IP21 Engineer at Advanced Manufacturing Tech Solutions (AMTSOL)
Singapore, , Singapore -
Full Time


Start Date

Immediate

Expiry Date

11 Oct, 26

Salary

0.0

Posted On

13 Jul, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Aspen IP21, OSIsoft PI, DeltaV, MES, PLC/DCS Integration, GMP, GxP, FDA 21 CFR Part 11, GAMP5, SQL, Data Visualization, System Documentation, IQ/OQ Protocols, Batch Data Analysis, Process Monitoring, Troubleshooting

Industry

Pharmaceutical Manufacturing

Description
Job Description – IP21 Engineer (Pharma, Singapore) Position Overview We are seeking an experienced IP21 Engineer to support pharmaceutical manufacturing operations in Singapore. The role focuses on OSIsoft PI / AspenTech InfoPlus.21 (IP21) historian systems, ensuring reliable data collection, integration, and compliance with GMP/GxP standards. Key Responsibilities Design, configure, and maintain Aspen InfoPlus.21 (IP21) historian systems for pharma manufacturing sites. Integrate IP21 with MES, DeltaV, PLC/DCS systems to enable seamless data flow. Develop and optimize data collection, reporting, and visualization tools for process monitoring. Support batch data analysis, audit trails, and regulatory compliance (FDA 21 CFR Part 11, GAMP5). Troubleshoot historian performance issues and provide hypercare support during commissioning. Collaborate with automation, validation, and QA teams to ensure data integrity and compliance. Prepare and maintain system documentation, SOPs, IQ/OQ protocols. Qualifications Bachelor's degree in Engineering, Computer Science, or related field. 5+ years of experience with IP21 historian systems in pharma / life sciences manufacturing. Strong knowledge of DeltaV, MES, PLC/DCS integration. Familiarity with GMP, GxP, FDA 21 CFR Part 11 compliance requirements. Experience with SQL, reporting tools, and data visualization platforms. Excellent problem-solving and communication skills.
Responsibilities
Design, configure, and maintain Aspen IP21 historian systems to ensure reliable data collection and integration within pharmaceutical manufacturing. Collaborate with automation and QA teams to maintain data integrity and regulatory compliance.
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