Oversee the complete Procure-to-Pay (P2P) cycle for all MRO (Maintenance, Repair & Operations), Engineering Services, IT Procurement, Admin , Fuel, Energy & & Services, Ensure effective implementation of Sourcing and Procurement SOPs related to all Indirect Materials and Services. Drive the adoption of best practices in Supply Chain Management (SCM) to enhance efficiency and cost-effectiveness. Ensure 100% compliance with SAI Quality Management Systems, statutory requirements, and regulatory guidelines. Establish and maintain systems for periodic reviews with cross-functional teams to ensure alignment and improvement. Prepare and circulate detailed Monthly MIS Reports on purchases and procurement activities to key stakeholders. Maintain healthy supplier relationships, and ensure timely resolution of vendor issues and disputes. Lead the development and capability building of team members; create and implement individual success plans for key activities. Manage and prioritize the vendor payment plan to support uninterrupted business operations. Conduct regular reviews with internal stakeholders to identify, understand, and resolve procurement-related issues. Ensure timely PR (Purchase Requisition) to PO (Purchase Order) conversion in line with agreed SLAs. Provide strong team leadership, performance management, and foster a high-performance work culture. Identify opportunities for cost optimization, process improvements, and supplier consolidation. Drive digital transformation initiatives in procurement (e.g., e-procurement, ERP upgrades). Conduct vendor assessments and audits to ensure quality, compliance, and performance standards. Collaborate with Finance and Legal teams for contract finalization and risk mitigation. Support internal and external audits and ensure timely closure of audit findings. Contribute to strategic sourcing initiatives and long-term procurement planning. Coordinate with the Finance team for timely processing of vendor payments and alignment of procurement budgets. Partner with the Engineering team to source and procure technically complex materials and services efficiently. Show more Show less

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. Show more Show less

Role: Associate - Transporters and hepatocytes research (DMPK) Department: DMPK 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. Key Responsibilities : Hands-on experience in conducting transporter uptake and inhibition assays using HEK293 stably transfected cell lines. Prior experience in validation of transporter transfected cell lines and support the customers with customised assay conditions. Experience in conducting the oil spin method for assessing uptake and inhibition. Hands-on experience or ability to conduct CYP450 inhibition studies using hepatocytes. Experience in conducting in vitro transporter assays with radioisotope labelled compounds. Maintenance of cell line inventory and lab infrastructure. Support IND-enabling studies, routine screening, and generate high-quality data. Participation in scientific innovation projects in the field of drug transporters. Familiarity with the extended clearance classification system. Knowledge of data compilation and interpretation for test compound classification systems, either as substrates or uptake inhibitors. Ability to understand and read data, identify data variability, and participate in data review cycles with the QA team. Commitment to delivering data within agreed timelines (< 7 days) and strong work ethics to complete assigned tasks. Excellent communication and collaboration skills, working closely with team members. Good oral and written communication skills. Education and Experience: M Pharm (Pharmacology/Pharmaceutics) with 3-8 years of experience or MSc with 6-8+ years of experience in DMPK of small molecule drug discovery and development, preferably in a CRO or Biotech/Pharma industry. Knowledge of FDA and EMA industry guidance. Show more Show less

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 Show more Show less

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. Show more Show less

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): Must have GMP requirement and QMS knowledge. Excellent written communication, interpersonal skills, data analysis and understanding of business processes. Show more Show less

Role: System Administrator Department: IT 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 : IT assignments as assigned by Reporting Manager, Corporate ITS and plant HOD’s. Handling of all GxP Servers at site connected at such as Empower, ICDAS, Historian, Server SlslLab, AD server. Maintaining Data centre activities such as ensuring temperature recording, humidity, pest control, man movements, and safety-related activities. Act as System Administrators in Operating System and Instrument/Equipment (GxP) connected application software, Troubleshooting, and Data backup/restore management. Identifying the data from instrument/equipment connected application software in Lab and Manufacturing areas schedule their backups in backup solution software and maintain the list as per SOP requirements. Performing/Monitoring the data backup as per schedule or manually and maintain the backup media and activities logs as per SOP requirements. Performing the data restore on user’s requests/ periodically, verify it along with users and maintain their activities logs in line to SOP requirements. Performing and maintaining the activities logs logging the applications administration activities such as System Configuration & Security Policies Implementing, Privileges & Roles Management, User Management - User Creation, Modification, Enable/Disable, Lock/Unlock etc.) as per SOP for the Lab and Manufacturing systems Implementing the required security patches at OS level on instruments/equipment’s connected GRP computer systems in Lab and Manufacturing Verification and correction of date & time on Lab and Manufacturing instruments and standalone GxP computer systems. Performing the changes in instruments/equipment connected applications software in Lab and Manufacturing areas as per change management procedure. Completing/implementing the sites IT related Change Controls, Deviations, Investigation Reports, CAPAs, and Audit Observations if any. Execution/Review of computer systems qualification and validation (CSV) activities in Lab and Manufacturing areas systems as per Computer Systems Validation requirements. Facing the internal/regulatory audits and able to demonstrate the required compliance & controls are in place w.r.t. IT systems administrations, Operations, data backup/restore, security, traceability and integrity to the auditors on demand. Implementing the required new/revised SOPs at sites and ensuring the overall compliance of the same. Liaison with IT Infra team and vendors for technical support/escalations w.r.t. Operating Systems (OS), instrument/equipment connected application software, data backups & restore. Experience/Qualification: B.Tech/MCA with 4-6 years of relevant industry experience. Key Competencies (Technical, Functional & Behavioural): Good communication skills Demonstrate ownership and collaboration at work Show more Show less

