MES Consultant (Pharmaceutical Manufacturing)

Location: Canada or the United States; the role description specifies the United States

Company

Independent technology consulting firm delivering solutions across information systems, digital, telecom, life sciences, and engineering for clients worldwide.

What you will do

• Design, configure, maintain, and optimize MES applications supporting pharmaceutical manufacturing operations.
• Translate production, quality, and IT requirements into effective MES solutions.
• Integrate MES with ERP, LIMS, SCADA, and related manufacturing systems.
• Troubleshoot MES issues and minimize disruption to manufacturing processes.
• Provide user support, training, and system documentation.
• Contribute to system upgrades, migrations, validation, and continuous improvement projects.

Requirements

• Strong experience with MES platforms, preferably in pharmaceutical or life sciences environments.
• Experience or familiarity with PAS-X is preferred.
• Understanding of GMP and other manufacturing regulatory requirements, including FDA standards.
• Experience integrating ERP, SCADA, LIMS, or related systems.
• Strong problem-solving and communication skills for collaboration with technical and business stakeholders.
• Bachelor’s degree in Engineering, Computer Science, or a related field.

Culture & Benefits

• International community representing more than 110 nationalities.
• Internal Academy with more than 250 training modules.
• Career development environment with many leaders progressing from entry-level roles.
• Regular internal events, including afterworks and team-building activities.

Hiring process

• Brief virtual or phone call.
• Approximately three interviews, depending on seniority.
• Potential case study, technical assessment, role play, or problem-solving exercise.