Role: Assay Biologist Department: Biology Location: Hyderabad About Us: Sai Life Sciences is one of the fastest-growing Contract Research, Development, and Manufacturing Organizations (CRDMOs). As a pure-play, full-service partner, we collaborate with over 300 global innovator pharma and biotech companies to accelerate the discovery, development, and commercialization of their NCE programs. We have over 3000 employees across our facilities in India, the UK, and the USA, working together to deliver scientific excellence and customer success. We are a Great Place to Work certified organization with a culture of openness, mutual respect, and inclusivity. We embrace diversity and follow equal opportunity practices across all levels. Summary of Job: Knowledge on biochemical and cell-based assays. Key Responsibilities : Execute assay optimization, validation, and compound screening in various in vitro biochemical and cell-based assays. For cell-based assays hands on following is desirable: Ø Media preparation Ø Cell culture (Suspension and Adherent) Ø Cell cryopreservation Ø Cell seeding using automated dispensers Ø Compound dilutions, manually or using Echo Ø Hands on multimode microplate readers such as Envision and FLIPR For cell free (biochemical) assays understanding of following is desirable: Ø Enzyme kinetics Ø KM Ø Assay optimization parameters Ø Different assay technologies for kinase assays Analyse and interpret the data from assay optimization, validation, and compound screening studies. Record the experimental data in prescribed format in LNB and or ELN Operate instruments for efficient, accurate and reproducible data. Use analysis software/s for data handling (GraphPad Prism). Familiar with the current assay techniques (HTRF, AlphaLISA, Luminescene, Fluorescence, Absorbance.) and assays (Reporter gene assays, FLIPR assay, CTG assay, ADP Glo kinase assay, etc) Execute compound management procedures, indenting process, receiving, maintenance of reagents and consumables stocks. Adhere to and follow Sai policies and company rules. Experience/Qualification: M.Sc/M.Tech/M.Pharm with 2-3 years of relevant industry experience. Key Competencies (Technical, Functional & Behavioural): Technical: Multi-channel pipettes, Multimode plate readers, Western blot apparatus, operation of centrifuge, ELISA etc. Functional: Basic knowledge on biochemical and cell-based assays. Behavioural : Team player, ability to work with multidisciplinary teams. Strong analytical skills and ability to work under stringent timelines, good communication skills.

Key Responsibilities: Process vendor invoices (PO-based & Non-PO) with accuracy in ERP (e.g., Oracle/SAP). Ensure proper matching of Purchase Order, GRN, and Invoice (3-way match). Coordinate with Procurement, Stores, and Production for invoice clarifications or discrepancies. Ensure timely GST input validation and TDS deduction during invoice processing. Track advance payments and ensure timely adjustments. Prepare vendor ageing reports and reconcile vendor ledgers regularly. Support monthly closure activities – provisioning and expense accruals. Assist in vendor query resolution and payment status communication. Maintain proper documentation and audit trail for invoices and payments. Adhere to company’s internal controls and SOPs in accounts payable function. Qualifications & Skills: B.Com / M.Com / CA Inter preferred. 3–5 years of experience in accounts payable in a manufacturing company. Strong knowledge of GST, TDS, and payment cycles. Hands-on experience with Oracle/SAP or other ERP systems. Proficient in MS Excel, especially pivot tables and VLOOKUP.

