Co-ordination with internal as well as external customer for smooth Functioning of stores. Responsible for issue of material to various customers as per requirements. Procurement of Material, Consumables and services Responsible for finished goods inventory as per book stock. Verification of stock (books vs. physical). Preparation of MRN for all the receipts. Functional Skills Conceptual knowledge of Inventory management Conceptual knowledge of ISO standards, WCM Proficiency in MS-Excel / MS word or like software Knowledge of using ERP. General Awareness: Knows the fundamental or general understanding of concepts. Working Knowledge: Has broad job knowledge; knows and applies the full range of concepts and practices. Has broad / working knowledge of the subject. Candidate should use these concept in day to day practices.

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:

Conduct financial analysis and modelling to support investor relations activities. Monitor and analyse competitor investor relations activities, market dynamics, and trends to inform strategic planning and positioning. Assist in the preparation of quarterly and annual reports, investor presentations, and other communication materials Maintain and update investor databases and contact lists. Manage investor inquiries and provide accurate and timely information. Collaborate with internal teams, including finance, legal, and communications, to ensure consistent messaging and compliance with regulatory requirements. Person Profile . Qualification - MBA/ CPA, CFA, or CMA. Experience 4-6 Years of experience in investor relations, financial analysis, Must Have - Strong understanding of financial statements and market data. Proficiency in financial analysis and modelling. Excellent communication and presentation skills. Ability to prepare detailed reports and investor materials. Proficiency in MS Office applications, including Excel, PowerPoint, and Word. Experience with investor relations software and databases. Knowledge of industry-specific regulations and compliance requirements . Jubilant is an equal opportunity employer.

Design and plan synthetic routes for target molecules. Execute multi-step organic synthesis reactions, handling milligram to gram scale reactions. Characterize organic compounds using spectroscopic and related techniques. Perform literature searches using scientific databases (e.g., SciFinder). Solve synthetic challenges and troubleshoot issues. Maintain accurate records, including electronic laboratory notebooks (eLNB) and data integrity.

Cell based assay development (optimization, validation and compound screening) Enzyme based assay development (optimization, validation and compound screening) Invitro assay development, validation and optimization of cell based assay and enzyme based assay for various targets in the respective therapeutic areas such as CNS/ Metabolic disorder/ Autoimmune/Inflammatory diseases/ Pain/Oncology in Drug Discovery field. Developing and optimizing assays. Regular screening of compounds. Working extensively in the area functional cell based assays, validated the same to determine the activity of new chemical entities (NCEs). Engineering stable and transient cell-lines. Setting up platforms for interrogating compounds and Platform development for target engagement models. ",

Lay out plan for movement of material Preparation of Delivery challan , E way Bill, Inventory management LN system inventory reconcilation / DDR Reporting MIS/Books Closing , Booking of expenses related to port operation bills IMPORT AND DISPATCH PLAN Space management, NOC from shipping line, NOC from storage Tank , Cordination with CHA, Shipping Line, Tanks Frams, Serveyor

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:

Manager TPM/TQM Business Unit / Function Jubilant Ingrevia/BE Location Bharuch Reports to Site -BE Lead and Dotted matrix reporting to Site head Summary of Job (Purpose/ objective of the job Department organogram to be enclosed) To establish TQM/TPM culture in the plant/site Key Responsibilities (Performance Indicators) Work closely with teams to implement TQM/TPM and ensure its sustenance Coach and Mentor the employees for Total Employee participation in the continuous improvement Form Quality Circles and lead daily/weekly meetings and Identify KPI s for Quality Circle and link to business goals Perform TQM process audits, address gaps and implement necessary actions Train and lead the teams for problem solving Collaborate with steering committee for TQM/TPM progress Improve QMS through internal and external audits Ensure that all associated employees work toward the common goals of improving product Quality-centric culture where every employee feels responsible for maintaining quality standards. No. of Reportees NA Qualification & Experience B.Tech/MBA and Certified in ASQ s Total Quality Management/ Certified TPM Practitioner Key Competencies ( Technical, Functional & Behavioral) Min 10-15 years experience into TQM/TPM Implementation Ability to train and lead the teams on problem solving Effective communication and presentation skills Ability to collaborate with cross functional teams Proficiency in computer specifically MS office Excellent Knowledge TQM/TPM process

Having exposure of 1-4 years in analytical chemistry, method development and analysis of regular samples on chromatographic instruments (LC-MS). Candidate should be well acquainted with the respective instrument and software. Maintenance, cleaning, documentation and calibration of analytical instruments. Demonstrate perseverance, team co-ordination and analytical approach at the work place. Should be flexible with working hours. Provide training to new joiners. Practice safe work habits including complying with all safety health and environmental rules and regulations Person Profile Qualification: - M. Sc. (Analytical Chemistry)/ M. Pharm or related field from reputed university/institute. Experience: - 1-4 years of relevant experience for Masters.

