B. Tech Chemical Engineering Passed outs with 0-3 Yrs experienced candidates to work in Hyderabad or Visakhapatnam.

B. Tech Chemical Engineering Passed outs with 0-3 Yrs experienced candidates to work in Hyderabad or Visakhapatnam.

1. To carry out Formulation and Research activities as per department plan.2. Collection of literate related to the product from various site and to prepare summary report.3. Coordinating with the cross-functional departments such as Production, QA, QC, FAD for smooth running of the daily activities.4. Initiate stability testing of new products as per ICH guidelines.5. Executing the development of robust, stable and effective formulations and dosage form for new product development.6. Prepare specification, documentation, and reports related to product development.7. Prepare and review required FRD related documents activity like Master formula Record, Master Packing Record, PDR, logbooks and daily records.8. Prepare and review SOPs, and review appropriate documentation and test results for accuracy and completeness and compliance with SOPs/GMP requirement.9. Monitoring the qualification of department equipments and validation activities.10. To Prepare tech pack before execution of scale up and validation batches.11. Responsible for shift activities in the FRD department as per schedule and instructions given by Manager.12. Ensuring equipment preventive maintenance is done as per schedule.13. Training of personnel on Job and department related activities.14. Reporting daily activities to Manager.

B. Tech Chemical Engineering Passed outs with 0-3 Yrs experienced candidates to work in Hyderabad or Visakhapatnam.

B. Tech Chemical Engineering Passed outs with 0-3 Yrs experienced candidates to work in Hyderabad or Visakhapatnam.

B. Tech Chemical Engineering Passed outs with 0-3 Yrs experienced candidates to work in Hyderabad or Visakhapatnam.

1. To carry out Formulation and Research activities as per department plan.2. Collection of literate related to the product from various site and to prepare summary report.3. Coordinating with the cross-functional departments such as Production, QA, QC, FAD for smooth running of the daily activities.4. Initiate stability testing of new products as per ICH guidelines.5. Executing the development of robust, stable and effective formulations and dosage form for new product development.6. Prepare specification, documentation, and reports related to product development.7. Prepare and review required FRD related documents activity like Master formula Record, Master Packing Record, PDR, logbooks and daily records.8. Prepare and review SOPs, and review appropriate documentation and test results for accuracy and completeness and compliance with SOPs/GMP requirement.9. Monitoring the qualification of department equipments and validation activities.10. To Prepare tech pack before execution of scale up and validation batches.11. Responsible for shift activities in the FRD department as per schedule and instructions given by Manager.12. Ensuring equipment preventive maintenance is done as per schedule.13. Training of personnel on Job and department related activities.14. Reporting daily activities to Manager.

1. To carry out Formulation and Research activities as per department plan.2. Collection of literate related to the product from various site and to prepare summary report.3. Coordinating with the cross-functional departments such as Production, QA, QC, FAD for smooth running of the daily activities.4. Initiate stability testing of new products as per ICH guidelines.5. Executing the development of robust, stable and effective formulations and dosage form for new product development.6. Prepare specification, documentation, and reports related to product development.7. Prepare and review required FRD related documents activity like Master formula Record, Master Packing Record, PDR, logbooks and daily records.8. Prepare and review SOPs, and review appropriate documentation and test results for accuracy and completeness and compliance with SOPs/GMP requirement.9. Monitoring the qualification of department equipments and validation activities.10. To Prepare tech pack before execution of scale up and validation batches.11. Responsible for shift activities in the FRD department as per schedule and instructions given by Manager.12. Ensuring equipment preventive maintenance is done as per schedule.13. Training of personnel on Job and department related activities.14. Reporting daily activities to Manager.

1. To carry out Formulation and Research activities as per department plan.2. Collection of literate related to the product from various site and to prepare summary report.3. Coordinating with the cross-functional departments such as Production, QA, QC, FAD for smooth running of the daily activities.4. Initiate stability testing of new products as per ICH guidelines.5. Executing the development of robust, stable and effective formulations and dosage form for new product development.6. Prepare specification, documentation, and reports related to product development.7. Prepare and review required FRD related documents activity like Master formula Record, Master Packing Record, PDR, logbooks and daily records.8. Prepare and review SOPs, and review appropriate documentation and test results for accuracy and completeness and compliance with SOPs/GMP requirement.9. Monitoring the qualification of department equipments and validation activities.10. To Prepare tech pack before execution of scale up and validation batches.11. Responsible for shift activities in the FRD department as per schedule and instructions given by Manager.12. Ensuring equipment preventive maintenance is done as per schedule.13. Training of personnel on Job and department related activities.14. Reporting daily activities to Manager.