Summary of Job To be responsible for pre-formulation and preclinical formulation activities. To be responsible for designing the experiment under supervision and handling associated equipment's and operations along with interpretations. Key Responsibilities 1.Ability to design and execute pre-formulation experiments like solubility, pKa, log P, dissolution, intrinsic dissolution, bulk density, flow indices, solid-state assessment, excipient compatibility etc. 2.Completely conversant with hands on experience and/or interpreting data from pre-formulation studies of a compound including physicochemical, bulk, surface and particle properties. 3.Ability to design and execute preclinical formulations to support lead ID, lead optimization and clinical candidate selection, including but not limited to solution, suspension, powder for constitution, compound filled in capsules and basic tablet ability. 4.Reasonably conversant with hands on experience and/or interpreting data from solid-state equipment's like PXRD, MDSC, TG, DVS and other techniques like Polarizing and Hot-stage Microscopy and other dynamic image analysis techniques, specially during supporting solid form and salt screening. 5.An additional benefit would be to have operational experience of handling Particle size analyzer, HPLC, GC, Dissolution apparatus and Disintegration apparatus. 6.Ability to collate and scientifically present data & observations and provide scientific inputs in discussion with internal or external customers. 7.Proactively maintain the equipment's, facility and supporting systems as per established good lab handling processes, maintain requisite equipment and process SOPs and lean tools 8.Follow good documentation practices and have adequate exposure to record observations in Electronic Lab Notebook (ELN). 9.Proactive in aligning with new technologies and approaches to participate in continuous improvement needs of the business. 10.He/she should have sufficient knowledge chemical safety, comprehensive risk assessment of drug substance and safe handling. Qualification M. Pharma, M.Sc. or M Tech with relevant specialization in Pharmaceutical Sciences Experience 1-5 years Key Competencies (Technical, Functional & Behavioral) Technical & Functional Sound experience of fundamentals of pre-formulation and approaches used for preclinical formulation development of compounds. Basic knowledge on developing clinical formulation would be an added plus. Demonstrated capability in having understanding to design and interpret data from PXRD, modulated DSC, TGA, DVS, Microscopy and working operations of HPLC, GC, FT-IR, NMR, Dissolution, BET and other physical and physicochemical characterization techniques. Hands-on operating would be an added plus. Behavioral Aptitude to learn and excel. Proactive in technical & operational space. Ability to work in cross-functional team environment. Ability to contextualize the observations and attention to detailing. Effective communication skills and absorbing attitude.

Key Responsibilities: Responsible for coordinating with Process R&D and Technology Transfer teams related to new projects to be initiated in Production Block-07. Responsible for verification of the new projects initiated in Production Block07 with respect to desired intend in perspective of Quality, Yield, Batch Cycle Time, Safety, etc. Responsible for all the process operations of Production Block-07 by maintaining the compliance with respect to Safety and Quality. Responsible for preparation & review of production schedule in-line with committed targets. Responsible to deliver the products in accordance with production plan by considering the specific requirements of the customers. Responsible for handling the manpower belongs to Production Block-07 and deploying the work to them as per their roles and responsibilities. Responsible for ensuring the standard operating procedures are being followed on shop floor without any deviations and enforcing the same consistently. Responsible to prepare, review and revise the Standard Operating Procedures for all operations & systems from time to time with the support of Quality Team. Responsible for ensuring the process operations are carried out as per the batch production records with proper safety measures. Responsible for coordinating with service departments & ensuring the activities bearing to service departments are completed as per stipulated time. Responsible for maintaining & monitoring the Good Housekeeping Practices in process areas and sustaining 5S practices. Responsible for all QMS (Quality Management System) documents & its authentication belongs to Production Block-07. Responsible for initiating, reviewing the documents like BPRs, change controls, deviations, investigations and ensuring the timely closure of it as per the procedure. Responsible for carrying out the discussions with cross functional teams in case of any process failures or customer complaints, preparing & reviewing the investigation reports and implementing the suitable CAPA. Responsible to prevent failures from re-occurrence by thoroughly investigating the problem to find an exact root cause to achieve quality at Right First Time (RFT). Responsible to maintain all previous campaign details to review the quality & quantity trends in reference to the process operations and ensure the consistency for the same. Responsible to maintain & manage the inventories & operational expenses of the plant through periodic review. Responsible to train & motivate the team on better work methods, safe operating procedures, cGMP, Business Excellence Initiatives. Responsible to ensure internal & external audit compliance with respect to safety & quality. Responsible to motivate the team for improvements projects like Cost Reduction, Capacity Enhancement and Operation & Quality improvement. Responsible for solvent related activities like stock verification, spent disposal, solvent treatment, emission control, etc. Responsible to participate Behavior Based Safety (BBS) programs and enforce & train the team to report all safety related events/ incidents immediately without delay. Responsible to prepare & review the qualification and validation documents like VMP, URS, DQ, IQ, OQ and PQ in-line with regulatory guidelines. Responsible to prepare a& review HSE documents like process & facility Hazop, Also ensuring the work permit system is strictly followed in the Production Block. Key Competencies (Technical, Functional & Behavioral) Technical & Functional: Good communication skills Demonstrate ownership and collaboration at work Primary Responsibilities: Responsible for Co-Ordinating with Process R&D and Technology Transfer teams related to new projects to be initiated in Production Block-07.

