Jubilant Bhartia Group 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, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R and D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services-from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)-in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide. In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology, in-vivo , in-vitro models and translational sciences. Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions. Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology and In-vitro ADME Medicinal Chemistry Synthetic and Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the world's leading pharmaceutical, biotech companies, academic institutions and research foundations. Find out more about us at www.jubilantbiosys.com ;;;;; ; The Position Organization; : - Jubilant Biosys Designation and Level: - SRA Location: - Greater Noida Department: - Analytical Key Responsibilities Having exposure of 1-8y in analytical chemistry (SFC or purification) Interaction with synthetic team and problem solving skills. Should be able to handle the respective instrument Knowledge of instrumental technique with its application Should be able to handle routine analysis independently on respective instrument . SFC: Support analytical chiral method development, chiral purification in SFC/Normal Phase. Maintain TAT as per target. Periodic maintenance, calibration of SFC instruments, completing documentation on time, performing additional analysis (chiral screening) when required. Candidate requirements: . ;;;; Educational qualification: Post Graduate Degree in Chemical/Life Sciences - M. Pharm, M. Sc., . ;;;; Technical Knowledge: ; Person Profile Qualification: - M. Sc (Analytical Chemistry) Experience: - 2 years of relevant experience Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances.
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 and 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 Radio pharma, Allergy Immunotherapy, CDMO Sterile Injectable, Contract Research Development and Manufacturing Organisation (CRDMO), Generics and Proprietary Novel Drugs businesses. In the Radio pharma 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 Injectable business offers manufacturing services including sterile fill and finish injectable (both liquid and lyophilisation), full-service ophthalmic offer (liquids, ointments and 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 Biosys Limited Designation ;: Senior Manager / Associate Director - Finance and Accounting Location;;; : Bangalore Responsible for following activities: Financial Planning and Analysis (FP and A): Lead the annual budgeting, forecasting, and long-range planning processes. Provide strategic insights and recommendations to senior leadership based on financial analysis. Monitor key performance indicators (KPIs) and variance analysis to support decision-making. Analytical Dashboards and Reporting: Design and implement interactive dashboards using tools like Power BI, Tableau, or similar. Automate reporting processes to improve efficiency and accuracy. Present financial data in a clear, actionable format for cross-functional stakeholders. Consolidation of Accounts: Oversee monthly, quarterly, and annual financial close processes. Ensure timely and accurate consolidation of financial statements across entities. Maintain compliance with accounting standards (IFRS/GAAP) and internal controls. Business Finance Partnering: Collaborate with business units to evaluate financial impact of strategic initiatives. Support pricing strategies, cost optimization, and investment decisions. Act as a trusted advisor to operational teams, driving financial accountability. Qualifications and Skills: CA / CPA or MBA from top premium colleges 15+ years of progressive experience in finance and accounting roles. Strong expertise in FP and A, financial consolidation, and business finance. Proficiency in financial modeling, Excel, and dash boarding tools. Excellent communication, leadership, and stakeholder management skills. Experience in a multinational or matrixed organization is preferred. Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, Please visit our LinkedIn Page- https://www.linkedin.com/company/jubilantpharmova/mycompany/
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 and 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 and 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 - Associate Director - Computer System Validation Location- Nanjangud, Mysore Responsible to harmonize, ensure and standardize policies and procedures for computerized system validations and ensure effective implementation of the computerized system validation in coordination with corporate quality and with all departments of the plant with respect to Computer System Validation (CSV). Responsible to assist site personnel/management in developing protocols, test cases, validation packages, etc. for validations of computerized system. Responsible to evaluate validation requirement for computerized systems used for GxP purposes in various department of the plant. Provide guidance on the interpretation of regulatory requirement and guidelines for GxP Computerized systems from regulatory agencies and organizations in relative to CSV/ IT Compliance activities. Responsible to review of CSV requirements in the validation protocols by defining the required test cases of IQ/OQ for computerized system of equipment's and instruments etc., and also tracking of CSV implementation. Ensure the compliance-related issues handled independently aligned with the processes and controls on computerized systems. Responsible to identify, communicate and manage compliance risks, breaches and issues, and monitor corrective action to mitigate the