Monitor, evaluate, and improve manufacturing processes to enhance efficiency and yield.Identify and resolve process deviations, failures, and out-of-specification (OOS) issues.Implement Corrective and Preventive Actions (CAPA) for process improvements. Conduct process validation (PV), cleaning validation (CV), and continued process verification (CPV).Support equipment qualification (IQ/OQ/PQ) and ensure compliance with regulatory guidelines.Prepare validation master plans, protocols, and reports.Preferred candidate profile Perks and benefits

1) Budgeting/ Annual plan Budget preparation based on management direction o Total Revenue & Sales o Standard Material cost estimation Co-ordination with Costing team o Operational expenses budgeting from Plants and consolidation at company level Manpower cost: Co-ordination and finalization with HR team Utility consumption (Power, Coal, Water, etc.) Engineering and Maintenance budget (AMCs, services, R&M) Production consumables Safety & Effluent treatment expenses Quality control expenses Factory administration expenses Depreciation for assets Co-ordination with accounts Finance cost, Selling and distribution costs and corporate expenses o Gross Profit & Net Profit 2) Month Closing – MIS & Forecasting Ensure to right expenses booking in right GL and cost centres Tracking of all expenses as per budget and forecast Cost Variance analysis - Discuss with respective departments and finalize Quarterly forecasting Month end financial and CO books close in line with FI team Consolidation of P&L and reporting to management Prepare and present financial metrics in the BRM. Gross margin/contribution analysis 3) SAP ERP FI -CO Module Hands on experience in FI & CO modules (S4 HANA/ ECC) Understanding of accounting process in SAP Reports knowledge in SAP Others: Good knowledge and experience in Ms-Excel, PPT and any other reporting tools Good communication and presentation skill Work with cross-functional team, department HOD’

Role & responsibilities DMF, CTD, eCTD, ROW LOA, API & FP Declarations, Technical, Clinical & Non-clinical, BE studies, RMPs and PSURs Preferred candidate profile Perks and benefits

The Process Engineer is responsible for designing, optimizing, and troubleshooting chemical processes involved in API manufacturing. The role involves ensuring efficiency, compliance with regulatory standards, and process improvements to enhance productivity and safety. Process Development & Optimization:Design and develop API manufacturing processes to improve yield, efficiency, and quality.Conduct scale-up studies from lab to commercial production.Optimize process parameters to reduce cycle time and cost.Troubleshooting & Continuous Improvement:Identify and resolve process-related issues to maintain smooth production.Implement Six Sigma, Lean, or other continuous improvement methodologies.Perform root cause analysis (RCA) and corrective and preventive actions (CAPA).Technology Transfer & Validation:Assist in tech transfer from R&D to production.Develop and execute process validation protocols (IQ, OQ, PQ).Ensure compliance with GMP, FDA, and other regulatory guidelines Preferred candidate profile Perks and benefits

Role & responsibilities Candidates should have well versed knowledge on Costing, Budgeting, MIS and SAPPreferred candidate profile CMA qualified candidates only preferableImmediate joiners or within 30 days joiners more preferablePerks and benefits

Support the scale-up, production and technical transfer of pharmaceutical products.Support management of plant and process areas.Support installation, validation, maintenance and cleaning of equipment as required.Demonstrate the highest level of safety and consideration for working in the pilot plant Maintain clear and concise records of the pilot plant operationsWorking both independently and collaboratively to accomplish objectivesBuilding, operating, and maintaining laboratory and pilot scale equipmentWorking with various chemicals and hydrocarbonsHave basic knowledge of most of the processing equipment in the pilot plant in terms of set up, operation and clean up, and demonstrate expertise in at least one area to support the needs of the business unitsSupport product developers and scientist for all B/UEnsuring pilot plant is maintained to an appropriate standardAbility to execute designed experiments troubleshoot and make corrections during experimentationUtilize and demonstrate process knowledge and skills to make improvements in pilot plant performance and operating disciplineExcellent verbal and written communication, teamwork, collaboration, and organizational skills