Role: Assay Biologist Department: Biology Location: Hyderabad About Us: Sai Life Sciences is one of the fastest-growing Contract Research, Development, and Manufacturing Organizations (CRDMOs). As a pure-play, full-service partner, we collaborate with over 300 global innovator pharma and biotech companies to accelerate the discovery, development, and commercialization of their NCE programs. We have over 3000 employees across our facilities in India, the UK, and the USA, working together to deliver scientific excellence and customer success. We are a Great Place to Work certified organization with a culture of openness, mutual respect, and inclusivity. We embrace diversity and follow equal opportunity practices across all levels. Summary of Job: Knowledge on biochemical and cell-based assays. Key Responsibilities : Execute assay optimization, validation, and compound screening in various in vitro biochemical and cell-based assays. For cell-based assays hands on following is desirable: Ø Media preparation Ø Cell culture (Suspension and Adherent) Ø Cell cryopreservation Ø Cell seeding using automated dispensers Ø Compound dilutions, manually or using Echo Ø Hands on multimode microplate readers such as Envision and FLIPR For cell free (biochemical) assays understanding of following is desirable: Ø Enzyme kinetics Ø KM Ø Assay optimization parameters Ø Different assay technologies for kinase assays Analyse and interpret the data from assay optimization, validation, and compound screening studies. Record the experimental data in prescribed format in LNB and or ELN Operate instruments for efficient, accurate and reproducible data. Use analysis software/s for data handling (GraphPad Prism). Familiar with the current assay techniques (HTRF, AlphaLISA, Luminescene, Fluorescence, Absorbance.) and assays (Reporter gene assays, FLIPR assay, CTG assay, ADP Glo kinase assay, etc) Execute compound management procedures, indenting process, receiving, maintenance of reagents and consumables stocks. Adhere to and follow Sai policies and company rules. Experience/Qualification: M.Sc/M.Tech/M.Pharm with 2-3 years of relevant industry experience. Key Competencies (Technical, Functional & Behavioural): Technical: Multi-channel pipettes, Multimode plate readers, Western blot apparatus, operation of centrifuge, ELISA etc. Functional: Basic knowledge on biochemical and cell-based assays. Behavioural : Team player, ability to work with multidisciplinary teams. Strong analytical skills and ability to work under stringent timelines, good communication skills.

Summary of Job Liasoning and Recording of Logistic & IT invoices and having good relationship with stake holders Key Responsibilities Booking of Invoices with Proper verification Vendor Reconciliation & Balance confirmation statement preparation Handling stake holders Knowledge of GST/TDS and other compliances Knowledge of Agreement and 3 Way match concept Qualification M.Com/MBA (Finance)/CA Inter/ICWA Inter Experience Atleast 3 to 4 Years of Experience on Invoice booking (Pharma Sector & Oracle Finance Experience is extra advantages) Key Competencies (Technical, Functional & Behavioural) Sound skill of MS Office (Excel, Word, Outlook & Power point) Accounting Software (Oracle preferable)

Summary of Job Liasoning and Recording of Logistic & IT invoices and having good relationship with stake holders Key Responsibilities Booking of Invoices with Proper verification Vendor Reconciliation & Balance confirmation statement preparation Handling stake holders Knowledge of GST/TDS and other compliances Knowledge of Agreement and 3 Way match concept Qualification M.Com/MBA (Finance)/CA Inter/ICWA Inter Experience Atleast 3 to 4 Years of Experience on Invoice booking (Pharma Sector & Oracle Finance Experience is extra advantages) Key Competencies (Technical, Functional & Behavioural) Sound skill of MS Office (Excel, Word, Outlook & Power point) Accounting Software (Oracle preferable)

Ø Follow-up with Buyers and End Users to get the import documents for all Medchem, DMPK and Biology shipments. Ø Coordination with Carriers/CHA on shipments documentation. Ø Shipment Documents Verification, Checklist approvals and Sharing shipment documents with Stores for shipment handover process. Ø Follow-up with carriers and Brokers to clear the shipments on-time and get the post shipping documents. Ø Maintaining MIS data related to Export and Import shipments. Ø Daily import and export tracker should be sent before EOD to all the stakeholders. Ø Collecting the Billing/Non Billable data for all Export and Import shipments. Ø Handing over of the freight forwarder/carrier bills to Finance and follow-up with them for payments. Ø Maintain Billing data and submit Bills with all corresponding supporting documents.