risk through risk assessment related to computerized systems. Responsible to independently assess the regulatory compliance activities of computerized system e.g. GxP, FDA, Annex 11 etc. To conduct internal reviews and compliance at site on GxP Computerized systems. To assess and improve the cGMP practices and procedures on computerized system validations. Responsible for data governance and management controls in reviewing complete, consistent, accurate, truthful and reliable data in all GxP Computerized systems required as per regulatory requirements. Ensure all incidents related computerized systems are logged, tracked, monitored and closed after it has been detected. Review and approval of equipment qualification and re-qualification documents and monitoring of equipment, utility and facility qualification activities. Review and approval of equipment layouts and Piping and Instrument Diagrams (P and IDs). Review and approval of Qualification Summary Report for the equipment. Review of the engineering documents associated with SOP's. Review of VMP schedules of qualification. Responsible for review and guiding Quality Risk Managements related to Computerized Systems, Equipment qualification, Utility qualification and facility qualification. Responsible for review, monitoring and guiding Quality Management system such are Change controls, events/deviations and CAPAs in Track wise related to CSV, Equipment qualification, Utility qualification and facility qualification. Ensure all CAPAs related to Computerized system, Equipment qualification, Utility qualification and facility qualification are closed as per the CAPA specified time lines. Coordination and implementation of CAPA for all internal / external audit observations related to CSV, Equipment qualification, Utility qualification and facility qualification. Person Profile. Education Qualification: B.Tech / M.Tech / M.Sc - Chemical Engineering / Organic Chemistry Experience Range : 18+ years Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, Please visit our LinkedIn Page- https://www.linkedin.com/company/jubilantpharmova/mycompany/
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 and 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 and 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 Biosys Limited Designation - Deputy Manager - Technical Services (TSD) Location- Nanjangud, Mysore Shall be responsible for the following activities: Successful Scale-up for new molecule from Lab to pilot scale and commercial scale. Basic engineering for new product commercialisation or capacity enhancement projects or environment management system. Review of basic engineering package for capacity enhancement which includes capacity calculation, Process block diagram, Equipment sizing, Utility calculation etc. Capex estimation. Coordinating with Vendors/Consultants for various deliverables at different stages of the Project. Review and approve of P and IDs, Lay out, technical specification, Vendor / Consultant documents for the projects. Review and approve of Qualification documents such as URS, Design Specification, FRS, DQ, IQ and OQ. Commissioning support and product deliverables. De-bottlenecking of existing capacity and proposal for Capacity enhancement. Collaborating Cross functional team for new process validation and commercialization. Identification and implementation of new technologies for various unit operations. Performance evaluation of the systems and supporting various cost effective, energy conserving process engineering activities of the department.;;; Supporting R and D for technology development. Guide the team for resolution and smooth execution. Identification of improvements in existing process followed by implementation in pilot plant and commercial plant with collaboration with R and D. Review of the equipment's mapped for New Products and Plan for the Modifications/Resources in coordination with manufacturing team. Review and Approve the process outlines and plan for the scale up and validations Review and Approve of Equipment equivalence reports, Scale-up reports, Validation Protocol, Validation reports, Cost reports and other Pilot Plant and Technology transfer related documents. Trouble shooting and investigation of Scale-up related Problems, Routine commercial OOS/OOT's by identifying root causes and suggesting Corrective and Preventive action to avoid failure, deviations and change controls through Track wise system. Coordinate during internal and external audits and ensuring compliance with respect to Quality system. Submission of relevant data for DMF filing. Driving Task force activities/ Key continuous improvement initiatives with respect to yield improvement, solvent recovery. Prepare and review CRDMO costing with necessary inputs as per project management / customer requirement. Person Profile. Education Qualification: B.Tech / M.Tech Chemical Engineering Experience Range : 12+ years Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, Please visit our LinkedIn Page- https://www.linkedin.com/company/jubilantpharmova/mycompany/