1) Budgeting/ Annual plan Budget preparation based on management direction o Total Revenue & Sales o Standard Material cost estimation Co-ordination with Costing team o Operational expenses budgeting from Plants and consolidation at company level Manpower cost: Co-ordination and finalization with HR team Utility consumption (Power, Coal, Water, etc.) Engineering and Maintenance budget (AMCs, services, R&M) Production consumables Safety & Effluent treatment expenses Quality control expenses Factory administration expenses Depreciation for assets Co-ordination with accounts Finance cost, Selling and distribution costs and corporate expenses o Gross Profit & Net Profit 2) Month Closing – MIS & Forecasting Ensure to right expenses booking in right GL and cost centres Tracking of all expenses as per budget and forecast Cost Variance analysis - Discuss with respective departments and finalize Quarterly forecasting Month end financial and CO books close in line with FI team Consolidation of P&L and reporting to management Prepare and present financial metrics in the BRM. Gross margin/contribution analysis 3) SAP ERP FI -CO Module Hands on experience in FI & CO modules (S4 HANA/ ECC) Understanding of accounting process in SAP Reports knowledge in SAP Others: Good knowledge and experience in Ms-Excel, PPT and any other reporting tools Good communication and presentation skill Work with cross-functional team, department HOD’

1. To carry out Formulation and Research activities as per department plan.2. Collection of literate related to the product from various site and to prepare summary report.3. Coordinating with the cross-functional departments such as Production, QA, QC, FAD for smooth running of the daily activities.4. Initiate stability testing of new products as per ICH guidelines.5. Executing the development of robust, stable and effective formulations and dosage form for new product development.6. Prepare specification, documentation, and reports related to product development.7. Prepare and review required FRD related documents activity like Master formula Record, Master Packing Record, PDR, logbooks and daily records.8. Prepare and review SOPs, and review appropriate documentation and test results for accuracy and completeness and compliance with SOPs/GMP requirement.9. Monitoring the qualification of department equipments and validation activities.10. To Prepare tech pack before execution of scale up and validation batches.11. Responsible for shift activities in the FRD department as per schedule and instructions given by Manager.12. Ensuring equipment preventive maintenance is done as per schedule.13. Training of personnel on Job and department related activities.Preferred candidate profile Perks and benefits

Role & responsibilities Candidates should have well versed knowledge on Costing, Budgeting, MIS and SAPPreferred candidate profile CMA qualified candidates only preferableImmediate joiners or within 30 days joiners more preferablePerks and benefits

JD for Production (Pellets) Candidate must be having Pellets manufacturing experience for at least 6 8 years including Fluid bed processor and Conventional coating panCandidate must be having knowledge on Document preparation, reviewing(BMR BPR), and man power allocation for pellet manufacturingProper Review of technology transfer documents, customer documents and relevant API and Finished product monographs knowledge Cross functional team coordination with respect to QA, QC, marketing, R&D, RegulatoryProper knowledge and hands on experience on handling of Fluid bed processor, conventional coating pan, Granulation and drying, Extruder & Spheronizer, Proper knowledge for handing SAP, online in process entry, FP stock entry and other entries in SAP

The Process Engineer is responsible for designing, optimizing, and troubleshooting chemical processes involved in API manufacturing. The role involves ensuring efficiency, compliance with regulatory standards, and process improvements to enhance productivity and safety. Process Development & Optimization:Design and develop API manufacturing processes to improve yield, efficiency, and quality.Conduct scale-up studies from lab to commercial production.Optimize process parameters to reduce cycle time and cost.Troubleshooting & Continuous Improvement:Identify and resolve process-related issues to maintain smooth production.Implement Six Sigma, Lean, or other continuous improvement methodologies.Perform root cause analysis (RCA) and corrective and preventive actions (CAPA).Technology Transfer & Validation:Assist in tech transfer from R&D to production.Develop and execute process validation protocols (IQ, OQ, PQ).Ensure compliance with GMP, FDA, and other regulatory guidelines Preferred candidate profile Perks and benefits

1. To carry out Formulation and Research activities as per department plan.2. Collection of literate related to the product from various site and to prepare summary report.3. Coordinating with the cross-functional departments such as Production, QA, QC, FAD for smooth running of the daily activities.4. Initiate stability testing of new products as per ICH guidelines.5. Executing the development of robust, stable and effective formulations and dosage form for new product development.6. Prepare specification, documentation, and reports related to product development.7. Prepare and review required FRD related documents activity like Master formula Record, Master Packing Record, PDR, logbooks and daily records.8. Prepare and review SOPs, and review appropriate documentation and test results for accuracy and completeness and compliance with SOPs/GMP requirement.9. Monitoring the qualification of department equipments and validation activities.10. To Prepare tech pack before execution of scale up and validation batches.11. Responsible for shift activities in the FRD department as per schedule and instructions given by Manager.12. Ensuring equipment preventive maintenance is done as per schedule.13. Training of personnel on Job and department related activities.Preferred candidate profile Perks and benefits

