Job Description

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 HP 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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