Requirements:
- 5+ years of experience in automation engineering within the pharmaceutical or biopharmaceutical industry.
- Proven experience in designing and commissioning Emerson DeltaV DCS projects for GMP manufacturing sites.
- Strong knowledge of Batch S88 standards (CM, EM, Phases, Recipes, Units).
- Understanding of pharmaceutical/biopharmaceutical manufacturing processes, automation hardware, and networking technologies.
- Familiarity with SDLC and pharma quality management processes.
- Strong communication and coordination skills with multi-disciplinary teams.
- Ability to work onsite in Singapore.
Roles & Responsibilities:
- Design, develop, and provide commissioning support for Pharmaceutical DeltaV DCS systems on site.
- Participate in the development and implementation of automation solutions in line with ISA S88 standards.
- Develop Physical and Procedural Layer designs, perform system architecture planning, create design specifications, control strategies, and library development.
- Provide day-to-day support for DeltaV systems in manufacturing operations.
- Conduct root cause analysis for NCs and CAPAs, and drive continuous improvement initiatives.
- Execute field commissioning of automation equipment and perform system administration/maintenance.
- Support computer system validation (CSV) and documentation for automation systems.
- Collaborate with Operations, Process, and Equipment Vendor teams, as well as technology providers.
