23 Solvent Recovery Jobs

Job Title: Solvent Recovery System - SRS Location: Kakinada, AP Company: Lyfius Pharma About Lyfius Pharma is 100% subsidiary of Aurobindo Pharma. Its largest API Unit of Aurobindo. Lyfius spread across 236 acres in Kakinada SEZ and it is second largest API manufacturing facility in ASIA. Job Responsibilities: Overall operation & control of solvent recovery plant activity. Solvent recovery planning and execution based on plants production planning and running products recovered solvents generated, its recovery and recycling in same campaign and monitoring on (day to day basis.) Ensuring resources available (Equipment availability, utilities, BMR, raw material, manpower, safety items, etc.) Liaison with P.D.Lab, QC/QA/Store/Eng. Dept./EHS/Process Eng. for solving online troubleshooting. Implementation and monitoring of value addition systems like cGMP, House Keeping, Safety, EHS, and standard stem adherence. Product cost reduction by establishing recyclability after recovery of maximum product solvents by taking approval from P.D.Lab, QC, and R&D, R.A. & Q.A. and % recovery improvement, TRT reduction. Consistently monitoring and upgrading the improvement of solvent recovery and productivity, cost reduction, energy conservation, process implementation, efficiency, and services by efficient utilization of men material and machinery. And adapting innovative methodology and techniques for solvent recovery plant and purified water system facility up gradation. Preparation of daily reports by cross-checking and physically verifying Quality, Quantity, and yield and reporting to immediate superiors. Ensuring and monitoring the quality of distilled solvents, its timely close loop smooth and safe movements with systems to production blocks and always causes internal and external customer satisfaction. Ensure online all Documentation work, monthly reports, Quarterly reports, solvent recovery performance indicators, Training to subordinates and its record, data preparation, root cause analysis (process trend analysis). Preparation / Revision of BMR and SOPS and related other documents updating. Procurement of consumable items for solvent recovery plant and purified water systems. Ensuring and monitoring the quality of purified water and timely supply with close loop smooth and safe movements through systems to production blocks and updating online all Documentation related to the purified water plant, training to subordinates, and its record. Ensuring online all documents related to Change control, Incident, CAPA, URS, process qualification, and cleaning validation in both plants. Timely supply and fulfill the SPIL Internal units solvents requirement. And recycling maximum solvent which will bring down solvent CCS, and reduce in consumption of fresh solvents and inventory which helps to reduce product cost reduction. Operation of electronic systems like SAP HANA, Leave Portal (Metis), etc. Operation of Electronic systems like Track wise, Electronic Document Management Systems, etc.

Walk in Interview for the post of Production Supervisor/Executive @ Vadodara Location on 13th June 2025 Details are as follows:- Job Location: Jambusar, Gujarat Qualification: - B. Sc. / M. Sc. (Chemistry) / Diploma (Chemical) or B.E./B. Tech in Chemical Experience for Production: 5 to 9 years Experience for Supervisor & Executive role, Interview Date: 13th June 2025 ; Friday Interview Location: Baroda Productivity Council, Productivity House, 2nd Floor, BPC Road, Alkapuri, Vadodar E-mail- jmb.onboarding@piind.com Requirement for Production Candidates must have hands-on experience with DCS panel operation or filed operation in a DCS-operated plant Handling of multiple unit operations and processes simultaneously Knowledge of safety practices is a must. Experience in handling hazardous chemicals and solvents. Roles and Responsibilities:- 1. operational knowledge of YOKOGAVA DCS2. Production planning, control and executing batches, optimization in the plant.3. Supervising of batches charging and verification of RM quintets4. Monitoring and maintaining of the parameter as per SOP5. Handling Of solvent recovery process.6. Basic knowledge of process safety standards (MSDS) & general industry standards7. Distillation Column (Atmospheric & vacuum),8. Formulation of Final products for dispatch, packaging of the material, final products, at the warehouse.9. Operating of GLR and SS reactor, Centrifugal pump, piston pump, vacuum pump, Jet Ejector system.10. Safety Knowledge, Permit

