Develop Pharmaceutical SCADA Application in COPA-DATA zenon (21 CFR Part 11)
Budget: ₹12,500 – ₹37,500 INR
We are looking for an experienced COPA-DATA zenon SCADA developer for a pharmaceutical automation project.
The project involves upgrading an existing HMI system to a zenon SCADA solution with support for FDA 21 CFR Part 11 compliance.
Scope of Work:
• Develop a zenon SCADA application from project specifications.
• Configure communication with the existing PLC.
• Design professional SCADA screens.
• Configure alarms, trends, and historical data.
• Implement user management and role-based access.
• Configure audit trail and electronic signatures.
• Configure recipe management (if required).
• Generate reports and event logs.
• Support FAT and debugging.
• Provide complete project source files and documentation.
Required Skills:
• Strong experience with COPA-DATA zenon Engineering Studio.
• Experience in pharmaceutical or GMP-regulated industries.
• Knowledge of FDA 21 CFR Part 11 and audit trail implementation.
• Experience with PLC communication (Siemens, Allen Bradley, Beckhoff, etc.).
• Experience configuring alarms, historian, user management, and reports.
Preferred:
• Previous pharmaceutical SCADA projects.
• Experience implementing electronic signatures and audit trails in zenon.
• Ability to provide references or screenshots of similar projects.
Please Include in Your Proposal:
• Years of experience with zenon.
• Number of zenon projects completed.
• Experience with 21 CFR Part 11 projects.
• Relevant project examples or screenshots.
• Estimated availability.
• Hourly rate or fixed-price proposal.
Important:
Preference will be given to freelancers who have already completed similar zenon SCADA projects in pharmaceutical or regulated industries. Please mention your relevant experience in your proposal.
The project involves upgrading an existing HMI system to a zenon SCADA solution with support for FDA 21 CFR Part 11 compliance.
Scope of Work:
• Develop a zenon SCADA application from project specifications.
• Configure communication with the existing PLC.
• Design professional SCADA screens.
• Configure alarms, trends, and historical data.
• Implement user management and role-based access.
• Configure audit trail and electronic signatures.
• Configure recipe management (if required).
• Generate reports and event logs.
• Support FAT and debugging.
• Provide complete project source files and documentation.
Required Skills:
• Strong experience with COPA-DATA zenon Engineering Studio.
• Experience in pharmaceutical or GMP-regulated industries.
• Knowledge of FDA 21 CFR Part 11 and audit trail implementation.
• Experience with PLC communication (Siemens, Allen Bradley, Beckhoff, etc.).
• Experience configuring alarms, historian, user management, and reports.
Preferred:
• Previous pharmaceutical SCADA projects.
• Experience implementing electronic signatures and audit trails in zenon.
• Ability to provide references or screenshots of similar projects.
Please Include in Your Proposal:
• Years of experience with zenon.
• Number of zenon projects completed.
• Experience with 21 CFR Part 11 projects.
• Relevant project examples or screenshots.
• Estimated availability.
• Hourly rate or fixed-price proposal.
Important:
Preference will be given to freelancers who have already completed similar zenon SCADA projects in pharmaceutical or regulated industries. Please mention your relevant experience in your proposal.