Jobs via Dice
A dynamic professional with proven expertise in
Siemens Opcenter Medical Devices
in Manufacturing Execution domain is required for the
MES Analyst
role. Responsibilities include designing and architecting multi-site MES Opcenter implementation based on discussion with business teams and their processes. The ideal candidate should have experience with
Siemens Opcenter MES and CAMSTAR ,
Manufacturing Consulting , and
Medical Devices . Key responsibilities: Design and architect multi-site MES Opcenter implementation based on discussion with business teams and their processes. Understand the paper Batch record and business process flow in collaboration with business SMEs. Implement and execute the shopfloor transaction using OpCenter Execution Discrete in Discrete manufacturing Industry. Author Computer System Validation (CSV) documents such as Functional Risk Assessment, Validation Plan, System Test Plan, Test Summary Reports (IQ/OQ/UAT), Validation Report, etc. Requirements: Proven expertise in
Siemens Opcenter Medical Devices
in Manufacturing Execution domain. Experience with
LOFTWARE PRISYM 360 . Expertise in high-performance, cross-functional teams developing, and supporting information systems in the Medical Device and pharmaceutical manufacturing industries. Location:
Bay Area, CA
- Locals only. Duration:
6+ Months .
#J-18808-Ljbffr
Siemens Opcenter Medical Devices
in Manufacturing Execution domain is required for the
MES Analyst
role. Responsibilities include designing and architecting multi-site MES Opcenter implementation based on discussion with business teams and their processes. The ideal candidate should have experience with
Siemens Opcenter MES and CAMSTAR ,
Manufacturing Consulting , and
Medical Devices . Key responsibilities: Design and architect multi-site MES Opcenter implementation based on discussion with business teams and their processes. Understand the paper Batch record and business process flow in collaboration with business SMEs. Implement and execute the shopfloor transaction using OpCenter Execution Discrete in Discrete manufacturing Industry. Author Computer System Validation (CSV) documents such as Functional Risk Assessment, Validation Plan, System Test Plan, Test Summary Reports (IQ/OQ/UAT), Validation Report, etc. Requirements: Proven expertise in
Siemens Opcenter Medical Devices
in Manufacturing Execution domain. Experience with
LOFTWARE PRISYM 360 . Expertise in high-performance, cross-functional teams developing, and supporting information systems in the Medical Device and pharmaceutical manufacturing industries. Location:
Bay Area, CA
- Locals only. Duration:
6+ Months .
#J-18808-Ljbffr