Job Description

MES Apriso Developer :-


Core Technical & Domain Expertise

  • 2 to 10 years of hands-on experience in e BMR / MES implementation within regulated pharmaceutical or life sciences environments
  • Proven expertise in end-to-end e BMR lifecycle including design, configuration, execution, review by exception (RBE), and batch release
  • Deep understanding of pharmaceutical manufacturing processes (Dispensing, Weighing, Granulation, Compression, Coating, Packing, Sterile / Non-sterile operations)
  • Strong experience working with MES/e BMR or equivalent enterprise MES platforms (We rum PAS-X, Siemens OpsCenter, Rockwell FactoryTalk, etc.)



Regulatory & Validation Expertise

  • Expert-level knowledge of GMP, GAMP 5, 21 CFR Part 11, EU Annex 11, W...

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