary engineering, detailed design, construction administration, commissioning and qualification.
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About the role
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.
Not the right fit? Search for Process Engineer jobs in Oakville, Ontario, Canada
About GMP Engineering Inc.
GMP Engineering is a unique process technology-rooted engineering company adhering to the standards of current Good Manufacturing Practices (cGMP). We use our expertise to provide customer driven solutions specializing in hygienic, sterile and high containment process equipment design and validation. We provide high-quality consulting and engineering services with broad international project experience across North America, Europe, and Japan.
Our clients are producers of pharmaceutical, biotechnological, biological, and personal care products that employ current Good Manufacturing Practices (cGMP) and meet the highest standards of quality.
GMP Engineering’s core capabilities are in the execution of technology-driven projects in pilot-plant and production-scale process facilities. We provide process engineering, facility design, and regulatory compliance support for operations in the life sciences sector and other clean process industries.
Our company has comprehensive project capabilities to manage and execute feasibility studies, conceptual design, preliminary engineering, detailed design, construction administration, commissioning and qualification.