Job Duties Outline job duties/responsibilities below: * To ensure that engineering, qualification & validation records are developed and maintained as per the c GMP and GDP requirements & SOP. * Coordination with design consultant as required and respective user department for the design of process/manufacturing equipment (Manufacturing Vessel, Blender, Filling lines etc.). * Review & approval on detailed design as submitted by vendors (e.g. Manufacturing Vessel, Blender, Filling lines etc.). * To ensure project execution work and follow-ups with different departments (QA, QM, Operations etc.) to meet the project completion within stipulated time frame. * Effectively communicate & discuss related to day to day activity and concerns within team for efficiency and performance improvement. * To prepare, review & update of standard operating procedures at regular intervals to meet c GMP requirements. * To ensure the compliance of current Good Manufacturing Practices of related process/manufacturing equipment (Manufacturing Vessel, Blender, Filling lines etc.). * To ensure that Preventive Maintenance is developed for relevant equipment/processes in co-ordination with the relevant departments as per schedule. * Responsible for development, execution and review of Qualification / Re-Qualification and Validation activity of related process/manufacturing equipment (Manufacturing Vessel, Blender, Filling lines etc.) * To ensure the compliance of Engineering Department activities as per Quality management system. * Review & verification of Engineering department standard operating procedures at regular intervals to meet c GMP & Regulatory requirements. * To carry out FAT/SAT activities as required for newly installed equipment/Systems. * Installation and Operational qualification activity of related process/manufacturing equipment (Manufacturing Vessel, Blender, Filling lines etc.). * To ensure the calibration of relevant Engineering Department instruments are performed as per validation requirements and documented as required per c GMP requirements. * To ensure that all Engineering changes are assessed and implemented as per c GMP and local SOP. For full details on this role Contact Skills: process engineer engineering pharma