Senior Automation Engineer RJ 04/24
at No Deviation Pte Ltd
Singapore, Southeast, Singapore -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 08 Jul, 2024 | Not Specified | 09 Apr, 2024 | 10 year(s) or above | Manufacturing Processes,Presentations,Communication Skills,Schneider,Technical Writing | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Primary Tasks & Responsibilities
- Responsible for leading Pharma and Biopharma projects using DeltaV System with batch design (CM, EM, Phase, Recipe, etc).
- Responsible for design & manage interfaces to third party PLC systems with DeltaV.
- Responsible for managing internal stakeholders and coordination with various system vendors.
- Responsible for reviewing vendor functional specifications and design specifications and ensuring these are aligned with client global and local standards.
- Work with various teams to design system architecture, network architecture, cable schedule.
- Responsible for reviewing test documents and protocols (FAT, SAT, Interface Test, etc.) so that they meet CSV and QA standards.
- Responsible for participating in design meetings at various vendor locations.
- Responsible for witnessing FAT’s and interface test at various vendor locations.
- Work closely with qualification teams to support qualification test generation and execution efforts in IQ, OQ and PQ.
- Support FAT, SAT, IQ, OQ and PQ.
Required Experience & Knowledge
- 10+ years of experience in executing DeltaV Pharma & Biopharma Batch projects.
• Extensive knowledge of DeltaV Batch is required. • Understanding of S88 standard is required.
- Good understanding of the vaccine manufacturing processes or similar such processes is required.
- Understanding of PLC systems like Siemens, Schneider, Rockwell with some prior execution experience in interfacing these systems to DeltaV is required.
- Experienced in developing automation design philosophies, test plans, protocols and quality reports.
- Experienced in developing automation URS, FS, DS from process writeups and tech transfer documents.
- Proficiency in written and verbal communication skills (including technical writing and presentations) with ability to communicate and collaborate effectively with other stakeholders.
Responsibilities:
- Responsible for leading Pharma and Biopharma projects using DeltaV System with batch design (CM, EM, Phase, Recipe, etc).
- Responsible for design & manage interfaces to third party PLC systems with DeltaV.
- Responsible for managing internal stakeholders and coordination with various system vendors.
- Responsible for reviewing vendor functional specifications and design specifications and ensuring these are aligned with client global and local standards.
- Work with various teams to design system architecture, network architecture, cable schedule.
- Responsible for reviewing test documents and protocols (FAT, SAT, Interface Test, etc.) so that they meet CSV and QA standards.
- Responsible for participating in design meetings at various vendor locations.
- Responsible for witnessing FAT’s and interface test at various vendor locations.
- Work closely with qualification teams to support qualification test generation and execution efforts in IQ, OQ and PQ.
- Support FAT, SAT, IQ, OQ and PQ
REQUIREMENT SUMMARY
Min:10.0Max:15.0 year(s)
Information Technology/IT
IT Software - QA & Testing
Software Testing
Graduate
Proficient
1
Singapore, Singapore