TM - Process Maintenance Instrumentation

Good Health Can’t Wait

We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.

For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).

‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency

Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.

Job Summary

1. 1. Responsible for Breakdown maintenance, Preventive maintenance, Modification and improvements, Spares Management for all process equipment, Laboratory Equipments,

1. 1. Handling Engineering & Maintenance at Process area (Production equipment & Pilot plant equipment), Laboratory equipment, Analytical equipment, Warehouse equipment, Solvent Bulk Storage & Distribution system, Electrical maintenance, including responsible for AMCs & CAMCs.

1. 1. Responsible for maintenance of UPS, system, Drying ovens, Vacuum ovens, Glassware washing machines, Muffle furnace, HPHV Steam sterilizers, De-contamination autoclaves, Air curtains, Sliding doors, Lighting devices. Gas generators (N2,O2,H2), Gas Cylinder banks & GC distribution lines.

1. 1. Responsible for maintenance of Sampling booth conveyor, Material handling equipment.

1. 1. Responsible for Preparation & Review of URS (User requirement specification), P&ID (Piping & instrumentation diagram) and PFD (Process flow diagram), BOQ (Bill of Quantity doc), Layouts.

1. 1. Responsible for preparation of Budgetary document, Capex proposal, Project schedule/Gantt chart, Schedule tracking, Enquiry processing, Order processing & Site Execution

1. 1. Responsible for Pre installation requirements of newly procured process & Laboratory equipment, Analytical equipment. Responsible for facility, equipment, system Installation, Commissioning, Validation activities.

1. 1. Responsible for review and approval of change notifications initiated in engineering systems & procedures.

1. 1. Responsible for Preparation & Review Design qualification(DQ), PSQP (Project specific quality plan), MOC assessment, Commissioning checklist, Installation Qualification (IQ), Operational qualification (OQ), PSSR (Pre start up safety assessment) & Supporting for Performance Qualification (PQ)

1. 1. Responsible for guidance and support of calibration activities of measuring devices.

1. 1. Coordinating GxP related activity, execution & review of validation activity and providing inputs requires for preparation of SOP's related with engineering systems

1. 1. Suggestion and implementation of cost effective modifications in existing systems/ equipment for improvement in process/ productivity with Quality. Inventory Management to ensure the down time is very minimum. Responsible for ensuring compliance in engineering processes, practices followed, addressing the deviations from regulatory requirements/audit observations. All time readiness for audits.

1. 1. To conduct effective investigations of notifications as an investigator. Monitor the investigation related analysis to produce the consistent results

1. 1. To ensure the appropriate CAPA shall be given to prevent the reoccurrences.

1. 1. Responsible for WPM authorization, SOI audits, PSM audits, PHA assessments, CSFA audits & Contractor safety management.

1. 1. Installation, commissioning and validation of the validation activities of computerized systems as per the Master Validation Plan

1. 1. Implementation & execution of all machinery software's (Industrial PC's, SCADA's, DAS Systems) backup's and updating of backup whenever there is a modification.

1. 1. Technical support for verification of compliance & GxP requirements of Water system DAS, Solvent Handling System, L2 integration, EMS, BMS systems.

1. 1. Technical support for execution of GxP controls in process HMIs, Industrial PCs by putting new systems in place.

Qualifications

Educational qualification

Additional Information

About the DepartmentGlobal Manufacturing Organisation (GMO)