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Project Engineer, Manufacturing Engineer

Job in Mississauga, Ontario, Canada
Listing for: BioSpace
Full Time position
Listed on 2026-02-23
Job specializations:
  • Engineering
    Manufacturing Engineer, Process Engineer, Quality Engineering, Validation Engineer
Salary/Wage Range or Industry Benchmark: 75000 CAD Yearly CAD 75000.00 YEAR
Job Description & How to Apply Below
Join to apply for the  Project Engineer  role at  Bio Space .

A career at Resilience is more than just a job – it’s an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high‑tech, end‑to‑end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.

For more information, please visit

Job Summary
The Project Engineer provides advanced engineering support in a GMP biopharmaceutical environment. This role requires strong technical capability, independent leadership, and cross‑functional collaboration in the execution of complex projects, equipment implementation, and production support activities.

Major Responsibilities

Provide leadership in the execution of complex technical projects, coordinating efforts across internal and external stakeholders to ensure alignment, efficiency, and regulatory compliance.

Act as a key interface with clients and stakeholders to align project deliverables with expectations and objectives.

Lead coordination efforts with design, construction, and internal teams to execute capital and client projects.

Develop and define specifications for systems and equipment within the project scope, including drafting comprehensive user requirement specifications (URS).

Hands‑on experience in equipment design for biopharmaceutical manufacturing, including aseptic Fill/Finish operations, bioreactors, chromatography systems, and filtration.

Experience with utilities design and operation, including purified water systems (PW), water for injection (WFI), compressed air, and clean steam.

Experience with cleanroom design/grades/classifications, GMP flows, and HVAC design principles.

Evaluate and review bids, design documents, quotations, and functional specifications to ensure alignment with project requirements, technical specifications, and budget constraints.

Assess compliance with regulatory requirements from agencies such as the FDA, EMA, and HC for process systems and components, ensuring adherence to current Good Manufacturing Practices (cGMP).

Ensure systems meet Environmental Health and Safety (EHS) standards and regulatory requirements, promoting a safe and compliant work environment.

Coordinate, review, and execute Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) to validate system functionality before deployment.

Identify, investigate, and resolve deviations from user and system specifications, ensuring corrective actions are effectively implemented.

Draft and execute commissioning and qualification protocols, including Installation Qualification (IQ) and Operational Qualification (OQ).

Support manufacturing start‑up, including engineering trials, troubleshooting, and process validation activities.

Production / Manufacturing Support

Provide technical mentorship and guidance to junior team members and peers, fostering knowledge sharing and development within the team.

Collaborate with cross‑functional teams including quality, validation, maintenance, and operations to support site and project objectives.

Diagnose and troubleshoot equipment and process‑related issues to minimize downtime and optimize performance.

Identify and implement process improvements aimed at enhancing production rates, increasing yields, and improving uptime.

Prepare and present detailed technical reports on manufacturing systems, processes, and operational efficiencies such as risk assessments and protocols.

Support scale‑up activities by assisting in process optimization and validation for large‑scale production.

Develop and review SOPs to standardize best practices and maintain compliance with regulatory guidelines.

Maintain and update engineering drawings under strict change‑control procedures to ensure accurate documentation of modifications.

Minimum Qualifications

Experience in GMP or regulated production environment.

Experience in a manufacturing or operations‑based field/industry involving a fast‑paced, customer‑oriented environment.

Ability to direct self and others in a project environment.

Experience in demonstrating…
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