Preparation/review and submission of new dossiers and updates for global markets. Preparation/review and submission of responses to queries from regulatory authorities/customers. Provide technical regulatory support to CRD for various activities (route of synthesis, starting material designation, specifications design, applied testing methodologies, Analytical method validations) related to new product development and other regulatory issues as they arise. Review of R&D technical packages for new product development (NPD) as well as cost/quality improvement process (CIP/QIP) for regulatory adequacy. Coordination with R&D to discuss on process and product controls, quality, patent and special studies to respond the queries from regulatory authorities/customers. Tracking of activities status to meet the timeline for new Submissions, Responses and Life cycle management of Dossiers. Preparation/review and submission of technical packages and open parts as per customer requirement. Review of technical packages for out sourced starting materials and intermediates for regulatory adequacy. Review of analytical method validations, characterization data, process validations, analytical data, specifications/test methods, BMRs, packing material details, and stability data etc. w.r.t. regulatory adequacy for dossier compilation. Review of CSO/stability protocols [EDMS] and change controls (track-wise) related to facility, manufacturing process and control of materials etc. for regulatory adequacy. Attending to on the job trainings and off the job trainings . Updating health authority new guidelines to Regulatory affairs team. Person Profile. Education Qualification: MSc / M.Pharma,/ B.Tech / M.Tech in Chemical

Preparation/review and submission of new dossiers and updates for global markets. Preparation/review and submission of responses to queries from regulatory authorities/customers. Provide technical regulatory support to CRD for various activities (route of synthesis, starting material designation, specifications design, applied testing methodologies, Analytical method validations) related to new product development and other regulatory issues as they arise. Review of R&D technical packages for new product development (NPD) as well as cost/quality improvement process (CIP/QIP) for regulatory adequacy. Coordination with R&D to discuss on process and product controls, quality, patent and special studies to respond the queries from regulatory authorities/customers. Tracking of activities status to meet the timeline for new Submissions, Responses and Life cycle management of Dossiers. Preparation/review and submission of technical packages and open parts as per customer requirement. Review of technical packages for out sourced starting materials and intermediates for regulatory adequacy. Review of analytical method validations, characterization data, process validations, analytical data, specifications/test methods, BMRs, packing material details, and stability data etc. w.r.t. regulatory adequacy for dossier compilation. Review of CSO/stability protocols [EDMS] and change controls (track-wise) related to facility, manufacturing process and control of materials etc. for regulatory adequacy. Attending to on the job trainings and off the job trainings . Updating health authority new guidelines to Regulatory affairs team. Person Profile. Education Qualification: MSc / M.Pharma,/ B.Tech / M.Tech Chemical Engineering Experienc e Range : 10+ years in API Regulatory Affairs Jubilant is an equal opportunity employer. .

At least a year experience in handling HPLC analysis Should have experience in handling empower application software Must have knowledge of LIMS operation In depth knowledge on document practices ALCOA++ Should know the procedure for lab incident, deviation and OOS management Should adhere to the testing SLA Should adhere to the SOPs and policies all time Should adhere to data integrity policy all time Should record all the testing results and log books as per respective SOP Should complete training as per the schedule Preference will be given to candidates who have involved/ participated in Design and qualification of LIMS Person Profile. Education Qualification: Degree in Science/ Post Graduate in Science (Chemistry)/ Bachelor of Pharmacy/ Master in Pharmacy and Doctorate Experience Range : 1-5+ years

Responsibilities Achievement of set targets. Maintaining set call Average/coverage. Complete use of allotted resources. Increasing prescriber base Focus on target customers. Maintaining call average and customer coverage Increasing PCPM. Timely reporting. Ensuring ROI Competencies Proficiency level Convincing ability Presentation Selling Communication Behavioral Analytical ability PR Skills

Responsibilities Achievement of set targets. Maintaining set call Average/coverage. Complete use of allotted resources. Increasing prescriber base Focus on target customers. Maintaining call average and customer coverage Increasing PCPM. Timely reporting. Ensuring ROI Competencies Proficiency level Convincing ability Presentation Selling Communication Behavioral Analytical ability PR Skills

Responsibilities Achievement of set targets. Maintaining set call Average/coverage. Complete use of allotted resources. Increasing prescriber base Focus on target customers. Maintaining call average and customer coverage Increasing PCPM. Timely reporting. Ensuring ROI Competencies Proficiency level Convincing ability Presentation Selling Communication Behavioral Analytical ability PR Skills

