About the role
Experience -2- 15 yrs
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
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 HP 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.
Good communication skills
Able to work independently and have leadership skills.
Customer-oriented and committed to working systematically under tight schedules.
Develop and produce technical reports, process flow diagrams and documentation in support of design and developments.
Innovate, propose new ideas and define the technical approach to challenging problems.
