Qualifications:
Graduation in Engineering or Technology based subjects(s).
3-5 years MES/related work experience
Relevant domain experience in manufacturing and/or quality operations.
Experience in all stages of solution and application lifecycle from value analysis, business
case development, and solution deployment through to value realization and system
...
retirement is a significant advantage.
Ability to work across multiple concurrent activities and successfully adapt to changing
priorities as required.
An understanding of system cGMP requirements and demonstrable knowledge of computer
system design and maintenance lifecycle in cGMP environments.
Experience working with Rockwell Pharma suite or Siemens OpCenter Execution Pharma.
Experience with Agile Software Delivery Software Tools: Rockwell Factory Talk Pharma Suite (FTPS MES), Siemens Opcenter
Execution Pharma, OPC Kepware.
Tools: HP Quality Center, HP ALM, JIRA, Service Now, CMRS, TrackWise (QTS), Microsoft
Office 365
Database Technologies: MS SQL, and Oracle using TOAD
Job Description/skills:
Should have Experience in Rockwell FTPS MES with Application configuration, building
Master Recipes and testing & validation.
Analyze and solve technical issues related to the MES and/ or solution development.
Creating the change controls for the Database updates using SQL queries to fix the
production issues and configuration changes in Qualified Environments.
Analysis of the requirements sent by the site SME’s and providing the solutions for
optimization.
Manage activities of user/ Functional Requirements Specification generation, software
configuration/testing and general oversight to the MES software documentation practices
Manage MES solution deployment, upgrade and solution/support process activities across
multiple sites and versions
Lead site recipe authoring teams to define standards and provide technical guidance and
support in the development of recipes (e.g. Template design strategies, EBR simplification,
etc.)
experience
30show more
Qualifications:
Graduation in Engineering or Technology based subjects(s).
3-5 years MES/related work experience
Relevant domain experience in manufacturing and/or quality operations.
Experience in all stages of solution and application lifecycle from value analysis, business
case development, and solution deployment through to value realization and system
retirement is a significant advantage.
Ability to work across multiple concurrent activities and successfully adapt to changing
priorities as required.
An understanding of system cGMP requirements and demonstrable knowledge of computer
system design and maintenance lifecycle in cGMP environments.
Experience working with Rockwell Pharma suite or Siemens OpCenter Execution Pharma.
Experience with Agile Software Delivery Software Tools: Rockwell Factory Talk Pharma Suite (FTPS MES), Siemens Opcenter
Execution Pharma, OPC Kepware.
Tools: HP Quality Center, HP ALM, JIRA, Service Now, CMRS, TrackWise (QTS), Microsoft
Office 365
Database Technologies: MS SQL, and Oracle using TOAD
Job Description/skills:
Should have Experience in Rockwell FTPS MES with Application configuration, building
...
Master Recipes and testing & validation.
Analyze and solve technical issues related to the MES and/ or solution development.
Creating the change controls for the Database updates using SQL queries to fix the
production issues and configuration changes in Qualified Environments.
Analysis of the requirements sent by the site SME’s and providing the solutions for
optimization.
Manage activities of user/ Functional Requirements Specification generation, software
configuration/testing and general oversight to the MES software documentation practices
Manage MES solution deployment, upgrade and solution/support process activities across
multiple sites and versions
Lead site recipe authoring teams to define standards and provide technical guidance and
support in the development of recipes (e.g. Template design strategies, EBR simplification,
etc.)
experience
30show more