Delta V Systems Programmer

Anter Consulting

Singapore

On-site

SGD 120,000 - 180,000

Full time

2 days ago
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Job summary

Anter Consulting is seeking a DeltaV System Programmer to lead software architecture, configuration and CSV of Emerson DeltaV DCS and PLC systems. You will ensure automated logic meets process requirements and strict global regulatory standards, including GAMP 5 and 21 CFR Part 11.

You will also act as the SME for software validation, ensuring all automated systems stay compliant, secure and audit-ready.

Qualifications

  • Degree in Computer Science, Software Engineering or Instrumentation & Control.
  • 6+ years in GMP-regulated pharma or biotech environment.
  • Expert-level experience in Emerson DeltaV, Siemens TIA Portal or Allen-Bradley RSLogix.
  • Deep knowledge of the GAMP 5 lifecycle and 21 CFR Part 11.
  • Strong analytical mindset.
  • Ability to explain complex software logic to non-technical stakeholders.

Responsibilities

  • Lead software design and data source configuration for DeltaV systems.
  • Own DeltaV batch execution, S88 recipe authoring and equipment module logic.
  • Act as the SME for software validation.
  • Author and execute lifecycle documents, including URS, FS, DS and IQ/OQ/PQ protocols.
  • Manage data flow between DeltaV and LIMS, SAP and IP.21.
  • Build connectivity using OPC UA/DA and ODBC interfaces.
  • Perform code reviews and audit trail analysis.
  • Lead investigations into software-related deviations and implement CAPA.
  • Ensure automated systems comply with data integrity (ALCOA+) principles.
  • Apply cybersecurity protocols for industrial control systems.

Skills

DeltaV systems
GAMP 5
21 CFR Part 11
Software validation
Data integrity ALCOA+
Cybersecurity for ICS
OPC UA/DA
LIMS/SAP/IP.21 data flow

Education

Degree in Computer Science or Software Engineering or Instrumentation & Control

Tools

OPC UA/DA
ODBC interfaces
IP.21 (AspenTech)

Job description

Job Description

We are hiring a DeltaV System Programmer to lead the software architecture, configuration and computerized system validation (CSV) of site-wide Emerson DeltaV DCS and PLC systems. In this role, you will make sure automated software logic meets both process requirements and strict global regulatory standards, including GAMP 5 and 21 CFR Part 11.

You will also act as the subject matter expert (SME) for software validation. As a result, every automated system stays compliant, secure and audit-ready.

Key Responsibilities
  • Lead software design and data source configuration for DeltaV systems
  • Own DeltaV batch execution, S88 recipe authoring and equipment module logic
  • Act as the SME for software validation
  • Author and execute lifecycle documents, including URS, FS, DS and IQ/OQ/PQ protocols
  • Manage data flow between DeltaV and LIMS, SAP and AspenTech InfoPlus.21 (IP.21)
  • Also build connectivity using OPC UA/DA and ODBC interfaces
  • Perform code reviews and audit trail analysis
  • Lead investigations into software-related deviations and, as a result, implement CAPA (corrective and preventive actions)
  • Ensure automated systems comply with data integrity (ALCOA+) principles
  • Finally, apply cybersecurity protocols for industrial control systems
  • Lead software design and data source configuration for DeltaV systems
  • Own DeltaV batch execution, S88 recipe authoring and equipment module logic
  • Act as the SME for software validation
  • Author and execute lifecycle documents, including URS, FS, DS and IQ/OQ/PQ protocols
  • Manage data flow between DeltaV and LIMS, SAP and AspenTech InfoPlus.21 (IP.21)
  • Also build connectivity using OPC UA/DA and ODBC interfaces
  • Perform code reviews and audit trail analysis
  • Lead investigations into software-related deviations and, as a result, implement CAPA (corrective and preventive actions)
  • Ensure automated systems comply with data integrity (ALCOA+) principles
  • Finally, apply cybersecurity protocols for industrial control systems
Required Qualifications and Skills
  • Degree in Computer Science, Software Engineering or Instrumentation & Control
  • 6+ years in a GMP-regulated pharma or biotech environment
  • Expert-level experience in Emerson DeltaV, Siemens TIA Portal or Allen-Bradley RSLogix
  • Deep knowledge of the GAMP 5 lifecycle and 21 CFR Part 11
  • Strong analytical mindset
  • In addition, the ability to explain complex software logic to non-technical stakeholders

Reference no.: 122-4948-2918-NW

Registration no.: 968446516E

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