Shall be responsible for the following activities: Complete the allocated projects (NPD, CIP/QIP and KSM) with desired yield and quality within given timeline Find out the risk associated in each steps w.r.t. Yield, quality and EHS and find out the CPP Co-ordinate with team and group leader, keep them informed about the progress of progress of projects and issue that are being faced and find out the solution Understand the requirements of process, anticipate molecule development issue, if any, and take necessary steps to avoid it. Co-ordinate with pilot plant for demo, process discussion etc. Synthesis of impurities as per requirements. Investigate the failure of batches and come up with action plan. Preparation of SOP is as and when required and ensure that the analysts have read, understood. Ensure compliance and enforcement of SOPs and safety policies in group. Follow & Maintain GLP, GMP, Safety in Lab Delivering of work/ instructions given by concerned project group leaders to carry out the assigned job as per scheduled plan and safety precautions. Regularly exercise of experiments interpretation of experimental results. Co-Ordinate with team and team leaders, keep them informed about the progress of projects and issue that are being faced. Also need active involvement in brainstorming session. Documentation of experiments in Lab record as and when the experiments is completed. Preparation and review of the reports, Process outlines, Technical packages - B and C and support for the scale up and validations in pilot plant/plant. Ensuring the experimentations are carried out as per norms and safety precautions Responsible for performing research and development experiments for the project in collaborations with others Investigate the failure of batches and comes up with the action plan Provide demo process to the tech-transfer team in pilot plant To work in the shifts and take care of the lab safety precautions Ensuring the Equipment/ area is cleaned before use To maintain the good Housekeeping Person Profile. Education Qualification: Post Graduate in Science/ Doctorate Experience Range : 0-1years

Accountabilities Scope of work Organic Chemistry Leverage on past exposure and handle the project and measure their success through numbers (Projects / People) handled molecules generated and problem tacked etc. Responsible for project management and designing the alternate and feasible route for synthesis so that the project completed within the given time frame and solving the problem of chemist to achieving the target. Optimizing the resource qualitatively and quantitatively according to project priorities and sage of development. Team Management Able to handle the team 15 25 people including second line manager. Team member career growth. Reporting Project update and interaction with client, support in recruitment process. External Interfaces Internal Interfaces Safety, cost-effective work, maintaining lab Synthesis, purification skill Education Experience: Indicate the education level, previous experience, specific knowledge, skills and abilities required to meet minimum requirements for this Job. Education Qualification(Highest ) with Target Institute(s) Ph. D

Jubilant Biosys is looking for Immediate Joiners. Research Associate - Organic Synthesis - Discovery Chemistry - Bengaluru location Experience: 3-7 Years Qualification: M.Sc. (Organic/ General/ Industrial Chemistry) M. Pharm (Medicinal Chemistry) Design and plan synthetic routes for target molecules. Execute multi-step organic synthesis reactions, handling milligram to gram scale reactions. Characterize organic compounds using spectroscopic and related techniques. Perform literature searches using scientific databases (e.g., SciFinder). Solve synthetic challenges and troubleshoot issues. Maintain accurate records, including electronic laboratory notebooks (eLNB) and data integrity.

Jubilant Biosys is looking for Senior Research Associate - Discovery Chemistry - Bengaluru location Experience: 5-7Years Qualification: M.Sc. (Organic/ General/ Industrial Chemistry) M. Pharm (Medicinal Chemistry ) Design and plan synthetic routes for target molecules. Execute multi-step organic synthesis reactions, handling milligram to gram scale reactions. Characterize organic compounds using spectroscopic and related techniques. Perform literature searches using scientific databases (e.g., SciFinder). Solve synthetic challenges and troubleshoot issues. Maintain accurate records, including electronic laboratory notebooks (eLNB) and data integrity. ",

Jubilant Biosys is looking for Manager Power Portfolio Mgt to join our dynamic team and embark on a rewarding career journey. Delegating responsibilities and supervising business operations Hiring, training, motivating and coaching employees as they provide attentive, efficient service to customers, assessing employee performance and providing helpful feedback and training opportunities. Resolving conflicts or complaints from customers and employees. Monitoring store activity and ensuring it is properly provisioned and staffed. Analyzing information and processes and developing more effective or efficient processes and strategies. Establishing and achieving business and profit objectives. Maintaining a clean, tidy business, ensuring that signage and displays are attractive. Generating reports and presenting information to upper-level managers or other parties. Ensuring staff members follow company policies and procedures. Other duties to ensure the overall health and success of the business.