Mes Analyst

2 weeks ago

Jurong East, Singapore Quess Corp Limited Full time

Job Information:

Industry

Manufacturing
***Salary

9000
***Work Experience

6-8 Years
***City

Jurong East Street 13
***State/Province

JURONG East
***Country

Singapore
***Zip/Postal Code

600101
***
Roles & Responsibilities:
  • Define User requirement specifications (Voice of customer)
  • Design and create Master Batch Record batch files (MBR) with respect for quality, costs and deadlines
  • MBR / BOM/ Recipe creation in Werum PAS-X.
  • Participate in the qualification and risk assessment processes
  • Propose and technically validate the choice of solutions proposed by the IT teams and Automation in collaboration with the Quality team
  • Participate to the deployment of MES across the manufacturing units, runs performance qualification and validation batches (commissioning of the line) with the manufacturing units
  • Responsible for the manufacturing documentation update following the implementation of electronic batch files
  • Provide training for MES users in partnership with the training team
  • Support and followup of deviations and Change Control in compliance with deadlines and applicable regulations
  • Realtime shop floor troubleshooting with the implementation of appropriate immediate corrective actions
  • Ensure the transfer of information to production teams following issues or modifications having a technical, quality or HSE impact
  • Responsible for MES technical knowledge transfer to the shop floor
  • Ensure the preparation of audits and inspections for related topics
  • Collaborate with process experts in the context of deviations related to MES and

Requirements:

  • Minimum of 58 years experience in a similar role, ideally in the Pharmaceutical industry.
  • Recipe Authoring, MBR Development, and Equipment Management in Werum PAS-X
  • Subject matter expert for Werum PAS-X production IT systems
  • Expertise in MBR design, OSI-PI, interface with SAP and Trackwise
  • Strong understanding of Pharmaceutical or Biopharmaceutical process
  • Understanding of L2 interfaces and integration with MES
  • Familiarity with SDLC and quality management processes in the pharma
  • Ability to work well in a team environment.
  • Able to manage multipleparty coordination for MES information

Benefits:

  • AL : 14 Days

ML :
14 days