Responsibility : 1. To ensure working in-line as per defined operational control and standard operation procedure. 2. To ensure effective housekeeping and safe work environment in surrounding area. 3. To awareness of EHS policy and EHS objective. 4. Establish, implement and maintain EHS management system pertaining to operation department. 5. To control and reduce wastages during performing operation activities. 6. To report unsafe conditions, unsafe act or near miss. 7. To Wear All PPE and refer MSDS before handling of material. 8. To First cheek Reactor. It should be clean & dry. MOISTURE FREE 9. To check out jacket of reactor it should be empty. 10. To check out side of reactor, it should be clean & dry. 11. To check wear & tear of gland of reactor, there should not be any particles. 12. TO check pipe used for charging. It should be clean & dry. 13. To check candle filter should be attached to charging line 14. All Liquid RAW materials to be charged through candle filter only 15. To check all line of reactor. All line should be closed. 16. To operate as per BMR instruction like 17. To Close all lines and apply water ring vacuumed in the reactor. 18. To Releasing of vacuum & starting of stirring of reactor. 19. To Purging of nitrogen as per BMR limit in kg in the reactor. 20. To applying slowly heating and temperature as per BMR instruction in the reactor. 21. To Applying of cooling /Chilling/Brine as per BMR instruction in the reactor. 22. To Release pressure from went line by jacket of reactor. 23. To Maintain rate of Distillation by slowly and increasing gradually in the reactor. 24. To Identify the EHS related corrective & preventive action. 25. Accountable for in process EHS of the product. 26. To stop working in unsafe area/ unsafe condition. 27. To report near-miss or accident observed. 28. Housekeeping in surrounding work area.

Lead the basic and detailed engineering of batch process plants involving key unit operations such as reaction, workup, filtration, drying, crystallization, distillation, and solvent recovery. Evaluate and map product integration into existing or new setups based on R&D data and pilot plant outcomes, ensuring scalability and process feasibility. Oversee the development of core engineering deliverables including: Block Flow Diagrams (BFD) Cycle time analysis Material and energy balances Equipment sizing Process Flow Diagrams (PFD) and Piping & Instrumentation Diagrams (P&ID) HAZOP studies and risk assessments Direct the preparation of plant layouts , including equipment layout, plan, and elevation drawings, ensuring optimal space utilization and compliance with safety standards. Review and approve process and utility data sheets and lead technical bid evaluations for critical equipment and systems. Provide technical leadership in troubleshooting operational issues in existing plants, driving root cause analysis and sustainable solutions. Contribute to project cost estimation by providing accurate process inputs and equipment specifications. Lead pre-commissioning and commissioning activities , ensuring smooth handover from design to operations. Ensure design compliance with cGMP and USFDA standards , integrating regulatory requirements into engineering practices The Person Qualifications & Experience B.E./B.Tech in Chemical Engineering from premier institutes (IIT/NIT) with 12 15 years of experience in batch process plants. Strong communication, analytical, and critical thinking skills. High attention to detail with sound general and functional knowledge. Proficient in applying engineering concepts in day-to-day operations; recognized as a subject matter expert. Personal Attributes Excellent interpersonal and people management skills. Strategic thinker with a solution-oriented mindset and strong execution capabilities. Effective in matrix organizations; adept at cross-functional collaboration. Proven leadership in building and retaining high-performing teams

Company Information Company Name: Global Calcium Pvt Ltd Location: Hosur Responsibilities Key Responsibilities: Operate and monitor solvent recovery systems including distillation columns, condensers, receivers, and associated utilities. Perform batch-wise solvent recovery, monitor parameters (temperature, pressure, flow rate), and make necessary adjustments to ensure optimal performance. Ensure compliance with GMP, SOPs, and safety protocols in all SRP operations. Coordinate with QA/QC for sampling and approval of recovered solvents. Maintain accurate records of solvent recovery, utility consumption, downtime, and yield reports. Support maintenance activities, troubleshoot minor issues, and escalate technical problems to the engineering team. Adhere to statutory environmental norms (CPCB/SPCB guidelines) for air and water discharge. Qualifications B.Tech in Chemical Engineering, Chemistry, or relevant field. 2-4 years of experience in Solvent Recovery in the pharmaceutical industry.