Sr Executive/Asst Manager Role: 5–8 years of procurement experience in a pharmaceutical/CRO/CDMO - preferably in the biology domain. Key Responsibilities: Source and procure biology-related consumables, reagents, lab supplies, assay kits, cell lines, as per project requirements. Interact with scientific stakeholders (biology team) to understand technical requirements and ensure procurement aligns with research timelines. Identify, evaluate, and onboard qualified suppliers while maintaining compliance with regulatory and internal procurement standards. Request and evaluate quotations, negotiate with vendors, and raise purchase orders in the ERP system (Oracle). Track order status, coordinate logistics, and ensure timely delivery. Maintain procurement documentation, including quotations, order confirmations, delivery challans, and invoices. Work closely with Sai Boston procurement team ,Stores and Finance teams for MRNs, invoice processing, and vendor payment follow-ups. Monitor vendor performance and develop supplier relationships to ensure continuous quality improvements and cost savings. Required Skills and Qualifications: Bachelor’s or master’s degree in science (preferably Biology/Biotechnology) or equivalent. Knowledge of sourcing lab consumables, reagents, instruments, and equipment. Familiarity with procurement tools - ERP Oracle Strong negotiation, communication, and vendor management skills. Ability to work independently and collaboratively with cross-functional teams. Basic MS office reporting skills

Summary of Job: To support a team of 25-35 scientists and taking comprehensive responsibility of on time Analytical support for projects with minimal or no supervision. Role requires complete ownership of the project, cross-functional team coordination. Key Responsibilities: oTo lead the LC-MS, Prep HPLC, HPLC and NMR teams and responsible projects delivery. oResponsible to understand the scope of project and scope changes, accordingly, providing guidance to the team. oResponsible to scientific review and interpretation of the analytical data to ensure the correctness and quality. oProject execution support, as required: Providing scientific guidance and resolutions to the team as and when needed. oTo review the data presented by Team Leaders (Three TLs, associated each by 6-10 scientists) and team and technically guides them further/suggest course correction, wherever required. oMonitor all the responsible projects, sample load, planning and ensuring to meet the TAT. oRegularly review the progress of the analytical TAT and work on the corrective actions. oTo be responsible for prescribed data generation, timely completion and review of Analytical results and data. oCommunication: Responsible for attending the client telecons wherever required 1.Cross-functional coordination: Should ensure the regular interactions with the chemistry team and other functional group like Sourcing team ( SCM), Operation excellence team. oQuotes: Providing the costing for analytical activities as per the project scope. oLaboratory maintenance: Ensure safety practices are in place, constant review of the lab requirements and upgrading. oDepartment initiatives – Take at least one initiative in the department to improve the department and Active participation in all management initiatives, group discussions. oCompliance: Comply with rules, guidelines, and trainings. Participate in general lab maintenance efforts and comply with regulated environment. oSafety: To ensure that appropriate personal protective equipment’s (PPEs), responsible for the safe working of the team in the laboratory and follows the safety precautions. oTeam management and development: Guide, train, and support team members to ensure quality work is delivered as planned. Ensuring proper distribution of tasks and resource utilization. Identify skills and mentor associates; assign responsibilities and follow up; feedback at regular intervals and maintain a record. Provide leadership and direct contribution to functional and/or cross-functional improvements. ExperiencePh.D. with more than 6 years or MSc with more than 8- 15 year’s experience in a API / CDMO Industry, of which minimum 5 years should be in CDMO.