Role: Project Manager - (API-CRDMO) Department: Project Management 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. Key Responsibilities: Responsible for timely kick off the awarded project. Responsible to prepare and update, comprehensive Gantt chart for the project delivery schedule. Driving end to end PM activities, maintain schedules and project budgets. Regularly coordinate with CFT comprising of PR&D, AR&D, PE, QA, QC, Production etc, through daily meetings as well as issue based meetings. Prepare and update the comprehensive action tracker for the project activities. Organize the interactions with customer and facilitate discussion between technical teams Present the project status in the Project Review Meetings with Central Delivery Review Team (CDRT) Highlight and escalate the road blocks or anticipated road blocks to the senior management team. Ensure complete and timely documentation on project closure Timely raise the invoice and update finance and BD of the same. Performance Indicators QUOTIF as per commitment Overall management of projects, project creeps and communication Job specifications / pre-requisites: (Qualification, experience, any other specifications) M.Sc. (Chemistry) or Chemical Engineering, with minimum 12 years’ experience working along with CFTs (PR&D, AR&D, Technology Transfer, Process Engineering, Production or Outsourcing) PMP certification and or MBA desired, but not must. Additionally, minimum 4 years’ experience as Program Manager with a reputed CDMO. Ideally API CDMO but can also be from formulation CDMO or least preferred from Clinical Research Organization. Key Competencies (Technical, Functional & Behavioural) - Excellent verbal and written communication, persuasiveness, inter-personal skills, adaptability, foresight, understanding of business processes. Show more Show less

Department Quality Assurance (Medchem) Position Executive / Sr. Executive Reports to Team Lead Location Shameerpet, Hyderabad Key Responsibilities: Issue, review the R&D LNBs and ELN Check the compliance of observations found during review. Archiving of LNBs. Scanning of LNBs. Dispatch of LNBs & data as per client request. Conduct Lab audits and re-inspection as and when required. Training to new joiners for LNB writing, data integrity, good documentation practices as and when required Qualification M.Sc. Organic chemistry/ M.Pharm – Medicinal chemistry /Analytical Chemistry Key Competencies (Technical, Functional & Behavioural) Excellent verbal and written communication Persuasiveness Inter-personal skills Adaptability Foresight Understanding of business processes.

Initiation, review and approval of all types of quality management systems (Ex: Change controls, Deviations, Investigations, CAPA, OOS, and Complaints etc. Handling of Return Goods. Handling of quality system and perform risk assessment to the required quality system. Conduct regular internal audits as per the need basis. Reviewing and approving of all documents (SOP’s, Spec & STPs, Forms, protocols and reports etc.) Review of annual product quality review reports. Providing training on all cGMP topics to employees at site. Supporting to customer audits/ visits and regulatory audits. Support to provide necessary documents for amendments, annual updates and regulatory filings and CMC supporting documentation. Filling of questionnaires, declarations & quality agreements. Execution of additional responsibilities assigned by HOD

