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Job Description
Key Responsibilities:
Perform end-to-end Manual Testing for MES (Manufacturing Execution System).
Create and execute functional, regression, and validation test cases.
Log, track, and resolve defects using test management tools.
Coordinate testing activities with cross-functional teams.
Prepare testing documentation and ensure compliance with regulatory standards.
Support integration testing between MES, SAP, LIMS, and other manufacturing systems.
Required Skills:
3–5+ years of MES Testing experience (Preferably Werum PAS-X).
Strong experience in Manual Testing and QA of Manufacturing IT Systems.
Good understanding of SAP Manufacturing master data and interfaces (Material Master, BOM, Recipe, Resource, Production Version, Batch Master).
Knowledge of inbound/outbound interfaces, Process Orders, Goods Issue/Receipt, and Batch updates.
Experience with Micro Focus ALM/UFT is an added advantage.
Understanding of GMP, GAMP, ISA-95, ISA-88, and 21 CFR Part 11 is preferred.
ERP/SAP implementation and Pharmaceutical domain experience are highly preferred.
MES/SAP MES Certification (Good to have).
Experience working on global/offshore projects.
Good communication and stakeholder management skills
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





