Team Member

2 weeks ago

Visakhapatnam, India Dr Reddy's Laboratories Limited Full time

**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.
**Job Description** Job Summary**

**Roles & Responsibilities**
- Follow and adhere to the SOP’s and other laid down the procedure in the production
- Follow and adhere to the company safety norms, company policies and procedures in the departments.
- To ensure effective implementation of Company policies and Procedures in the departments.
- Initiation of Quality notification, breakdown notification and change control in SAP.
- Preparation and review of investigation report.
- Initiation and closure of CAPA as per procedure.
- Review and Approval of SOP, URS, Protocols, reports in DOCHUB.
- Review and Approval of workflow, recipe and eBMR in MES.
- Conduct group discussion related to incident investigation to find the cause of discrepancy.
- Participate, Preparation and review of Risk assessments.
- To review and approve Validation, Qualification Documents and related reports as per requirement.
- Preparation and Review of alarm trending of equipment.
- To perform and review GxP assessment, system level impact assessment and CSV qualification.
- To ensure that the qualification, Validation, Calibration of equipment and process validation are done as per schedule and requirement.
- To review and approve Validation, Qualification Documents and related reports as per requirement.
- Scheduled and execution of Manufacturing plan.
- Planning of routine activities, manpower planning and work allocation for manufacturing.
- Responsible for activities like Dispensing and Manufacturing ( Blending, Granulation, Compression, Coating, Capsulation, Imprinting and Inspection ) as per Production plan.
- Coordination with operators for smooth running of manufacturing activities.
- To coordinate with the research and development and development and manufacturing sciences and technology team for planning and execution of the Exhibit Batches in the manufacturing Department.
- To ensure smooth coordination with other related departments
- Warehouse, HR, Admin, Engineering services, QA, QC, MSAT, IPDO and SHE.
- To ensure timely completion of calibration & Preventive maintenance activities of manufacturing equipment’s.
- To coordinate with engineering department to reduce manufacturing breakdown time and ensure proper rectification of the problems occurred.
- To attend inventory & production planning meeting and accordingly ensure proper material and manufacturing.
- To perform Spot checks and GEMBA walk as per schedule.
- To ensure that the required initial and periodic training of department personnel in completed as per schedule and give the training to below team members as when required.
- Review of area environment monitoring trends.
- To ensure that material indents are done as per the requirement and to review and approve the purchase indents for department.
- To prepare and circulate the Daily Production Report to HOD.
- To review the market complaints in coordination with QA Department and taking the required corrective and Preventive action.
- Review of Executed eBMR & workflows and ensure the submission to IPQA department on time.
- Review the Audit trail reports of equipment.
- To Perform any task/project assigned by HOD.
- To perform the duties of Designee for Head of the department whenever HOD is absent / busy in other activities

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