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 and 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 Biosys Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radio pharma, Allergy Immunotherapy, CDMO Sterile Injectable, Contract Research Development and Manufacturing Organisation (CRDMO), Generics and Proprietary Novel Drugs businesses. In the Radio pharma 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 Injectable business offers manufacturing services including sterile fill and finish injectable (both liquid and lyophilisation), full-service ophthalmic offer (liquids, ointments and 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 Biosys Limited Designation - Deputy Manager - Utility Location- Nanjangud, Mysore Job Summary - Key Responsibilities. Overall Incharge of HVAC and Utility Systems (Operation and Maintenance) Facing Audits, working on Audit Compliance. Trouble Shooting. Maintenance of HVAC and Utility Installations (Preventive, Corrective and Breakdown Maintenance), Management for all HVAC and Utility related systems like AHU, Chiller, Boiler, Chilled Water, Chilled Brine, Hot Water, Cooling Water, Air, Nitrogen, DM Plant, Purified Water Plant etc. Ensuring uninterrupted supply of HVAC related Utilities Ensuring Uninterrupted supply of Utilities. Planning of spares for Critical / Non critical equipment and initiate procurement action. To inspect the spares received and approve GRN. To monitor HVAC Systems operations and to propose and implement Energy conservation initiatives SOP and On job training to subordinates. To Prepare, review, update and maintain documents like PM Checklist, Schedules, Formats, SOP's and Qualifications related to Utility and HVAC equipment's. Tracking of pending notifications and work allotment for Asst. Foreman, Technician and Contractors Working with SAP-ERP system like handling Service requests, Work orders, Purchase requests, PM, Service entry, Reservations to withdraw materials, RGP/NRGP and GRN approvals etc. Verify the quality and quantity of work carried out by Contractors and Certification of contractor invoices. Revenue, Capex Budget preparation, monitoring on monthly basis and Control within the approved budget. Compliance Wire coordinator for Engineering Department. Vendor evaluation and qualifications. Equipment inspection and testing at vendor site. Handling deviations, Change management and review through track wise. Handling of EDMS software for Qualification Protocols, SOP's, Schedules etc. Implementation of Six Sigma activities, PMA, Energy Conservation and project works. To maintain the AHU and #39;s of all the plant areas and clean rooms. To support HVAC Validation activity. To coordinate with service providers to get the job done. Audit compliance and documentation relevant to ISO, cGMP, Customer and Regulatory audits. Ensure safety compliance for self and reporting team. Upgrade the HVAC / AHU system to current engineering standard and compliance level. To monitor Utility Equipment Efficiency (OPE and OEE) and to propose and implement Energy conservation initiative. Monitoring of Utility consumptions, efficiency and preparing cost of utilities. Review and approve of Utility documents Person Profile . Qualification - BE / B.Tech - Mechanical Experience- 10+Years Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, Please visit our LinkedIn Page- https://www.linkedin.com/company/jubilantpharmova/mycompany/
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 and 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 Biosys 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 and 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 Biosys Limited Designation - Associate Director - Quality Control Location- Nanjangud, Mysore Job Summary - Key Responsibilities. Compliance and Documentation Ensure lab compliance with established procedures and regulatory standards. Review QC-related documents: SOPs, specifications, methods of analysis, method transfer documents. Ensure 21 CFR Part 11 compliance for analytical instruments (Ref: 21 CFR 211 Subpart I). 2. Analytical Activities Oversee stability studies and holding time studies. Release analytical reports for raw materials, packing materials, intermediates, APIs, and in-process samples. Provide analytical support and technical clarifications to customers. 3. Investigations and CAPA Lead investigations into OOT, OOS, incidents, and deviations. Ensure timely closure and robust implementation of CAPAs to prevent recurrence. 4. Equipment and Infrastructure Ensure preventive maintenance and calibration of instruments. Participate in technical discussions for new equipment procurement. Approve procurement of chemicals, columns, and instrument spares. 5. Regulatory and Customer Interaction Respond to regulatory/customer queries. Initiate additional studies for vendor qualification and regulatory/customer needs. Implement new systems/procedures in line with regulatory guidance. 6. Team Management and Training Participate in recruitment for QC lab personnel. Conduct periodic training and evaluation of QC analysts. Participate in cross-functional investigations (product failures, complaints, deviations). 7. Budgeting and Vendor Management Prepare and manage revenue and capital budgets for QC. Evaluate new vendors for lab consumables. 8. Change Control Approve and oversee change controls and provisional process changes. Ensure proper documentation and closure post-implementation. Delegation Protocol In Absence: Responsibilities delegated to Head Lab-Operations and Head Lab-Compliance. Upward Delegation: Head QC Operation and Site Quality Head. Downward Delegation: Tactical/operational responsibilities to direct reporters. Person Profile . Qualification - Msc /Ph.D (Chemistry/Chemical/PCM/Bio-Chemistry) Experience- 15+ Years of relevant experience from API industry only Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, Please visit our LinkedIn Page- https://www.linkedin.com/company/jubilantpharmova/mycompany/
