I am looking for Siemens Opcenter Execution Pharma Process Instructions (PIs) or POMSNet MES.
Please enable profiles for the below JD.
Start Date: 16-Mar-26
Country: Germany Italy Ireland : Candidate should be based anywhere in EU and can work remotely but needs to travel onsite 15% in a month.
Contract Duration: 12 months
Interview : 2 rounds
No of positions: 2
- System Development and Configuration: Designing configuring and testing Siemens Opcenter Execution Pharma Process Instructions (PIs) to align with site-specific manufacturing requirements.
- Electronic Batch Record (eBR) Creation: Developing and implementing eBRs to replace paper-based systems enhancing compliance and reducing review times.
- Regulatory Compliance (GxP/GMP): Ensuring all MES configurations adhere to strict regulatory standards including Good Manufacturing Practices (GMP) and 21 CFR Part 11.
- System Integration: Integrating Opcenter with enterprise systems such as SAP (ERP) LIMS and SCADA/control systems using SQL and web services.
- Validation and Documentation: Creating essential documentation including User Requirement Specifications (URS) Functional Requirement Specifications (FRS) and IQ/OQ/PQ test scripts.
- Process Optimization: Analyzing manufacturing processes to identify inefficiencies and implementing solutions to enhance productivity and traceability.
- Technical Support: Troubleshooting and providing support for Opcenter application issues including managing user access and system performance.
- Training and Mentoring: Training key users on the system creating user manuals and providing guidance to junior engineers.
Typical Qualifications & Skills:
- Experience range can be between 7 and 12 years
- Experience with Siemens Opcenter Execution Pharma (Simatic IT eBR).
- Proficiency in SQL databases and system integration technologies.
- Background in pharmaceutical manufacturing processes (cGMP) and ISA-95/ISA-88 standards.
I am looking for Siemens Opcenter Execution Pharma Process Instructions (PIs) or POMSNet MES.Please enable profiles for the below JD.Start Date: 16-Mar-26Country: Germany Italy Ireland : Candidate should be based anywhere in EU and can work remotely but needs to travel onsite 15% in a month. Contrac...
I am looking for Siemens Opcenter Execution Pharma Process Instructions (PIs) or POMSNet MES.
Please enable profiles for the below JD.
Start Date: 16-Mar-26
Country: Germany Italy Ireland : Candidate should be based anywhere in EU and can work remotely but needs to travel onsite 15% in a month.
Contract Duration: 12 months
Interview : 2 rounds
No of positions: 2
- System Development and Configuration: Designing configuring and testing Siemens Opcenter Execution Pharma Process Instructions (PIs) to align with site-specific manufacturing requirements.
- Electronic Batch Record (eBR) Creation: Developing and implementing eBRs to replace paper-based systems enhancing compliance and reducing review times.
- Regulatory Compliance (GxP/GMP): Ensuring all MES configurations adhere to strict regulatory standards including Good Manufacturing Practices (GMP) and 21 CFR Part 11.
- System Integration: Integrating Opcenter with enterprise systems such as SAP (ERP) LIMS and SCADA/control systems using SQL and web services.
- Validation and Documentation: Creating essential documentation including User Requirement Specifications (URS) Functional Requirement Specifications (FRS) and IQ/OQ/PQ test scripts.
- Process Optimization: Analyzing manufacturing processes to identify inefficiencies and implementing solutions to enhance productivity and traceability.
- Technical Support: Troubleshooting and providing support for Opcenter application issues including managing user access and system performance.
- Training and Mentoring: Training key users on the system creating user manuals and providing guidance to junior engineers.
Typical Qualifications & Skills:
- Experience range can be between 7 and 12 years
- Experience with Siemens Opcenter Execution Pharma (Simatic IT eBR).
- Proficiency in SQL databases and system integration technologies.
- Background in pharmaceutical manufacturing processes (cGMP) and ISA-95/ISA-88 standards.
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