Hi
MES Consulting
Location: Kenosha, WI
Duration: 6 months
Role Descriptions:
Understanding of pharmaceutical manufacturing processes (Solid oral dose and packaging preferred) Possesses expertise in Good Documentation and Good Testing Practices
Ability to process map site requirements using Microsoft Visio or alike software
Ability to work with site SMEs to turn paper batch records into EBRs in MasterControl MES utilizing existing functionality Ability to work with site SMEs to turn existing EBRs in legacy systems (P2C2| PMX| etc.) into MasterControl MES EBRs utilizing existing functionality Ability to design Building Blocks that can be reused in multiple processes Ability to author requirements| SPEC| and validation documents Ability to test an EBR full functionality in a compliant manner
Ability to work in a fast paced agile team environment
Participates in fit gap analysis Process Modeling process standardization with Area lead Process SME
Works with lead RA to develop BB requirements
Provide times| user story point estimates| and status for all stories assigned to them Authors and performs documents supporting validation of EBRs Configures EBR in Development| Stage| Production Environment Address Site specific questions| use cases and ER from Site EBR and POWorks across the teams to put requirement together for ER development
Provide HyperCare and Go-live support
Essential Skills: Master Control MES Understanding of pharmaceutical manufacturing processes (Solid oral dose and packaging preferred) Possesses expertise in Good Documentation and Good Testing Practices
Ability to process map site requirements using Microsoft Visio or alike software
Ability to work with site SMEs to turn paper batch records into EBRs in MasterControl MES utilizing existing functionality Ability to work with site SMEs to turn existing EBRs in legacy systems (P2C2| PMX| etc.) into MasterControl MES EBRs utilizing existing functionality Ability to design Building Blocks that can be reused in multiple processes Ability to author requirements| SPEC| and validation documents Ability to test an EBR full functionality in a compliant manner
Ability to work in a fast paced agile team environment
Participates in fit gap analysis Process Modeling process standardization with Area lead Process SME
Works with lead RA to develop BB requirements
Provide times| user story point estimates| and status for all stories assigned to them Authors and performs documents supporting validation of EBRs Configures EBR in Development| Stage| Production Environment Address Site specific questions| use cases and ER from Site EBR and POWorks across the teams to put requirement together for ER development
Provide HyperCare and Go-live support
SYSMIND LLC is an Equal Employment Opportunity employer. All qualified applicants will receive consideration for employment without any discrimination. We promote and support a diverse workforce at all levels in the company. All job offers are contingent upon completion of a satisfactory background check and reference checks. Additionally passing the drug test may also be required. All contractors intending to work on SYSMIND's W2 are "at will" employees.
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