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About the role
As a Calibration Engineer, you will be responsible for executing calibration activities for field instruments in a pharmaceutical manufacturing environment. Your key responsibilities will include: - Preparing and maintaining calibration schedules according to the calibration Master plan. - Ensuring calibration compliance of GMP critical instruments within specified due dates. - Performing troubleshooting and preventive maintenance of instrumentation systems and process control equipment. - Coordinating with Production, QA, and Engineering teams during breakdowns, shutdowns, and qualification activities. - Maintaining calibration records, certificates, instrument history cards, and documentation as per GMP requirements. - Handling PLC, SCADA, and HMI related troubleshooting and coordinating with vendors when necessary. - Ensuring compliance with cGMP, safety procedures, and regulatory requirements. - Coordinating with external calibration agencies and verifying calibration reports/certificates. - Participating in deviation investigation, CAPA implementation, change control, and audit preparation activities. - Maintaining spare parts inventory and ensuring availability of critical instrumentation spares. - Supporting energy-saving and continuous improvement initiatives related to instrumentation and automation systems. Skills required for this role include: - Knowledge of calibration standards and practices - Understanding of PLC SCADA, HMI, and automation systems - Knowledge of GMP documentation and regulatory compliance - Familiarity with Utility systems such as HVAC, Chillers, Boilers, Compressors, and water systems - Good communication and coordination skills - Basic knowledge of 21CFR Part11 In terms of qualifications, you should have a Bachelor's Degree, Diploma, B.E., or B.Tech in Instrumentation Engineering. Additionally, you should have 3 to 5 years of experience in pharmaceutical, API, injectable, OSD, or regulated manufacturing industries. As a Calibration Engineer, you will be responsible for executing calibration activities for field instruments in a pharmaceutical manufacturing environment. Your key responsibilities will include: - Preparing and maintaining calibration schedules according to the calibration Master plan. - Ensuring calibration compliance of GMP critical instruments within specified due dates. - Performing troubleshooting and preventive maintenance of instrumentation systems and process control equipment. - Coordinating with Production, QA, and Engineering teams during breakdowns, shutdowns, and qualification activities. - Maintaining calibration records, certificates, instrument history cards, and documentation as per GMP requirements. - Handling PLC, SCADA, and HMI related troubleshooting and coordinating with vendors when necessary. - Ensuring compliance with cGMP, safety procedures, and regulatory requirements. - Coordinating with external calibration agencies and verifying calibration reports/certificates. - Participating in deviation investigation, CAPA implementation, change control, and audit preparation activities. - Maintaining spare parts inventory and ensuring availability of critical instrumentation spares. - Supporting energy-saving and continuous improvement initiatives related to instrumentation and automation systems. Skills required for this role include: - Knowledge of calibration standards and practices - Understanding of PLC SCADA, HMI, and automation systems - Knowledge of GMP documentation and regulatory compliance - Familiarity with Utility systems such as HVAC, Chillers, Boilers, Compressors, and water systems - Good communication and coordination skills - Basic knowledge of 21CFR Part11 In terms of qualifications, you should have a Bachelor's Degree, Diploma, B.E., or B.Tech in Instrumentation Engineering. Additionally, you should have 3 to 5 years of experience in pharmaceutical, API, injectable, OSD, or regulated manufacturing industries.
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