Summary of Job: To support a team of 25-35 scientists and taking comprehensive responsibility of on time Analytical support for projects with minimal or no supervision. Role requires complete ownership of the project, cross-functional team coordination. Key Responsibilities: oTo lead the LC-MS, Prep HPLC, HPLC and NMR teams and responsible projects delivery. oResponsible to understand the scope of project and scope changes, accordingly, providing guidance to the team. oResponsible to scientific review and interpretation of the analytical data to ensure the correctness and quality. oProject execution support, as required: Providing scientific guidance and resolutions to the team as and when needed. oTo review the data presented by Team Leaders (Three TLs, associated each by 6-10 scientists) and team and technically guides them further/suggest course correction, wherever required. oMonitor all the responsible projects, sample load, planning and ensuring to meet the TAT. oRegularly review the progress of the analytical TAT and work on the corrective actions. oTo be responsible for prescribed data generation, timely completion and review of Analytical results and data. oCommunication: Responsible for attending the client telecons wherever required 1.Cross-functional coordination: Should ensure the regular interactions with the chemistry team and other functional group like Sourcing team ( SCM), Operation excellence team. oQuotes: Providing the costing for analytical activities as per the project scope. oLaboratory maintenance: Ensure safety practices are in place, constant review of the lab requirements and upgrading. oDepartment initiatives – Take at least one initiative in the department to improve the department and Active participation in all management initiatives, group discussions. oCompliance: Comply with rules, guidelines, and trainings. Participate in general lab maintenance efforts and comply with regulated environment. oSafety: To ensure that appropriate personal protective equipment’s (PPEs), responsible for the safe working of the team in the laboratory and follows the safety precautions. oTeam management and development: Guide, train, and support team members to ensure quality work is delivered as planned. Ensuring proper distribution of tasks and resource utilization. Identify skills and mentor associates; assign responsibilities and follow up; feedback at regular intervals and maintain a record. Provide leadership and direct contribution to functional and/or cross-functional improvements. ExperiencePh.D. with more than 6 years or MSc with more than 8- 15 year’s experience in a API / CDMO Industry, of which minimum 5 years should be in CDMO.

Ø Follow-up with Buyers and End Users to get the import documents for all Medchem, DMPK and Biology shipments. Ø Coordination with Carriers/CHA on shipments documentation. Ø Shipment Documents Verification, Checklist approvals and Sharing shipment documents with Stores for shipment handover process. Ø Follow-up with carriers and Brokers to clear the shipments on-time and get the post shipping documents. Ø Maintaining MIS data related to Export and Import shipments. Ø Daily import and export tracker should be sent before EOD to all the stakeholders. Ø Collecting the Billing/Non Billable data for all Export and Import shipments. Ø Handing over of the freight forwarder/carrier bills to Finance and follow-up with them for payments. Ø Maintain Billing data and submit Bills with all corresponding supporting documents.

Sr Executive/Asst Manager Role: 5–8 years of procurement experience in a pharmaceutical/CRO/CDMO - preferably in the biology domain. Key Responsibilities: Source and procure biology-related consumables, reagents, lab supplies, assay kits, cell lines, as per project requirements. Interact with scientific stakeholders (biology team) to understand technical requirements and ensure procurement aligns with research timelines. Identify, evaluate, and onboard qualified suppliers while maintaining compliance with regulatory and internal procurement standards. Request and evaluate quotations, negotiate with vendors, and raise purchase orders in the ERP system (Oracle). Track order status, coordinate logistics, and ensure timely delivery. Maintain procurement documentation, including quotations, order confirmations, delivery challans, and invoices. Work closely with Sai Boston procurement team ,Stores and Finance teams for MRNs, invoice processing, and vendor payment follow-ups. Monitor vendor performance and develop supplier relationships to ensure continuous quality improvements and cost savings. Required Skills and Qualifications: Bachelor’s or master’s degree in science (preferably Biology/Biotechnology) or equivalent. Knowledge of sourcing lab consumables, reagents, instruments, and equipment. Familiarity with procurement tools - ERP Oracle Strong negotiation, communication, and vendor management skills. Ability to work independently and collaboratively with cross-functional teams. Basic MS office reporting skills

