Lead Design Review ( Electrical and Instrumentation ) Fresher's job
1 year ago Public Service Hyderabad 78 views Reference: 30132Job Details
| PURPOSE | ||||||||
| 1. To follow up with consultants to get the details, design, and with SCM for PO release in time to meet the overall time line of the project. 2. To ensure release of construction drawings and design of the assigned projects in order to meet Project scope, Schedule and Cost. 3. To Review the design, drawing, and BOQ released by consultant against the requirement and expectations . 4. Collaborate across organization with various stakeholders from time to time to meet the requirements and expectations. 5. Identify and act to manage project risks effectively. 6. To manage project execution | ||||||||
| Within: Biologics unit of Dr.Reddy's Laboratories | ||||||||
| With the objective of: Timely delivery of Capital Projects which will enable organization in capacity/capability building, product launches, Cost optimisation initiatives etc. | ||||||||
| Design Review |
| Reviewing the design documents, construction drawing (Layout / PID / SLD ) to meet the URS and user expectations. Reviewing the execution plan and methodology to meet the timelines, quality and specifications. Preparing / Reviewing BOQs . Planning of resources (Manpower, tools, equipment) according to project needs and timelines. Participation in Technical Evaluation of Vendor & Equipment - in order to ensure that all contributory factors and reasonable design options have been considered, and that the design meets the requirements as outlined, |
| Project execution |
| Indenting of material & following -up with supply chain for delivery of material, Responsible for monitoring the progress of the projects execution as per the timelines & Quality checks. Managing contractors, Responsible for safety and regulatory standards compliances, Issuing of Safety Permits, conducting Tool Box Talks in order to carry out the work in the project scope, coordinating the team's work, acting in real-time to course-correct if the project runs into difficulty. |
| Safety Compliance |
| 100% safety compliance by ensuring safety measures and procedure compliances are in place, continuous training & its effective implementation on safety standards and procedures, regular review of safety dash board for the function and initiatives to improve safety compliances. In order to timely support business requirements/goals |
| Ensuring regulatory compliances |
| Ensuring statutory compliance like - DOF, HMDA, IBR , Environment, NBC ect.. |
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Company Description
Dr. Reddy's Laboratories is an Indian multinational pharmaceutical company based in Hyderabad. The company was founded by Kallam Anji Reddy, who previously worked in the mentor institute Indian Drugs and Pharmaceuticals Limited.[2] Dr. Reddy's manufactures and markets a wide range of pharmaceuticals in India and overseas. The company has over 190 medications, 60 active pharmaceutical ingredients (APIs) for drug manufacture, diagnostic kits, critical care, and biotechnology.
Dr. Reddy's began as a supplier to Indian drug manufacturers, but it soon started exporting to other less-regulated markets that had the advantage of not having to spend time and money on a manufacturing plant that would gain approval from a drug licensing body such as the U.S. Food and Drug Administration (FDA). By the early 1990s, the expanded scale and profitability from these unregulated markets enabled the company to begin focusing on getting approval from drug regulators for their formulations and bulk drug manufacturing plants in more-developed economies. This allowed their movement into regulated markets such as the US and Europe. In 2014, Dr. Reddy Laboratories was listed among 1200 of India's most trusted brands according to the Brand Trust Report 2014, a study conducted by Trust Research Advisory, a brand analytics company.[3]
By 2007, Dr. Reddy's had seven FDA plants producing active pharmaceutical ingredients in India and seven FDA-inspected and ISO 9001 (quality) and ISO 14001 (environmental management) certified plants making patient-ready medications five of them in India and two in the UK.[4]
Dr. Reddy's began as a supplier to Indian drug manufacturers, but it soon started exporting to other less-regulated markets that had the advantage of not having to spend time and money on a manufacturing plant that would gain approval from a drug licensing body such as the U.S. Food and Drug Administration (FDA). By the early 1990s, the expanded scale and profitability from these unregulated markets enabled the company to begin focusing on getting approval from drug regulators for their formulations and bulk drug manufacturing plants in more-developed economies. This allowed their movement into regulated markets such as the US and Europe. In 2014, Dr. Reddy Laboratories was listed among 1200 of India's most trusted brands according to the Brand Trust Report 2014, a study conducted by Trust Research Advisory, a brand analytics company.[3]
By 2007, Dr. Reddy's had seven FDA plants producing active pharmaceutical ingredients in India and seven FDA-inspected and ISO 9001 (quality) and ISO 14001 (environmental management) certified plants making patient-ready medications five of them in India and two in the UK.[4]