Producing Intermediates/API/Solvent Recovery according to pre-approved instructions and to record the same in respective BPR/documents. To perform the cleaning activity as per the procedure and to record the same in respective BCR/documents. Maintaining the Intermediate/Pharma/SRP and equipment clean and well appropriately disinfected. To ensure that the respective equipment is calibrated Maintaining the respective equipment /Area in clean condition. Online updating of equipment status boards w.r.t to equipment status. Identifying /Labelling of accessories (e.g. Scoop /Scrapper/Hose pipe/Filter bags/ AHU filters / micron filter cartridges) and storing the same in designated place. Identify the abnormalities associated risk and objectives by cross verifying the interlocks in equipment. To ensure the availability of utilities and to maintain the same by requesting utility department whenever required. Material Handling: Receiving the raw material from the stores and storage of raw materials in the designated place Identification and storage of intermediates/ API s in the designated place. Maintaining the RM/ intermediate/ rejected material storage area clean and when appropriate disinfected. To maintain the accessories per respective SOP. Documentation:

1) To be follow monthly production dispatch planning, indent packaging materials to meet the production targets. 2) To be handle in-process control packaging activities in the production department as per defined specification. 3) To ensure that the plant equipment used for processing are utilised with their Optimum capacity. 4) To analyse batch to batch for Corrective & Implement the same. To be member of investigation of market complain as and when received from the customer. 5) To help the Supervisors to reduce the time cycles of batch packing in existing and developmental products. 6) To help the dispatch department to get the maximum output of final packing as per customer PO. 7) To help the Supervisors (Shift in Charge) in the improvisation of material management in terms of Handling, Consumption, Accounting and Disposal if any. 8) To analyse monthly output of each workstation for DOWNTIMES & Consciously reduce it. 9) To generate monthly Production Reports as stipulate by Management. 10) To be ensure dispatching product to the customer as per their requirements and fill related check list. 11) To Ensure Housekeeping standards within the packaging Area. 12) To be record packaging BPCR of relevant products in time and train down line staff accordingly. 13) Continuously suggest ways &means to achieve requirements of customer, goods delivery in time and zero complaint. 14) To impart training to down the line employees & keep them updated with latest related developments as per existing SOPs. 15) To be prepare and review QMS activities like SOPs, related format etc. 16) To get involved in Equipment Qualifications, Change Control, Handling of deviation, Handling of CAPA, Internal audit, Process validation, Market complaint, APQR, Returned goods, Investigations, Calibrations, Data integrity.

1. Minimizing Plant break down hours. 2. Increased Fly Ash absorption. Scheduled clinker, Gypsum or flyash analysis. Grinding aid quality to be checked every week. 3. Achieve cement production of 2.4 MTPA maintaining quality. To increase TPH. Through process optimization. 4. Regulating process parameter, flow etc and taking corrective action. 5. Specific power consumption of PPC. 6. Thorough Process Optimization. 7. Corrective action to be taken after reviewing circuit sample results. 8. Complying safety norms. 9. Operation Maintenance of QC Lab activities. Qualifications: Diploma Minimum Experience Level: 4-6 Years Report to: Assistant General Manager

Producing Intermediates/API/Solvent Recovery according to pre-approved instructions and to record the same in respective BPR/documents. To perform the cleaning activity as per the procedure and to record the same in respective BCR/documents. Maintaining the Intermediate/Pharma/SRP and equipment clean and well appropriately disinfected. To ensure that the respective equipment is calibrated Maintaining the respective equipment /Area in clean condition. Online updating of equipment status boards w.r.t to equipment status. Identifying /Labelling of accessories (e.g. Scoop /Scrapper/Hose pipe/Filter bags/ AHU filters / micron filter cartridges) and storing the same in designated place. Identify the abnormalities associated risk and objectives by cross verifying the interlocks in equipment. To ensure the availability of utilities and to maintain the same by requesting utility department whenever required. Material Handling: Receiving the raw material from the stores and storage of raw materials in the designated place Identification and storage of intermediates/ API s in the designated place. Maintaining the RM/ intermediate/ rejected material storage area clean and when appropriate disinfected. To maintain the accessories per respective SOP. Documentation:

Walk in Interview for the post of Production Supervisor/Executive @ Vadodara Location on 04th April 2025 Details are as follows:- Job Location: Jambusar, Gujarat Qualification: - B. Sc. / M. Sc. (Chemistry) / Diploma (Chemical) or B.E./B. Tech in Chemical Experience for Production: 3 to 6 years Experience for Supervisor role, 4 to 8 years for Executive role Interview Date: 04th April 2025 ; Friday Interview Location: Baroda Productivity Council , Productivity House, 2nd Floor, BPC Rd, Alkapuri, Vadodara E-mail- jmb.onboarding@piind.com Requirement for Production Candidates must have hands-on experience with DCS panel operation or filed operation in a DCS-operated plant Handling of multiple unit operations and processes simultaneously Knowledge of safety practices is a must. Experience in handling hazardous chemicals and solvents. Roles and Responsibilities:- 1. operational knowledge of YOKOGAVA DCS2. Production planning, control and executing batches, optimization in the plant.3. Supervising of batches charging and verification of RM quintets4. Monitoring and maintaining of the parameter as per SOP5. Handling Of solvent recovery process.6. Basic knowledge of process safety standards (MSDS) & general industry standards7. Distillation Column (Atmospheric & vacuum),8. Formulation of Final products for dispatch, packaging of the material, final products, at the warehouse.9. Operating of GLR and SS reactor, Centrifugal pump, piston pump, vacuum pump, Jet Ejector system.10. Safety Knowledge, Permit

Role & responsibilities 1)Handling of Equipment's and troubleshooting in production department as per SOP. 2)Provide training to operators regarding batch parameters and safety measures regarding hazardous chemicals and process. 3)Communicate any maintenance to engineering department during batch manufacturing process. 4)Communicate any deviation to Quality Assurance department during batch manufacturing process. 5)Performing the production activities through DCS 6)Receipt, check and issuance of Row material from WH.

We have opening of two positions of Production Engineers (Male only) at our company Shuddhi industries. Education: BE/Diploma Chemical Engg Work Ex : 0 -10 year of experience Benefits : PF & ESI after 6 months. Job Profile : Batch monitoring & Processing as Per Production Plan. Handling shift manpower e.g Operator, Helper. Fill BMR & Other documents as per ISO norms. Co-ordinate with maintenance department, QC department. Raw Material managament.

Job Title: Solvent Recovery SRS Manager / Dy. Manager Location: Kakinada, AP Company: Lyfius Pharma About Lyfius Pharma is 100% subsidiary of Aurobindo Pharma. Its largest API Unit of Aurobindo. Lyfius spread across 236 acres in Kakinada SEZ and it is second largest API manufacturing facility in ASIA. Job Responsibilities: Overall operation & control of solvent recovery plant activity. Solvent recovery planning and execution based on plants production planning and running products recovered solvents generated, its recovery and recycling in same campaign and monitoring on (day to day basis.) Ensuring resources available (Equipment availability, utilities, BMR, raw material, manpower, safety items, etc.) Liaison with P.D.Lab, QC/QA/Store/Eng. Dept./EHS/Process Eng. for solving online troubleshooting. Implementation and monitoring of value addition systems like cGMP, House Keeping, Safety, EHS, and standard stem adherence. Product cost reduction by establishing recyclability after recovery of maximum product solvents by taking approval from P.D.Lab, QC, and R&D, R.A. & Q.A. and % recovery improvement, TRT reduction. Consistently monitoring and upgrading the improvement of solvent recovery and productivity, cost reduction, energy conservation, process implementation, efficiency, and services by efficient utilization of men material and machinery. And adapting innovative methodology and techniques for solvent recovery plant and purified water system facility up gradation. Preparation of daily reports by cross-checking and physically verifying Quality, Quantity, and yield and reporting to immediate superiors. Ensuring and monitoring the quality of distilled solvents, its timely close loop smooth and safe movements with systems to production blocks and always causes internal and external customer satisfaction. Ensure online all Documentation work, monthly reports, Quarterly reports, solvent recovery performance indicators, Training to subordinates and its record, data preparation, root cause analysis (process trend analysis). Preparation / Revision of BMR and SOPS and related other documents updating. Procurement of consumable items for solvent recovery plant and purified water systems. Ensuring and monitoring the quality of purified water and timely supply with close loop smooth and safe movements through systems to production blocks and updating online all Documentation related to the purified water plant, training to subordinates, and its record. Ensuring online all documents related to Change control, Incident, CAPA, URS, process qualification, and cleaning validation in both plants. Timely supply and fulfill the SPIL Internal units solvents requirement. And recycling maximum solvent which will bring down solvent CCS, and reduce in consumption of fresh solvents and inventory which helps to reduce product cost reduction. Operation of electronic systems like SAP HANA, Leave Portal (Metis), etc. Operation of Electronic systems like Track wise, Electronic Document Management Systems, etc.