Role: Documentation Department: Production Location: Bidar About Us: Sai Life Sciences is one of the fastest-growing Contract Research, Development, and Manufacturing Organizations (CRDMOs). As a pure-play, full-service partner, we collaborate with over 300 global innovator pharma and biotech companies to accelerate the discovery, development, and commercialization of their NCE programs. We have over 3000 employees across our facilities in India, the UK, and the USA, working together to deliver scientific excellence and customer success. We are a Great Place to Work certified organization with a culture of openness, mutual respect, and inclusivity. We embrace diversity and follow equal opportunity practices across all levels. Key Responsibilities : Drafting and Review of Investigation Reports in co-ordination with cross functional departments like Production Blocks, Maintenance, Process Engineering, QA, CQA, PR&D, QC and AR&D etc. Preparation of Quality Risk Assessment and its Impact Assessment Reports as or when required. Handling of documents related to Quality Management System (QMS) like Change controls, Deviations, Planned changes, CAPAs etc., as per requirement in co-ordination with cross functional departments like Production Blocks, Maintenance, Process Engineering, QA, CQA, PR&D, QC, AR&D etc. Follow the cGMP compliance by following the SOPs and approved procedures. Responsible for any activities assigned by HOD or Senior Management. Experience/Qualification: M.Sc/B.Tech/Diploma (Chemistry/Chemiscal) with 4-9 years of relevant industry experience. Key Competencies (Technical, Functional & Behavioural): 1. Must have GMP requirement and QMS knowledge. 2. Excellent written communication, interpersonal skills, data analysis and understanding of business processes.

JOB RESPONSIBILITIES: Overall Responsible for all the activities of the Warehouse department beside day –to- day activities Like Material Receipt, Issues, Distribution of Finished goods, Record/Documentation as per the C GMP Procedure as well as EOU statutory compliance. Responsible for upkeep of the quality system as per the c GMP in Ware house. Responsible For Continuous Improvement in Warehouse Quality System. Responsible for monitoring inventories and non-moving scrap salvaging. Carrying out inventory / warehouse management of raw materials; replenishing stock items by raising purchase indents/ delivery advices and scrutinizing purchase indents. Governing the inventory function so as to curtail inventory-holding expenses and adherence to the minimum inventory level to minimize wastage. Conduct cGMP training and evaluation to warehouse Staff & Identify HSE training needs for awareness and Competence. Developing Training Modules for Different Levels in WH. Verifying the Daily usage log books and monitoring the daily procedures as per SOP. Identification of Risks & Hazard, Environmental aspects & evaluation and review the same. Providing various MIS Analysis related to WH/inventory trend analysis to management on monthly basis. Key Competencies (Technical, Functional & Behavioral) Technical & Functional: Good communication skills Demonstrate ownership and collaboration at work Primary Responsibilities: Overall Responsible for all the activities of the Warehouse department beside day –to- day activities Like Material Receipt, Issues, Distribution of Finished goods, Record/Documentation as per the

JOB RESPONSIBILITIES: Overall Responsible for all the activities of the Warehouse department beside day –to- day activities Like Material Receipt, Issues, Distribution of Finished goods, Record/Documentation as per the C GMP Procedure as well as EOU statutory compliance. Responsible for upkeep of the quality system as per the c GMP in Ware house. Responsible For Continuous Improvement in Warehouse Quality System. Responsible for monitoring inventories and non-moving scrap salvaging. Carrying out inventory / warehouse management of raw materials; replenishing stock items by raising purchase indents/ delivery advices and scrutinizing purchase indents. Governing the inventory function so as to curtail inventory-holding expenses and adherence to the minimum inventory level to minimize wastage. Conduct cGMP training and evaluation to warehouse Staff & Identify HSE training needs for awareness and Competence. Developing Training Modules for Different Levels in WH. Verifying the Daily usage log books and monitoring the daily procedures as per SOP. Identification of Risks & Hazard, Environmental aspects & evaluation and review the same. Providing various MIS Analysis related to WH/inventory trend analysis to management on monthly basis. Key Competencies (Technical, Functional & Behavioral) Technical & Functional: Good communication skills Demonstrate ownership and collaboration at work Primary Responsibilities: Overall Responsible for all the activities of the Warehouse department beside day –to- day activities Like Material Receipt, Issues, Distribution of Finished goods, Record/Documentation as per the

