MES Consultant

Amaris Consulting; United States; On-site; USD 85,000 - 110,000; Full time

Job summary

Amaris Consulting is seeking a MES (Manufacturing Execution System) Consultant in the United States. This role involves designing, implementing, and optimizing MES solutions in the pharmaceutical industry, ensuring compliance with regulatory standards. The successful candidate will work collaboratively with teams to enhance system reliability and improve processes.

Qualifications include strong experience with MES platforms, understanding of GMP requirements, and a Bachelor’s degree in a related field. The position promotes equal opportunities and values diverse backgrounds.

Qualifications

• Strong experience with MES platforms, preferably in the pharmaceutical or life sciences industry.
• Familiarity with PAS-X is preferred but not mandatory.
• Ability to work under strict compliance standards.

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.

Skills

Experience with MES platforms

Understanding of GMP and regulatory requirements

Problem-solving skills

Excellent communication skills

Education

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

Tools

PAS-X

ERP

LIMS

SCADA

Job description

Job Description: MES (Manufacturing Execution System) Consultant / Engineer in the pharmaceutical industry in the United States. This role supports 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.

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.

Qualifications

• 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.

EEO Statement: Amaris Consulting promotes equal opportunities and is committed to creating an inclusive work environment. Applications from all qualified individuals are welcome regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.