Team Member - Engineering at Dr Reddy's Laboratories Limited

Hyderabad, Telangana, India -

Full Time

Start Date

Immediate

Expiry Date

09 Jul, 26

Salary

0.0

Posted On

10 Apr, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Preventive maintenance, Breakdown maintenance, Equipment validation, Inventory control, CAPA management, SOP compliance, Engineering documentation, Project scheduling, Calibration support, Mechanical maintenance, GMP, GEP, Troubleshooting, Budget management, Regulatory compliance, Technical documentation

Industry

Pharmaceutical Manufacturing

Description

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because 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 Description 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 Responsible for Breakdown maintenance, Preventive maintenance, Modification and improvements, Spares Management for all process equipment, Laboratory Equipments, 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. 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. Responsible for maintenance of Sampling booth conveyor, Material handling equipment. 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. Responsible for preparation of Budgetary document, Capex proposal, Project schedule/Gantt chart, Schedule tracking, Enquiry processing, Order processing & Site Execution Responsible for Pre installation requirements of newly procured process & Laboratory equipment, Analytical equipment. Responsible for facility, equipment, system Installation, Commissioning, Validation activities. Responsible for review and approval of change notifications initiated in engineering systems & procedures. 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) Responsible for guidance and support of calibration activities of measuring devices. Coordinating GxP related activity, execution & review of validation activity and providing inputs requires for preparation of SOP's related with engineering systems 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. To conduct effective investigations of notifications as an investigator. Monitor the investigation related analysis to produce the consistent results To ensure the appropriate CAPA shall be given to prevent the reoccurrences. Responsible for WPM authorization, SOI audits, PSM audits, PHA assessments, CSFA audits & Contractor safety management. Installation, commissioning and validation of the validation activities of computerized systems as per the Master Validation Plan 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. Technical support for verification of compliance & GxP requirements of Water system DAS, Solvent Handling System, L2 integration, EMS, BMS systems. Technical support for execution of GxP controls in process HMIs, Industrial PCs by putting new systems in place. Qualifications Educational qualification: A Diploma or a B.Tech./M.Tech. Minimum work experience: 8 to 10 years Skills & attributes: Technical Skills • Knowledge and experience in handling mechanical maintenance, preventive maintenance, equipment breakdown maintenance, and predictive maintenance. • Experience in troubleshot and breakdown management of machines and equipment. • Experience in managing preventive maintenance plans. • Ability to manage maintenance budget of an area/unit. • Knowledge of GMP and GEP. Behavioural skills • Communication and collaboration skills to coordinate with cross functional teams, external contractors and agencies. • Attention to detail to ensure preventive maintenance, documentation, and inventory control. • Commitment to quality and compliance. Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's 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 1,150+ 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. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s 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. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t 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 we’re 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 https://careers.drreddys.com/#!/ Job Family: Plant Engineering Sub Job Family: Operation, Repair & Maintenance Preferred type of working: On-Premise Business unit: GMO

Responsibilities

The role involves coordinating preventive and breakdown maintenance for various pharmaceutical manufacturing and laboratory equipment to ensure operational efficiency. It also requires managing inventory, overseeing validation activities, and ensuring strict adherence to regulatory standards and SOPs.