Sr.MES Consultant

Roles & Responsibilities: Must have basic knowledge or understanding of Pharmaceutical/Medical Device compliances like 21 CFR Part 11 Compliance, GAMP, GDP etc. Previous work experience in MES implementation using any platform. Must have hands-on experience on testing tools like Client ALM, Polarion etc. Excellent English skills, both spoken and written. Collaborate as a project team member and directly with customer on requirement gathering, master data modelling and enrichment, giving Demos on core and new concepts to SMEs and End users. Working collaboratively and helping cross-cultural and cross-regional team members - both internal and on customer side. Develop and produce technical reports, process flow diagrams and documentation in support of design and developments Education & Experience: 10+ years of MES experience in Manufacturing and Medical Device Domain (MDD). 5+ years of working experience in managing Critical Manufacturing MES implementations and Rollouts, master data modelling and enrichment. Certified Critical Manufacturing Professional / Associate: Modeler

Created: 2026-03-04