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 and 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 Biosys Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radio pharma, Allergy Immunotherapy, CDMO Sterile Injectable, Contract Research Development and Manufacturing Organisation (CRDMO), Generics and Proprietary Novel Drugs businesses. In the Radio pharma 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 Injectable business offers manufacturing services including sterile fill and finish injectable (both liquid and lyophilisation), full-service ophthalmic offer (liquids, ointments and 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 Biosys Limited Designation - Associate Director / Director - Business Excellence Location- Nanjangud, Mysore Job Summary - Key Responsibilities. Partner with Leadership team and site leadership team to ensure the best use of resources in defining and planning site targets, KPI and #39;s, objectives and programs to achieve the strategy aligning with the API Operations Unit. Align with various stakeholders and leadership, prioritize, create and own project specific plans to drive improvement initiatives. Provide leadership and demonstrate ability to coach at the SLT level and across the broader organization Ensuring safety, quality, delivery, and cost is achieved to support business strategy. Build, test, and analyze business cases for long range strategic opportunities. Provide strategic link with business excellence. Direct and deploys the Project Management Office. Lead the strategy deployment process at site/function to understand strategy and support translation into AGILE activities in roadmap and ensure the learning site processes are aligned with the global learning strategy. Evaluation, update and revisions of project plans and bring more visibility to meet project deadlines Coach and lead the deployment of Lean and Six Sigma process within the respective site Provide constant education and upskilling of delivery staff on concepts of process improvement methodologies, RCAs, Delivery framework, analytics etc Initiate and coordinate AET's in plants as a part of Cultural Transformation initiative in Production Blocks of the Site Support People end to end on the Task force and Sankalp Initiative Drive People engagement at shopfloor by establishing Gemba Culture. Person Profile : B. E / B. Tech (Pref in Chemical) with 18+ years of experience in Chemical Plant, Petrochemical Plant and large integrated organic Chemical plants. Experience of managing multi-sites operations. Knowledge of Chemical process and plant design. Practical knowledge of Kaizen, Value Engineering, SPC, and Lean Six Sigma. Knowledge and strong exposure to occupational health, safety and environment practices. Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, Please visit our LinkedIn Page- https://www.linkedin.com/company/jubilantpharmova/mycompany/
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 and 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 Biosys 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 and 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 Biosys Limited Designation - Chemist / Officer -;Production Location- Nanjangud, Mysore Job Summary - Key Responsibilities. Equipment handling: Operation and Cleaning of Equipment's used in the process area. Trouble shooting of the equipment's during process. Production Planning: Manufacturing and packing of the products as per BMR / BPR. Material Handling: Consumption of Raw and packing material and solvents in shop floor. Safety, health and environment: On line monitoring of the environment conditions in process area. Desired Certifications: cGMP certificates, Ms Office, SAP preferred Functional Skills: Handling of unit operations and unit process. Documentation capabilities like filling of BMR / BPR/BCR etc. Knowledge of basic cGMP Critical thinker Problem solving attitude Attention to details Handling manpower in Shop-floor Planning of day to day activity General Awareness : Knows the fundamental or has general understanding of concepts. Working Knowledge : Has broad job knowledge, knows to apply the full range of concepts and practices and has broad/working knowledge of the subject. Candidate should use these concepts in day to day practices. Person Profile . Qualification- Graduate in B.E Chemical Engineering/BSC (Chemistry/PCM/Bio chemistry)/Diploma Chemical Engineering Experience- 2 + Year of relevant experience from any API industry. Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, Please visit our LinkedIn Page- https://www.linkedin.com/company/jubilantpharmova/mycompany/
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 and 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 Biosys 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 and 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 Biosys Limited Designation - Deputy Manager - Statutory Compliance Location- Nanjangud, Mysore Responsible for following activities: Contract labour Management: Ensure all documents relating to compliance with Statutory and other provisions shall be available with the contractor at all times obtained from the competent authority, Ensure monthly statutory compliance of contractors including ESI and PF remittance, Half-yearly and Annual returns etc., Processing and checking the bills of the contractors who are providing Manpower services, Ensure the validity of contractor's license obtained from competitive authority, Ensure contract labours Biometric Attendance. Ensure annual approved budget to deploy the contract labours and raise the PO for the same. Co-ordinate with the SCM for CPG approval as and when required and, ensure the validity of Contractor agreement. Wage break up of all Manpower Supply contractors, NAPS and Outsourced as per The Minimum Wages Notification. Ensuring CPG Approval, PR and PO of all Manpower Supply Contractors. Statutory Compliance: Comply with the statutory compliance under the provisions of Labor Laws like the Contract Labour (R and A) Act, 1970, Employees Provident Funds and Misc. Provisions Act, 1952, Factories Act, 1948, Industrial Disputes Act, 1947, Workmen's Compensation Act, 1923, Maternity Act, 1961, Payment of Bonus Act,1965, Payment of Gratuity Act, 1972, Minimum Wages Act, 