Werum PAS-X MES MBR Designer

Posted by Zenith Technologies on 10/02/2020 (14:59)

Dublin, Dublin City
10/02/2020 (14:59)
Zenith Technologies

Werum PAS-X MES MBR Designer  - Dublin – JO 1613

Zenith Technologies  are currently looking to hire Werum PAS-X MES MBR Designer  to join our client’s offices in Dublin.


  • Create business process flow diagram for pharmaceutical product recipes based on the paper batch record or source documents

  • Gather MES Site specific requirement analysis to develop URS and FRS

  • Logically breakdown the recipes/Mfg. process to configure the recipe in to Werum PAS-X

  • Develop/create MBR design elements (building blocks) and workflows in Werum PAS-X for repetitive use in MBR creation to expedite the process

  • Gather master data and configure in Werum PAS-X Development/Quality/Production Environment.

  • Integrating Werum PAS- X with SAP and other automation systems using standard interface component of MBR design.

  • Lead the recipe design session with business process SMEs

  • Design MBR/recipe, equipment workflow/ status diagram based on the Business process flow

  • Create solution design and configuration document

  • Assist Validation engineer in authoring and execution of OQ/SITs including Interface testing

  • Support Unit testing in D environment and business verification testing in Q environment

  • Prepare key user training documents and impart key user training
  • Provide assistance in business SOP creation

  • Support FAT/UAT execution
  • Perform go-live/ cut-over activities
  • Provide hypercare/early life adoption support

Qualifications/ Requirements:

  • Bachelor’s Degree in engineering / science
  • Total 5+ years of hands-on experience on MES Product, Min 3+ years in MBR designing role
  • Werum PAS-X product hands-on experience for Full application configurations including interface with SAP and automation systems
  • In-depth of knowledge of Pharmaceutical business process (Chemicals (W&D, Solid bulk Mfg., packaging and other unit operations), Bio Pharma processes)
  • Creation of business process flow diagram
  • Master Batch Record creation in Werum PAS-X
  • Knowledge on Industry Standards S88 and ISA S95
  • Pharmaceutical validation concept
  • cGMP and GDP standards and GAMP Standards
  • Good verbal, written communication
  • Team skill
Contract Length:
Job Reference:
Job ID:
Less than 10

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