Location: Remote
Employment Type: Full-time / Contract (W2 only)
Job Description:
We are seeking an MES Engineer with strong experience in Rockwell FactoryTalk PharmaSuite (FTPS) to lead the design, development, and implementation of MES solutions in a Life Sciences / FDA-regulated environment . This role will involve authoring and validating Electronic Batch Records (EBRs) , integrating MES with ERP and automation systems, and ensuring compliance with FDA, GMP, and GxP standards .
Responsibilities:
Lead design, configuration, and validation of Rockwell PharmaSuite MES solutions
Design/author/develop Electronic Batch Records (EBR)
Integrate MES with ERP and automation/control systems
Document MES configurations and validation processes
Work with stakeholders to define requirements and deliver compliant solutions
Support SDLC and Life Sciences validation processes
Basic Qualifications:
5+ years of professional experience
Minimum 1 year of hands-on experience with Rockwell PharmaSuite MES in a Life Sciences environment
Strong knowledge of FDA, GMP, and GxP guidelines
Experience with validation and compliance processes in Life Sciences manufacturing
Understanding of SDLC and support methodologies
Flexibility for travel (0 100% based on business/client needs)
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