MES Consultant

AMARIS GROUP SA; United States; On-site; USD 80,000 - 100,000; Full time

Job summary

AMARIS GROUP SA is seeking a MES (Manufacturing Execution System) Consultant/Engineer to join its team in the United States. This role is crucial for supporting digital manufacturing initiatives within the pharmaceutical sector, ensuring effective design and implementation of MES solutions.

The successful candidate will collaborate with cross-functional teams to enhance system reliability, improve manufacturing processes, and ensure compliance with regulatory requirements. Strong experience with MES platforms, especially in pharma, and effective communication skills are essential.

Qualifications

• Strong experience with MES platforms, preferably 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.
• Experience with system integration (ERP, SCADA, LIMS, or related).

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 to minimize disruption to manufacturing processes.
• Provide user support, training, and documentation for system utilization.

Skills

MES platforms

GMP and regulatory requirements

System integration (ERP, SCADA, LIMS)

Problem-solving skills

Excellent communication skills

Education

Bachelor’s degree in Engineering, Computer Science, or related field

Tools

PAS-X

Job description

We are seeking a MES (Manufacturing Execution System) Consultant / Engineer to join our team within the pharmaceutical industry in United States. This role is key in supporting digital manufacturing initiatives by ensuring the effective design, implementation, and optimization of MES solutions. The successful candidate will collaborate with cross‑functional teams to enhance system reliability, improve manufacturing processes, and ensure compliance with regulatory requirements. Experience with PAS-X is a strong plus.

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, preferably 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.

Amaris Consulting promotes equal opportunities. We are committed to bringing together people from diverse backgrounds and creating an inclusive work environment. In this regard, we welcome applications from all qualified individuals, regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.