JD: 1. Candidate must have knowledge of plant Equipment- Reactor, ANF, ANFD, Centrifuge ETC 2. Candidate must have knowledge of Solvents. 3. Candidate must have knowledge of chemical reaction. 4. Candidate must have knowledge of Safety.

Key Responsibilities. Intermediate/Clean room/SRP: Producing Intermediates/API/Solvent Recovery according to pre-approved instructions and to record the same in respective BPR/documents. To perform the cleaning activity as per the procedure and to record the same in respective BCR/documents. Maintaining the Intermediate/Pharma/SRP and equipment clean and well appropriately disinfected. To ensure that the respective equipment is calibrated Maintaining the respective equipment /Area in clean condition. Online updating of equipment status boards w.r.t to equipment status. Identifying /Labelling of accessories (e.g. Scoop /Scrapper/Hose pipe/Filter bags/ AHU filters / micron filter cartridges) and storing the same in designated place. Identify the abnormalities associated risk and objectives by cross verifying the interlocks in equipment. To ensure the availability of utilities and to maintain the same by requesting utility department whenever required. Material Handling: Receiving the raw material from the stores and storage of raw materials in the designated place Identification and storage of intermediates/ API s in the designated place. Maintaining the RM/ intermediate/ rejected material storage area clean and when appropriate disinfected. To maintain the accessories per respective SOP. Documentation: To indent, receive and issue therequired documents with in timeline according to pre-approved instructions. To ensure that documents being recorded contemporaneously. To ensure the records are updating contemporaneously and to facilitate the required documents. To ensure the availability of calibration documents where ever required. To ensure that those documents are completed and signed. To ensure the online entries of status board, log books and daily updating documents. To ensure the accessories are properly maintained/ destructed as per the respective SOP and it is properly documented. To submit the completed documents with in the timeline as per respective SOP Safety, health and environment: On line monitoring of the environment conditions in process area Person Profile . Qualification - Degree in Science / Graduate Engineers - Chemical/Diploma in Chemical Engineering (Chemistry / Chemical / PCM / Bio-Chemistry) Experience- 3 to 5 Years of relevant experience from API industry only

Key Responsibilities. Intermediate/Clean room/SRP: Producing Intermediates/API/Solvent Recovery according to pre-approved instructions and to record the same in respective BPR/documents. To perform the cleaning activity as per the procedure and to record the same in respective BCR/documents. Maintaining the Intermediate/Pharma/SRP and equipment clean and well appropriately disinfected. To ensure that the respective equipment is calibrated Maintaining the respective equipment /Area in clean condition. Online updating of equipment status boards w.r.t to equipment status. Identifying /Labelling of accessories (e.g. Scoop /Scrapper/Hose pipe/Filter bags/ AHU filters / micron filter cartridges) and storing the same in designated place. Identify the abnormalities associated risk and objectives by cross verifying the interlocks in equipment. To ensure the availability of utilities and to maintain the same by requesting utility department whenever required. Material Handling: Receiving the raw material from the stores and storage of raw materials in the designated place Identification and storage of intermediates/ API s in the designated place. Maintaining the RM/ intermediate/ rejected material storage area clean and when appropriate disinfected. To maintain the accessories per respective SOP. Documentation: To indent, receive and issue therequired documents with in timeline according to pre-approved instructions. To ensure that documents being recorded contemporaneously. To ensure the records are updating contemporaneously and to facilitate the required documents. To ensure the availability of calibration documents where ever required. To ensure that those documents are completed and signed. To ensure the online entries of status board, log books and daily updating documents. To ensure the accessories are properly maintained/ destructed as per the respective SOP and it is properly documented. To submit the completed documents with in the timeline as per respective SOP Safety, health and environment: On line monitoring of the environment conditions in process area Person Profile . Qualification - Degree in Science / Graduate Engineers - Chemical/Diploma in Chemical Engineering (Chemistry / Chemical / PCM / Bio-Chemistry) Experience- 5-10 Years of relevant experience from API industry only

