Job description
Duties & Responsibilities:
- Extracting important data from P&IDs, wiring diagrams, SOPs, Control Philosophy, and related documentation for project execution.
- Write design documents such as FDS, DDS, test plans, and test cases.
- Work with global software team members to ensure we craft and deliver quality software.
- Write internal test documents and execute structural testing.
- Provide accurate estimates for completing planned tasks and software development with the highest quality.
- Establishes and maintains detailed and accurate documentation of all work.
- Should be able to implement, document, and maintain the SCADA/MES application according to the design documents.
- Assist in acquiring information for architecture specs, software compatibility, security, and other application requirements.
Minimum Qualifications / Experience / Required Skills:
Bachelors/ master's degree in electrical / electronic / instrumentation engineering with 5 to 8 years of DCS/PLC/SCADA Development experience.
- Strong Process Automation project & commissioning experience with the Siemens/Rockwell PLC platform in a Pharma/Biotech environment.
- Knowledge of ISA 88, FDA regulations, particularly 21 CFR part 11, GMP and GAMP systems.
- Strong experience in conducting FAT, SAT and UAT activities for software and equipment.
- Rockwell-Studio5000 /Siemens PLC- Step7/ PCS7, Ignition SCADA
- Experience with Python scripting is must.
- Familiarity with upstream and downstream bioprocesses.
- Communication / Network Protocols – OPC, Modbus, Profibus, Ethernet/IP etc. Knowledge / working experience on MQTT, Traceability etc. will be added advantage.
- Exposure to development environments like GitHub, Version Control. DevOps etc.
- Willing to learn and improve technical capabilities.
