Team Member - Engineering ( Process Maintenance – Instrumentation)

Job Summary
We are looking for a detail-oriented engineering team member to coordinate preventive maintenance schedules manage breakdown records and ensure adherence to SOPs critical for maintaining operational efficiency and equipment reliability. This role plays a pivotal part in inventory control and CAPA closure contributing to seamless production operations compliance with regulatory standards and effective resource utilization.

Roles & Responsibilities
You will be responsible for coordinating with cross functional teams for ensuring that preventive maintenance is carried out as per schedules in SAP.
Your role involves preparing the PMP (Preventive Maintenance Plan) and maintaining the necessary records of breakdowns and maintenance activities in the PMP as per defined frequency.
Your responsibilities include handling of external contractors and agencies reviewing and ensuring implementation of the instructions (Work Instructions and SOPs Standard Operating Procedures) related to production operation.
You will train and assist the team members during troubleshoot and breakdown of machines and commissioning of new Equipment.
You will ensure balance investigation and inventory control for all instrument spares parts.
Your role involves planning consolidating and submitting the maintenance budget for the allotted area/unit.
You will ensure that the maintenance expense is within the budgeted amount.
You will be responsible for ensuring availability of all process equipment and regular maintenance of all process equipment spares by following up with OEMs (Original Equipment Manufacturers) external vendors and SCM (Supply Chain Management).
You will be accountable for enduring closure and completion all assigned CAPA (Corrective and Preventive Actions) on time.
You will be expected to support any technical/documentation activities at site as per instructions from Section Head.
You will be responsible for preparing updating and maintaining all necessary documents for audits like SOPs formats PM (Preventive Maintenance) books protocols and Machine History Books for the respective areas.
Your responsibilities include facility upkeep of respective areas as per GMP (Good Manufacturing Practices) and cGMP (Current GMP).
You will be accountable for ensuring implementation of Good Engineering Practices (GEP) at Site.

Qualifications :

Edu : Diploma in Electrical & Instrumentation Engineering or
B. Tech in Electrical & Instrumentation Engineering.

1. Responsible for coordinating and executing project development and handover activities of in-house projects in the plant
2. In house Project Works and coordination with vendors during projects execution.
3. Following all related SOPs PMPs & OIs and ensuring concurrent Documentation.
4. Maintenance & Machining of parts as per requirement.
5. Closing of Change Controls Job proposals Quality Non-Quality Impacting reports and cross checks
6. Guiding and controlling external vendors working inside plant and arranging required material as per technical details required for work completion.
7. Preparation of Engineering Provisions and drawings/layouts.
8. Preparation of commissioning reports for new equipment Instrument and submissions to Asset Team.
9. Coordinating with CFTs for timely project execution.
10. Training the user department and ensuring regular operation of systems implemented.
11. Coordination with service providers during installations commissioning and execution of qualification activities breakdowns of systems & equipment.
12. Technical evaluation of changes in the validated systems or processes.
13. Responsible for addressing the deviations in external/internal audit observation in engineering processes practices followed.
14. Execution Review Installation & Commissioning of new equipment along with related documentation like DQ IQ OQ PQ and related SOPs.
15. Responsible for initiation review of deviation management through incidents relevant to the in-house projects and incident investigation related to engineering.
16. To Review of SOPs and OIs coordination with QA and follow relevant SOPs.
17. To follow the quality procedures and regulatory requirements.
18. Monitoring of maintenance systems in SAP
19. Responsible for planning of preventive maintenance
20. Operation and Maintenance of pure steam generators.
21. Responsible for taking the Periodic GXP Computerized system backup and submitting to IT department.
22. Technical support to carry out the GxP assessment & controls for manufacturing machines.
23. Good knowledge on PLC Programming.

Additional Information :

About the Department
Global Manufacturing Organisation (GMO)
At Dr. Reddys Laboratories we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence we are a leading force in the pharmaceutical industry.
We operate 19 state-of-the-art manufacturing plants across Hyderabad Vizag Baddi Mexico Shreveport and Mirfield comprising 8 OSD facilities 3 Injectables facilities and 8 API facilities.
Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1150 drug master files across key therapy areas such as Oncology Cardio-vascular Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally Hyderabad as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive meeting business imperatives and meeting our ambitious ESG goals. Building such factories of the future is integral to innovation and to build healthcare of the future.

Benefits Offered
At Dr. Reddys we actively help to catalyse your career growth and professional development through personalised learning programs.
The benefits you will enjoy at Dr. Reddys are on par with the best industry standards. They include among other things and other essential equipment joining & relocation support family support (Maternity & Paternity benefits) learning and development opportunities medical coverage for yourself and your family life coverage for yourself.

Our Work Culture
Ask any employee at Dr. Reddys why they come to work every day and theyll say because Good Health Cant Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations but as a means to help patients lead healthier lives and were always attuned to the new and the next to empower people to stay fit. And to do this we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system they can make magic.
For more details please visit our career website at Work :

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