Greetings for the day! Aarti Pharmalabs Ltd is looking for To provide technical support for process optimization, batch cycle time reduction, product yield improvement, capacity constraint analysis, solvent recovery and energy saving initiatives for cost reduction. To sustain business profitability by monitoring & optimizing the cost of production & minimizing the losses. Focus on capacity enhancement, improvement of existing processes, batch-cycle time reduction and solvent recovery. Expertise in basic & detailed engineering activities like energy & mass balance, PFD, P&ID, equipment sizing, utility requirement, P&ID review, techno-commercial evaluation and project management. Introduction of new technologies in consonance with latest best manufacturing practices in the industry. Knowledge of calculation Heat and Mass balance and Utility requirement for a process.Mapping of the product, selection of equipment and facility creation.Compilation of experimental observations and analytical results for tech transfer reportSuccessful execution and validation of new processes by closely working with R&D/Production and other cross functional teams by following good manufacturing and engineering practices. Effective planning and timely execution of process engineering initiatives as also trial & validation of batches for existing products in coordination with R&D/Production/QA/QC/EHS etc. Conceiving various improvement schemes, process feasibility studies, as also developing techno- commercial proposals.

Role & responsibilities : Manpower Planning, Chemical Handling, Chemical Production, Shift Planning etc.

Location : Ankleshwar, Gujraat Experience : 2-5 years Shift : Rotational Shift Incharge - Metal Solvent Extraction Plant (Hydrometallurgy) Shift Operations Management : Ensure smooth and efficient running of the metal solvent extraction process during assigned shifts, adhering to operational standards and production targets. Team Supervision : Manage and coordinate shift workers, providing guidance and support to ensure safety, productivity, and compliance with operational protocols. Process Optimization : Monitor key performance indicators (KPIs) and take proactive measures to optimize solvent extraction processes and minimize downtime. Health, Safety, and Environmental Compliance : Ensure strict adherence to safety standards, environmental regulations, and operational guidelines to minimize risks. Troubleshooting & Problem-Solving : Quickly identify and resolve operational issues during the shift, ensuring minimal disruption to the process. Reporting & Documentation : Maintain accurate records of shift activities, production data, and any incidents or anomalies for management review. Equipment Maintenance Coordination : Coordinate with maintenance teams to ensure timely inspection and upkeep of machinery and equipment to avoid unplanned breakdowns. Continuous Improvement : Proactively suggest and implement improvements to enhance process efficiency, reduce costs, and increase overall plant productivity.

Job Role : Sr.Manager - Process Engineering Job Function : Global Process & Technology Location : Baroda Job Summary : GP&T Lead worked with site GP&T leads to support all operations related technical requirements. Support for failure investigations and its reduction, Process improvement with respect to robustness Areas of Responsibility : Co-ordinate with all Site GP&T team for GP&T functions. Work plan preparation and tracking for GP&T activities. Provide technical support for the investigations of OOS, OOT, Trouble shooting and unplanned deviation of all API manufacturing sites for root cause identification. Co-Ordinate with AD/R&D for impurity identification. Should have knowledge of technique of Characterization. Coordinate with RA for technical requirement for additional filing/ Query response. Coordinate with site quality team for regulatory audit preparation and to provide technical support during Audit. Participate for PSD/BD and TD related failure with R&D and process Eng. Work on process robustness and reduction of repeated failure Support for reprocess method development for inventory liquidation. Update and maintain GP&T tracker. Budget preparation and maintaining. Provide technical support for LCM technology transfer Co-ordinate & Monitor with site GP&T team for Vendor qualification, Inventory reduction, Control of yield loss, EHS related activities, Solvent recovery etc Educational Qualification : PhD in Organic Chemistry Experience : 15+ year

