Traferox Technologies

Pharmaceutical

PharmaceuticalSolutionProcessEngineer

$75–90k Mississauga, Ontario, Canada FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for mid candidates.

The Brief

“Pharmaceutical Solution Process Engineer at Traferox Technologies. Skills: Pharmaceutical manufacturing, Process development, cGMP compliance. Design pharmaceutical manufacturing processes. Develop pharmaceutical manufacturing processes”

Industry & Context.

Pharmaceutical
Problems you'll solve

Problem-solving; Root cause analysis; Troubleshooting

What They're Looking For.

Must Have

2 years of experience in pharmaceutical manufacturing, Bachelor's or master’s degree in chemical or biotechnology engineering

Nice to Have

Knowledge of Microbiological evaluation methods, Experience with Lean manufacturing, Experience with Six Sigma, Experience with continuous improvement methodologies, Proficiency in computer applications such as MS Office, Proficiency in manufacturing execution systems (MES)

What You'll Do.

Design pharmaceutical manufacturing processes

Develop pharmaceutical manufacturing processes

Define operational parameters

Ensure compliance with regulatory guidelines

Ensure compliance with industry standards

Ensure compliance with Good Manufacturing Practices

Plan manufacturing activities

Schedule manufacturing activities

Meet production targets

Optimize resource utilization

Monitor manufacturing processes

Ensure product quality

Ensure product consistency

Ensure compliance with regulatory requirements

Evaluate manufacturing processes

Improve manufacturing processes

Enhance product quality

Conduct process troubleshooting

Conduct root cause analysis for deviations

Conduct root cause analysis for non-conformances

Conduct root cause analysis for quality issues

Identify process improvements

Implement process improvements

Implement procedural changes

Train manufacturing personnel on SOPs

Train manufacturing personnel on safety protocols

Train manufacturing personnel on best practices

Enhance team performance

Conduct inspections of manufacturing equipment

Conduct inspections of manufacturing facilities

Ensure proper operation of equipment

Ensure proper operation of facilities

Ensure cleanliness of equipment

Ensure cleanliness of facilities

Ensure maintenance of equipment

Ensure maintenance of facilities

Investigate deviations

Investigate non-conformances

Investigate quality incidents

Implement corrective actions

Implement preventive actions

Prevent recurrence of issues

Collaborate with Quality Assurance

Collaborate with Quality Control

Support investigations

Provide documentation

Provide technical expertise

Implement continuous improvement initiatives

Enhance manufacturing efficiency

Enhance product quality

Ensure compliance with environmental regulations

Ensure compliance with health regulations

Ensure compliance with safety regulations

Promote a culture of safety

Promote environmental stewardship

Maintain production records

Maintain batch documentation

Maintain inventory control records

How You'll Work.

Team & Collaboration

Collaborate across departments; Collaborate across levels

Communication Scope

Communication; Interpersonal skills

Full Job Description

Traferox creates, manufactures and commercializes products used to transplant solid organs (lungs, heart, liver, kidneys, pancreas). These products employ technologies invented by the transplant surgeons at the University Health Network (UHN). Traferox currently sells the TorEx Lung Perfusion System and the XPort Lung Transport Device. Traferox Technologies is committed to improving the outcomes of organ transplants and to save patients’ lives. [Traferox Technologies Inc.](https://traferox.com/) Union: Non-Union New or Replacement: New Department: Manufacturing Site: 2400 Skymark Ave. Unit 3, Mississauga, Ontario Reports to: Pharmaceutical Solution Manufacturing Supervisor Wage Range: $75,000 - $90,000 annually Hours: 37.5 Hours per Week Status: Permanent Full-time Number of vacancies: 1 Closing date: June 16, 2026 Duties and Responsibilities: * Design and develop pharmaceutical manufacturing processes, including equipment selection, process flow, and operational parameters. * Ensure compliance with regulatory guidelines, industry standards, and Good Manufacturing Practices (GMP) throughout process design and development. * Plan and schedule manufacturing activities to meet production targets while optimizing resource utilization and minimizing downtime. * Monitor manufacturing processes closely to ensure product quality, consistency, and compliance with regulatory requirements. * Continuously evaluate and improve existing manufacturing processes to enhance efficiency, yield, and product quality. * Conduct process troubleshooting and root cause analysis for deviations, non-conformances, and quality issues. * Identify and implement process improvements, such as equipment modifications, automation, or procedural changes, to optimize production and reduce costs. * Train manufacturing personnel on standard operating procedures (SOPs), safety protocols, and best practices to enhance team performance and skills development. * Conduct regular inspections of manufacturing e

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