Role: Documentation Department: Production Location: Bidar About Us: Sai Life Sciences is one of the fastest-growing Contract Research, Development, and Manufacturing Organizations (CRDMOs). As a pure-play, full-service partner, we collaborate with over 300 global innovator pharma and biotech companies to accelerate the discovery, development, and commercialization of their NCE programs. We have over 3000 employees across our facilities in India, the UK, and the USA, working together to deliver scientific excellence and customer success. We are a Great Place to Work certified organization with a culture of openness, mutual respect, and inclusivity. We embrace diversity and follow equal opportunity practices across all levels. Key Responsibilities : Drafting and Review of Investigation Reports in co-ordination with cross functional departments like Production Blocks, Maintenance, Process Engineering, QA, CQA, PR&D, QC and AR&D etc. Preparation of Quality Risk Assessment and its Impact Assessment Reports as or when required. Handling of documents related to Quality Management System (QMS) like Change controls, Deviations, Planned changes, CAPAs etc., as per requirement in co-ordination with cross functional departments like Production Blocks, Maintenance, Process Engineering, QA, CQA, PR&D, QC, AR&D etc. Follow the cGMP compliance by following the SOPs and approved procedures. Responsible for any activities assigned by HOD or Senior Management. Experience/Qualification: M.Sc/B.Tech/Diploma (Chemistry/Chemiscal) with 4-9 years of relevant industry experience. Key Competencies (Technical, Functional & Behavioural): 1. Must have GMP requirement and QMS knowledge. 2. Excellent written communication, interpersonal skills, data analysis and understanding of business processes.

Key Responsibilities To ensure that appropriate personal protective equipment’s in the laboratory premises and follows the safety precautions. Ensure the good organization and housekeeping of the PRD department work area. Execute the developmental synthesis of the NCEs / API intermediate / target molecules. Excel in the observation, recordings and reporting skill sets for the scientific data. Prior to designing laboratory experiments, the MSDS of all input materials shall be obtained and scrutinized for risk assessment. Work as a team and take responsibility with accountability. Surveys the literature for information concerning specific compounds. Experimental data related to process development studies of the NCEs / API intermediate / target molecules manufacturing shall be recorded in Electronic Note Book (ELN).

JOB RESPONSIBILITIES: To maintain warehouse operation in accordance with cGMP procedures & ensure smooth operation in warehouse department. Responsible for raw material Issues and document updating of on-line log book activity and GMP pro. Monitoring the day-to-day activities related to warehouse. Responsible for recording the daily usage logbooks. To ensure that the warehouse related SOP’s are being followed. To ensure that avoid the cross contamination and proper storage of the material. To responsible to check the issuance of the material to production as per FIFO/FEFO. To responsible to monitor the materials due for re-testing and intimation to QC for sampling and testing purpose. To ensure all statutory and regulatory requirements complied in respect of customer and regulatory requirement. To monitor the updating of status boards. To receive the intermediates from respective production blocks and check the weights and labelling part. To be responsible to post the daily consumption/issues RM/PM in GMP pro and generation of stock reports on day to day basis reconciliation accuracy. Supervision of Environmental monitoring in respective storage areas. Monthly Physical Verification of Stock for Materials. Key Competencies (Technical, Functional & Behavioural) Technical & Functional: Good communication skills Demonstrate ownership and collaboration at work Primary Responsibilities: To maintain warehouse operation in accordance with cGMP procedures & ensure smooth operation in warehouse department.

Summary of Job : To handle Analytical activities for the R&D campus. Key Responsibilities To be aware of the project scope and finer aspects of scope as well as scope changes. To plan and conduct the analysis with required skills. To develop the suitable methods based on the scope of analysis. To guide analysts, in the following aspects Analytical method development approach oAnalysis planning oGeneration of required data oAnalytical requirements oDrawing inference from the analytical results oSafety and GMP / GLP compliance. oResponsible for oCompiling data oPreparing Analytical Technical reports etc. oPrepare weekly project updates oPreparing AMD Reports oInteraction with PE, PM and PR&D teams oCustomer communications and participate in customer telecoms oPreparing tech transfer documents Expected to highlight the potential road blocks / issue to the Team lead. Ensuring to maintain the analytical requirements specific to projects (reagents, columns, etc.) Key Competencies (Technical, Functional & Behavioral) May or may not be the project lead to the customer. May or may not or partially - need based works with his own hands. Primary Responsibilities: To handle Analytical activities for the R&D campus.