" Introduction: Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S. Bhartia and Mr. Hari S. Bhartia with strong presence in diverse sectors like Pharmaceuticals, Life Science Ingredients, Contract Research & Development Services, Therapeutics, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Group has global presence employing around 42,000 people across the globe with over 2,400 in North America. Jubilant Pharmova Limited Jubilant Pharmova Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radiopharma, Allergy Immunotherapy, CDMO Sterile Injectables, Contract Research Development and Manufacturing Organisation (CRDMO), Generics and Proprietary Novel Drugs businesses. In the Radiopharma business, the Company is involved in manufacturing and supply of Radiopharmaceuticals with a network of 46 radio-pharmacies in the US. The Company s Allergy Immunotherapy business is involved in the manufacturing and supply of allergic extracts and venom products in the US and in some other markets such as Canada, Europe and Australia. Jubilant through its CDMO Sterile Injectables business offers manufacturing services including sterile fill and finish injectables (both liquid and lyophilization), full-service ophthalmic offer (liquids, ointments & creams) and ampoules. The CRDMO business of the Company includes the Drug Discovery Services business that provides contract research and development services through two world-class research centres in Bangalore and Noida in India and the CDMO-API business that is involved in the manufacturing of Active Pharmaceutical Ingredients. Jubilant Therapeutics is involved in Proprietary Novel Drugs business and is an innovative biopharmaceutical company developing breakthrough therapies in the area of oncology and autoimmune disorders. The company operates six manufacturing facilities that cater to all the regulated market including USA, Europe and other geographies. Find out more about us at www.jubilantpharmova.com . The Position Organization- Jubilant Pharmova Limited Designation Chemist Production Location- Nanjangud, Mysore Key Responsibilities. Intermediate/Clean room/SRP: Producing Intermediates/API/Solvent Recovery according to pre-approved instructions and to record the same in respective BPR/documents. To perform the cleaning activity as per the procedure and to record the same in respective BCR/documents. Maintaining the Intermediate/Pharma/SRP and equipment clean and well appropriately disinfected. To ensure that the respective equipment is calibrated Maintaining the respective equipment /Area in clean condition. Online updating of equipment status boards w.r.t to equipment status. Identifying /Labelling of accessories (e.g. Scoop /Scrapper/Hose pipe/Filter bags/ AHU filters / micron filter cartridges) and storing the same in designated place. Identify the abnormalities associated risk and objectives by cross verifying the interlocks in equipment. To ensure the availability of utilities and to maintain the same by requesting utility department whenever required. Material Handling: Receiving the raw material from the stores and storage of raw materials in the designated place Identification and storage of intermediates/ API s in the designated place. Maintaining the RM/ intermediate/ rejected material storage area clean and when appropriate disinfected. To maintain the accessories per respective SOP. Documentation:

5 years & above in API. Exp. in GMP & Safety in handling production equipment Operate the various equipment under supervision Knowledge of DCS & ERP Exp. of Hydrogenation Exp. of Distillation Column share your cv on jobs@nglfinechem.com Required Candidate profile should have Experience in Hydrogenation or in Distillation Column

The Position will be responsible for providing basic data to HOD for smooth functioning of process development activity for new molecules for fine-chemical business. This would include observing demo at R&D, scale up studies, preparing basic engg package, and conducting trials at commercial scale & hand over to operations. To deliver their rated capacity, quality & Input / Output norms. Strategic Responsibilities Basic work for document transfer schedule for new projects being commercialised to meet the timeline. Participation in the meetings & provide inputs as & when required by Dept. head. Operational Responsibilities Preparation of BFD for commercial scale. Preparation of PFD. RM norms calculation. Calculation of Utility estimation. Conducting trials for Solvent recovery methods as per HOD s instruction. Basic work for Off gas handling scheme. Provide backup calculation & data for process safety. Preliminary equipment selection & sizing. Generating data for MOC studies in pilot plant /KL. Preparing SOP for commercial scale. Preparing Objectives for scale up trials, its observations, recommendations & conclusion. Identification of critical parameters & its suggestions/implementation in the plant SOP. Calculation for Time cycle. Writing control logic of process required for DCS. Financial Responsibilities Provide data for BOM to HOD for commercial scale. Contribute to budget proposals Contribute to budgetary controls within the area of responsibility. People Responsibilities To attend training programs for process engineers in PD. Provide process training (3 stages) to operation team before startup of new project. Coordination with kilo/ plant/ R&D, QC for day to day activity. Ensure smooth working of the department to maintain high morale of the workforce Continuously improve processes to ensure quality and efficiency Participate in selection of highly qualified process development team. Set goals and review performance. Identify development needs. Education Qualification Chemical/B. Tech Chemical/M. Tech Work Experience 3-5 year experience Industry to be Hired from Chemical based industry Functional Competencies Preparation of BFD/PFD, Mass balance, Utility calculations Conducting trials in the kilo/pilot plant. Demonstration of batches at commercial scale