Role & responsibilities Preferred candidate profile Perks and benefits

Role & responsibilities Tecnical Service DepartmentPreferred candidate profile B.Tech Chemical EngineerPerks and benefits

Role & responsibilities Candidates should have well versed knowledge on Costing, Budgeting, MIS and SAPPreferred candidate profile CMA qualified candidates only preferableImmediate joiners or within 30 days joiners more preferablePerks and benefits

Role & responsibilities AQAPreferred candidate profile M.ScPerks and benefits

Drug DiscoveryProcess DevelopmentFormulation ScienceAnalytical DevelopmentSynthetic Route OptimizationScale-Up ProcessTechnology TransferRegulatory Compliance (ICH, FDA, EMA, WHO-GMP)Good Laboratory Practices (GLP)Innovative MoleculesGreen Chemistry

Monitor, evaluate, and improve manufacturing processes to enhance efficiency and yield.Identify and resolve process deviations, failures, and out-of-specification (OOS) issues.Implement Corrective and Preventive Actions (CAPA) for process improvements. Conduct process validation (PV), cleaning validation (CV), and continued process verification (CPV).Support equipment qualification (IQ/OQ/PQ) and ensure compliance with regulatory guidelines.Prepare validation master plans, protocols, and reports.Preferred candidate profile Perks and benefits

The Process Engineer is responsible for designing, optimizing, and troubleshooting chemical processes involved in API manufacturing. The role involves ensuring efficiency, compliance with regulatory standards, and process improvements to enhance productivity and safety. Process Development & Optimization:Design and develop API manufacturing processes to improve yield, efficiency, and quality.Conduct scale-up studies from lab to commercial production.Optimize process parameters to reduce cycle time and cost.Troubleshooting & Continuous Improvement:Identify and resolve process-related issues to maintain smooth production.Implement Six Sigma, Lean, or other continuous improvement methodologies.Perform root cause analysis (RCA) and corrective and preventive actions (CAPA).Technology Transfer & Validation:Assist in tech transfer from R&D to production.Develop and execute process validation protocols (IQ, OQ, PQ).Ensure compliance with GMP, FDA, and other regulatory guidelines Preferred candidate profile Perks and benefits

Role & responsibilities AQAPreferred candidate profile M.ScPerks and benefits

Support the scale-up, production and technical transfer of pharmaceutical products.Support management of plant and process areas.Support installation, validation, maintenance and cleaning of equipment as required.Demonstrate the highest level of safety and consideration for working in the pilot plant Maintain clear and concise records of the pilot plant operationsWorking both independently and collaboratively to accomplish objectivesBuilding, operating, and maintaining laboratory and pilot scale equipmentWorking with various chemicals and hydrocarbonsHave basic knowledge of most of the processing equipment in the pilot plant in terms of set up, operation and clean up, and demonstrate expertise in at least one area to support the needs of the business unitsSupport product developers and scientist for all B/UEnsuring pilot plant is maintained to an appropriate standardAbility to execute designed experiments troubleshoot and make corrections during experimentationUtilize and demonstrate process knowledge and skills to make improvements in pilot plant performance and operating disciplineExcellent verbal and written communication, teamwork, collaboration, and organizational skills

Role & responsibilities DMF, CTD, eCTD, ROW LOA, API & FP Declarations, Technical, Clinical & Non-clinical, BE studies, RMPs and PSURs Preferred candidate profile Perks and benefits

Handling of HVAC system like scheduling HVAC filter cleaning, preventive maintenanceMonitoring of AMC schedules and periodical maintenance

Role & responsibilities Tecnical Service DepartmentPreferred candidate profile B.Tech Chemical EngineerPerks and benefits

Handling of HVAC system like scheduling HVAC filter cleaning, preventive maintenanceMonitoring of AMC schedules and periodical maintenance

Role & responsibilities Preferred candidate profile Perks and benefits

Role & responsibilities Preferred candidate profile Perks and benefits

Role & responsibilities Preferred candidate profile Perks and benefits

Role & responsibilities Preferred candidate profile Perks and benefits

Role & responsibilities DMF, CTD, eCTD, ROW LOA, API & FP Declarations, Technical, Clinical & Non-clinical, BE studies, RMPs and PSURs Preferred candidate profile Perks and benefits

Role & responsibilities Tecnical Service DepartmentPreferred candidate profile B.Tech Chemical EngineerPerks and benefits