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MES Consultant
Miami Lakes, United States
Roles & Responsibilities:
- 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.
- 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 customers 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 the customer side.
- Develop and produce technical reports, process flow diagrams and documentation in support of design and developments.
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