Pharmaceutical Solution Process Engineer

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:  $75000 - $90000 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 equipment and facilities to ensure proper operation cleanliness and maintenance.
• Investigate deviations non-conformances and quality incidents implementing corrective and preventive actions as necessary to address root causes and prevent recurrence.
• Collaborate with Quality Assurance and Quality Control departments to support investigations audits and inspections providing relevant documentation and technical expertise.
• Implement continuous improvement initiatives to enhance manufacturing processes efficiency and product quality utilizing tools such as Lean manufacturing and Six Sigma methodologies.
• Ensure compliance with environmental health and safety regulations in all manufacturing activities promoting a culture of safety and environmental stewardship.
• Maintain accurate production records batch documentation and inventory control records in compliance with regulatory requirements and company policies.

Qualifications :

Education:

• Bachelors or masters degree in chemical or biotechnology engineering or a related field.

Experience:

• Minimum of 2 years of experience in pharmaceutical manufacturing. Knowledge of Microbiological evaluation methods is very beneficial.

Skills and Knowledge:

• Thorough understanding of cGMP regulations FDA guidelines and industry best practices related to pharmaceutical manufacturing.
• Strong leadership skills with the ability to motivate and develop a diverse workforce.
• Excellent communication and interpersonal skills with the ability to collaborate effectively across departments and levels of the organization.
• Demonstrated problem-solving abilities and a proactive approach to addressing manufacturing challenges and process improvements.
• Experience with Lean manufacturing Six Sigma or other continuous improvement methodologies is desirable.
• Proficiency in computer applications such as MS Office and manufacturing execution systems (MES) is preferred.
• Flexibility to work in a fast-paced environment and adapt to changing priorities and business needs.
• Strong attention to detail organizational skills and a commitment to upholding the highest standards of product quality and regulatory compliance.

Additional Information :

We thank all applicants for their interest in this position with Traferox Technologies Inc. Please note that only candidates selected for an interview will be contacted.  

Remote Work :

No

Employment Type :

Full-time