MES Consultant / Engineer

Amaris Consulting; Toronto; On-site; CAD 85,000 - 110,000; Full time

Benefits offered by this job

International community

Training system with over 250 modules

Dynamic work environment with internal events

Job summary

A global consulting firm in Toronto is seeking a MES Consultant/Engineer to support digital manufacturing initiatives in the pharmaceutical industry. The role involves designing and maintaining MES applications, ensuring compliance with industry standards, and collaborating with various teams. Ideal candidates should have strong experience with MES platforms and a relevant degree. A supportive and dynamic work environment is offered.

Qualifications

• Strong experience with MES platforms in the pharmaceutical or life sciences industry.
• Familiarity with PAS‑X is preferred but not mandatory.
• Understanding of GMP and regulatory requirements in manufacturing environments.

Responsibilities

• Design, configure, and maintain MES applications to support manufacturing operations.
• Collaborate with production, quality, and IT teams to translate business needs into MES solutions.
• Support the integration of MES with ERP, SCADA, and other manufacturing systems.

Skills

MES platforms experience

Problem-solving skills

Communication skills

Education

Bachelor’s degree in Engineering or Computer Science

Job description

Job Description

We are seeking a MES (Manufacturing Execution System) Consultant / Engineer to join our team within the pharmaceutical industry in Toronto. This role is key in supporting digital manufacturing initiatives by ensuring the effective design, implementation, and optimization of MES solutions.

Key Responsibilities

• Design, configure, and maintain MES applications to support manufacturing operations.
• Collaborate with production, quality, and IT teams to translate business needs into MES solutions.
• Support the integration of MES with ERP, LIMS, SCADA, and other manufacturing systems.
• Troubleshoot MES-related issues, ensuring minimal disruption to manufacturing processes.
• Provide user support, training, and documentation to enable effective system utilization.
• Ensure compliance with GMP, FDA, and other regulatory standards in system configuration and validation.
• Contribute to system upgrades, migrations, and continuous improvement initiatives.
• Participate in project delivery within an agile or structured project framework.

Requirements

• Strong experience with MES platforms in the pharmaceutical or life sciences industry.
• Familiarity with PAS‑X (preferred but not mandatory).
• Understanding of GMP and regulatory requirements in manufacturing environments.
• Experience with system integration (ERP, SCADA, LIMS, or related).
• Strong problem‑solving skills and ability to work under strict compliance standards.
• Excellent communication skills for collaboration with technical and business stakeholders.
• Bachelor’s degree in Engineering, Computer Science, or a related field.

Why choose us

• An international community with 110+ nationalities.
• Trust‑based environment: 70% of leaders started at entry level.
• Strong training system with internal Academy and over 250 modules.
• Dynamic work environment with regular internal events.

Amaris Consulting promotes equal opportunities. We welcome applications from all qualified individuals, regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.