DeltaV GMP Automation Engineer 6-Month Contract

LEGATUS FORMWORKS PTE LTD; Singapore; On-site; SGD 90,000 - 130,000; Part time

Job summary

LEGATUS FORMWORKS PTE LTD is seeking a DeltaV systems specialist to oversee operation, maintenance, and continuous improvement of DeltaV (DCS) for GMP-compliant pharmaceutical processes. The role includes DS computerized system administration, access reviews, data backup, and time synchronization.

You will support lifecycle activities such as change control, deviation investigations, CAPA, qualification/validation, and GMP releases, ensuring regulatory compliance and data integrity.

Qualifications

• DeltaV system expertise and operation.
• Knowledge of data integrity and 21 CFR Part11 requirements.
• Familiarity with DS equipment and instrumentation.
• Minimum of five years in pharma with at least three years in DeltaV/computerized system management.

Responsibilities

• Participate in operation, maintenance, troubleshooting, and continuous improvement of DeltaV (DCS) to ensure system reliability, availability, and GMP compliance.
• Administer DS computerized systems, including user management, access reviews, data backup/recovery, and time synchronization.
• Support system lifecycle activities: change control, deviation investigation, CAPA, qualification/validation, and GMP release for regulatory compliance and data integrity.
• Provide technical support to manufacturing operations, troubleshoot automation issues, coordinate with vendors and cross-functional teams, and drive continuous improvement initiatives.

Skills

DeltaV system

Data Integrity & 21 CFR Part11

DS equipment & instrument

Pharmaceutical industry experience

Tools

Emerson DeltaV

Job description

LEGATUS FORMWORKS PTE LTD is seeking a DeltaV systems specialist to oversee operation, maintenance, and continuous improvement of DeltaV (DCS) for GMP-compliant pharmaceutical processes. The role includes DS computerized system administration, access reviews, data backup, and time synchronization.

You will support lifecycle activities such as change control, deviation investigations, CAPA, qualification/validation, and GMP releases, ensuring regulatory compliance and data integrity.