GMP Automation Engineer (9-Month Pharma Contract)

RECRUIT EXPRESS PTE LTD; Singapore; On-site; SGD 81,000 - 97,000; Full time

Job summary

RECRUIT EXPRESS PTE LTD seeks an experienced Automation/QA Engineer to maintain GMP computerized systems at a Joo Koon facility on a 9-month contract. You will ensure validated state, manage access controls, alarm audits, and support qualification activities.

The role requires 5+ years in pharma/regulatory manufacturing, PL C/SCADA hands-on skills, and familiarity with Rockwell, Siemens, WinCC, Historian, and Active Directory. Strong data integrity & GMP knowledge are essential.

Qualifications

• Minimum degree in Automation, Electrical/Electronics, Instrumentation or Computer Engineering.
• At least 5 years of experience in pharmaceutical or regulated manufacturing.
• Hands-on PLC/SCADA experience in sterile manufacturing.
• Familiar with Rockwell FactoryTalk, Siemens TIA Portal, WinCC, Historian and Active Directory.
• Knowledge of GMP, data integrity and ALCOA+ requirements is preferred.

Responsibilities

• Maintain GMP computerized systems in validated state.
• Perform user-access, alarm, audit-trail and periodic reviews.
• Support data backup, restoration testing and security-log reviews.
• Manage deviations, change controls, CAPAs and risk assessments.
• Support commissioning, qualification and validation activities.
• Provide technical support for PLC, HMI, SCADA and virtualized systems.
• Support audits and ensure compliance with GAMP 5, cGMP and ALCOA+.

Skills

PLC/SCADA systems

GAMP 5 compliance

data integrity

Active Directory

Audit & validation support

Education

Degree in Automation / Electrical / Electronics / Instrumentation / Computer Engineering

Tools

Rockwell FactoryTalk

Siemens TIA Portal

WinCC

Historian

Maximo

TrackWise

Kneat

Active Directory

Job description

RECRUIT EXPRESS PTE LTD seeks an experienced Automation/QA Engineer to maintain GMP computerized systems at a Joo Koon facility on a 9-month contract. You will ensure validated state, manage access controls, alarm audits, and support qualification activities.

The role requires 5+ years in pharma/regulatory manufacturing, PL C/SCADA hands-on skills, and familiarity with Rockwell, Siemens, WinCC, Historian, and Active Directory. Strong data integrity & GMP knowledge are essential.