PAS-X MES Specialist – Life Sciences & ERP Integration

Accenture; Miami (FL); Remote; USD 39,000 - 136,000; Full time

Job summary

Accenture is seeking an ambitious Manufacturing Systems (MES) Specialist to drive MES design, development and deployment in highly automated Life Sciences environments. You will lead PAS-X MES projects, author Electronic Batch Records, and integrate MES with ERP and control systems to deliver compliant, value-added solutions.

You will collaborate with business leaders and users, ensuring MES configurations meet GxP standards and supporting documentation is thorough for audits and inspections.

Qualifications

• A minimum of 2 years of experience with Körber PAS-X MES solutions in a highly automated Life Sciences manufacturing environment.
• Knowledge of FDA and GMP guidelines.
• Bachelor's degree or equivalent (minimum 3 years work experience if Associate's Degree).

Responsibilities

• Lead in the design, development, documentation, and implementation of Körber PAS-X MES.
• Design/Author/Develop/Configure Electronic Batch Records (EBR).
• Implement MES solutions and integrate with ERP and control equipment.
• Documentation of MES configuration and validation of EBRs.
• Work closely with business management and users to define needs and design value-added solutions.
• Document and analyze information needs of the business per GxP standards.
• Respond to client proposals and manage client relationships.

Skills

Communication skills

Teamwork

Travel flexibility

Education

Bachelor's degree or equivalent

Tools

Körber PAS-X MES

ERP integration

EBR validation

Job description

Accenture is seeking an ambitious Manufacturing Systems (MES) Specialist to drive MES design, development and deployment in highly automated Life Sciences environments. You will lead PAS-X MES projects, author Electronic Batch Records, and integrate MES with ERP and control systems to deliver compliant, value-added solutions.

You will collaborate with business leaders and users, ensuring MES configurations meet GxP standards and supporting documentation is thorough for audits and inspections.