Tevapharm India Pvt. Ltd.
Education and Professional experience Requirements:
Relevant academic background in computer since and IT systems
MES certification or SAP MES cerfication is added advantage
At least 3-5+ years’ experience with MES (preferable Werum PAS-X)
3-5+ years’ experience related to Testing and Validation of Manufacturing IT Systems
At least 3 years working experience in MES Testing/QA departments
Experience in an FDA regulated or regulated industry beneficial, preferable in in Pharmaceutical
manufacturing
In-depth knowledge of industry standards (such as Good Manufacturing Practices, GAMP, ISA 95,
ISA 88, 21CFR part 11 is preferred)
Deep knowledge on Master data wrt SAP Manufacturing
Should have good knowledge on Material master interfaces channels
BOM, Resource, Recipe and Production version interfaces channels
Batch master interfaces channels
Inbound interfaces like
Process order creation and release
Operation start and End time
Goods Issues against process order
Goods receipt against process order
Outbound interfaces like
MES to Process order update
MES to Batch data update
MES to process order Batch allocation
MES to Stock transfer order
Deep knowledge on Manual testing
Experience with Micro Focus ALM & UFT tools is an advantage
Experience with worldwide projects in global companies
ERP/SAP Implementation experience
Pharmaceutical/regulatory experience is an advantage
Experience working from offshore
Job Details
Employment Type Permanent