1948, Payment of Wages Act, 1936 etc. and any other Law / Legislation which may be applicable from time to time. Submission and ensuring monthly, quarterly, half yearly and Annual Returns under various Labour Laws, letter correspondence / co coordinating with different Departments. Updation and amendment of License and CLR (Addition and Deletion of Directors, Change of Factory Manager). Co-ordinate with corporate team who are handling the EPF to address the employees PF issue on time, Process and settle gratuity payout of the eligible employees. Ensuring IT Returns (Under Section 5) of Employees Gratuity Trust. Ensure the NAPS recruitment activity and its compliance. Update the statutory / compliance status in conformity tool. Submission of Form No 11 of New Joiners on a weekly basis (Cross Checking the PF Data). Submission of required inputs to HO for generation of new joiner's TIC under ESIC. Ensuring monthly pension under EPFO of retired employees and employees who attained superannuation. Pay Roll and IR Support Function: Share PLIS, LTA provision to finance on monthly basis, Collect the data on Technicians Annual Performance Appraisal and its calculation. Prepare the data for yearly Bonus and Ex gratia payment and provision to finance monthly basis. Preparation of monthly MIS related to Contract Employees Man-days and BPR (Attrition) data. Preparation of MIS of Onroll Employees. Arrears calculation and salary components changes related to technicians post LTS. VDA changes input once in a three months. Grade benefit input and its calculation once in a year. Technician's Promotions and its calculation once in a year. Anaplan - Both Offroll (NAPS, Outsourced and Contract Employees) and Onroll (Executive). Monthly Budget CTC vs Actual CTC report. Providing Birthday and Anniversary data to the Admin Department. Translation of MOM in local language. Health Insurance Co-ordinate with the Health Insurance TPA to facilitate employees to avail Health Insurance service.; Ensuring updation of Family Member details in Darwin Portal. Person Profile. Education Qualification (Highest) with Target Institute(s): MSW/MBA Human Resources Experience Range : 13+ years
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 and 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 Biosys 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 and 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 biosys Limited Designation ; - Manager- Procurement Location ;;;; - Nanjangud, Mysore Key Responsibilities: Shall be responsible for the following activities: Procurement of raw materials, Packing material, solvents and Acid tankers. Identification of new sources to mitigate single source dependency Coordinating with vendors and negotiating the right price, quality and timelines. Ensure the payments to all vendors and service providers. Coordinating with logistics and service providers. Ensure GMP and regulatory compliance. Meet the RM Delivery schedule and ensure sequence production in terms of RM Supply. Monitoring inventory and schedule deliveries. Sale of non-moving materials Yearly Agreement for transporter contractors External manufacturing actives Service bills processing Renewal of Certifications {UN Drums} Vendor rating as per SOP Verification and scrutiny of vendor quality documents, forwarding to QA and monitoring the qualification process with IP, QA, QC, R and D and RA. Alternate vendor development Vendor re qualifications as per SOP Review and approval of QMS documents Handling of CDMO projects Requirement: Qualification: BSc/MSc - Chemical Engineering Purchase experience: 10+ years Pharma - API. Experience in procurement of KSM, Intermediate, Chemicals, Solvents and Catalogue chemicals Handled procurement of: 400 Cr per annum.
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 and 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 Biosys 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 and 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 Biosys Limited Designation - Analytical Research R and D Location- Nanjangud, Mysore Key Responsibilities. Responsible for the preparation, execution and review of Analytical method validation, method transfer, specifications, test methods, technical packages (part-D), analytical studies protocols, and respective reports. Planning and timely completion of the analysis of HPLC, NMR and XRD samples. Analysis of various in-process, intermediates and finished product samples of pilot plant trail and experimental batches and recording of results. Conducting Laboratory investigation during incidents / deviations. Preparation and standardization of volumetric solutions. Calibration of various analytical instruments as per the schedule. Preparation and completion of documents pertaining to products. Online entry in analytical Equipment Usage log. Analysis of the samples received from marketing/purchase/outside and reporting. Attending in the shifts to support operation of the lab activities. Maintain good housekeeping in lab. Support for absence studies, additional studies and Cleaning validations. Preparation and review of SOP's related to quality systems. Reviewing all the analytical data, documents and ensuring that same are completed and signed. Coordinating with service engineers for the rectification of the instruments during break down. Conducting the investigation for the laboratory incidents and deviations. Responsible for checking/reviewing the analytical data and verification. Responsible to handle the QMS in Trackwise. Person Profile. Education Qualification: Post Graduate in Science/ Doctorate Experience Range : 3+ years in Analytical R and D Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, Please visit our LinkedIn Page- https://www.linkedin.com/company/jubilantpharmova/mycompany/