A dedicated and detail-oriented Process Instrumentation Engineer with hands-on experience in pharmaceutical manufacturing environments. Skilled in maintenance, and troubleshooting of field instruments and control panels, with exposure to automation systems including PLC, SCADA, and HMI (Siemens, Allen Bradley, Delta, Mitsubishi). Experienced in handling GMP documentation, change controls, deviations, and CAPAs. Proficient in using SAP and AMPLE applications for maintenance. Strong team player with a commitment to ensuring operational reliability and regulatory compliance.
➢ Performing preventive and corrective maintenance for uninterrupted plant operations.
➢ Attending and resolving instrumentation breakdowns to minimize process downtime.
➢ Hands-on with PLCs, SCADA systems, and VFDs for efficient process control and monitoring.
➢ Actively participated in regulatory/internal audits; ensured documentation as per GMP standards.
➢ Coordinated with production, QA, and validation teams for timely resolution of instrumentation issues.
➢ Supported new equipment installations and instrumentation modifications as per SOPs and GMP.
➢ Handled documentation and implementation of Change Controls for instrument modifications.
➢ Participated in investigation and closure of Deviations related to instrumentation failures.
➢ Executed CAPAs to address root causes and improve system reliability and compliance.
➢ Good exposure to maintenance and troubleshooting of different pharmaceutical equipment’s
➢ Troubleshooting of control system issues, as well as Attending to Breakdowns and Maintaining of Process Equipment's.
➢Hands-on experience with PLCs, as well as Beijer HMIs and VFDs, contributing to effective process control and automation.
➢ Responsible for identifying and Trouble shooting of field instruments/system faults and updating to manager on the status of work activities and reporting any abnormalities or incidents as required.
Executing the qualification of process equipment as per the project plan, and attending requalification activities for process equipment as per schedule.
Coordinate effectively with other departments in investigating equipment or instrument failure, and make appropriate recommendations in a timely manner for the efficient completion of work.
➢Used SAP for managing maintenance orders, tracking equipment history, and inventory management.
➢ Worked with AMPLE application for managing documentation, and compliance reports.
➢Automation Systems:
➢Programming: Basic PLC and HMI programming knowledge
➢Pharma Compliance: GMP, SOPs, Change Controls, Deviations, CAPA handling, Audit readiness
➢Software: SAP PM, AMPLE application for maintenance documentation
➢Teamwork and documentation: cross-functional coordination, technical reporting, and GMP documentation