Role: Project Manager - (API-CRDMO) Department: Project Management 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. Key Responsibilities: Responsible for timely kick off the awarded project. Responsible to prepare and update, comprehensive Gantt chart for the project delivery schedule. Driving end to end PM activities, maintain schedules and project budgets. Regularly coordinate with CFT comprising of PR&D, AR&D, PE, QA, QC, Production etc, through daily meetings as well as issue based meetings. Prepare and update the comprehensive action tracker for the project activities. Organize the interactions with customer and facilitate discussion between technical teams Present the project status in the Project Review Meetings with Central Delivery Review Team (CDRT) Highlight and escalate the road blocks or anticipated road blocks to the senior management team. Ensure complete and timely documentation on project closure Timely raise the invoice and update finance and BD of the same. Performance Indicators QUOTIF as per commitment Overall management of projects, project creeps and communication Job specifications / pre-requisites: (Qualification, experience, any other specifications) M.Sc. (Chemistry) or Chemical Engineering, with minimum 12 years’ experience working along with CFTs (PR&D, AR&D, Technology Transfer, Process Engineering, Production or Outsourcing) PMP certification and or MBA desired, but not must. Additionally, minimum 4 years’ experience as Program Manager with a reputed CDMO. Ideally API CDMO but can also be from formulation CDMO or least preferred from Clinical Research Organization. Key Competencies (Technical, Functional & Behavioural) - Excellent verbal and written communication, persuasiveness, inter-personal skills, adaptability, foresight, understanding of business processes.

As a Project Manager at Sai Life Sciences, a leading Contract Research, Development, and Manufacturing Organization (CRDMO), you will play a crucial role in overseeing the successful delivery of projects within the API-CRDMO department based in Hyderabad. Your responsibilities will include: - Ensuring timely kick-off of awarded projects and preparing comprehensive Gantt charts for project delivery schedules. - Managing end-to-end project management activities, including maintaining schedules and project budgets. - Coordinating regularly with Cross-Functional Teams (CFT) such as PR&D, AR&D, PE, QA, QC, and Production through meetings to address project-related issues. - Updating and maintaining a detailed action tracker for project activities. - Facilitating interactions with customers and coordinating discussions between technical teams. - Presenting project status in Project Review Meetings with the Central Delivery Review Team (CDRT). - Identifying and escalating any roadblocks or anticipated challenges to senior management. - Ensuring thorough and timely documentation for project closure. - Timely raising of invoices and updating finance and business development teams accordingly. To excel in this role, you should possess the following qualifications and experience: - A degree in M.Sc. (Chemistry) or Chemical Engineering with a minimum of 12 years of experience working with Cross-Functional Teams (PR&D, AR&D, Technology Transfer, Process Engineering, Production, or Outsourcing). - PMP certification and/or an MBA would be desirable but not mandatory. - At least 4 years of experience as a Program Manager with a reputable CDMO. - Ideally, experience in API CDMO, although candidates from formulation CDMO or Clinical Research Organization backgrounds will also be considered. Key competencies required for this role include excellent verbal and written communication skills, persuasiveness, strong interpersonal skills, adaptability, foresight, and a good understanding of business processes. If you are looking for a challenging role in project management within the pharmaceutical industry and have a passion for driving successful project outcomes, we encourage you to apply for this exciting opportunity at Sai Life Sciences.,

You will be responsible for initiating, reviewing, and approving various quality management systems such as Change Controls, Deviations, Investigations, CAPA, OOS, and Complaints. In addition, you will handle Return Goods and ensure the proper functioning of the quality system by performing risk assessments as needed. Conducting regular internal audits will also be part of your duties. Reviewing and approving all documents including SOPs, Spec & STPs, Forms, protocols, and reports will be crucial to ensure compliance. You will also review annual product quality review reports and provide training on cGMP topics to employees at the site. Additionally, you will support customer audits/visits and regulatory audits, as well as provide necessary documentation for amendments, annual updates, regulatory filings, and CMC supporting documentation. Your role will also involve filling out questionnaires, declarations, and quality agreements. Finally, you will execute any additional responsibilities assigned by the Head of Department.,

As a Project Manager at Sai Life Sciences, a leading Contract Research, Development, and Manufacturing Organization (CRDMO), you will play a crucial role in accelerating the discovery, development, and commercialization of NCE programs for over 300 global innovator pharma and biotech companies. With a workforce of more than 3000 employees spread across our facilities in India, the UK, and the USA, we are committed to delivering scientific excellence and ensuring customer success. Embracing diversity and equal opportunity practices, we foster a culture of openness, mutual respect, and inclusivity. Your primary responsibilities will include ensuring the timely kick-off of awarded projects, preparing and updating comprehensive Gantt charts for project delivery schedules, and driving end-to-end project management activities while maintaining schedules and project budgets. You will collaborate closely with cross-functional teams comprising of PR&D, AR&D, PE, QA, QC, and Production through regular meetings to coordinate project activities effectively. Additionally, you will be responsible for organizing interactions with customers, facilitating discussions between technical teams, and presenting project status in Project Review Meetings with the Central Delivery Review Team (CDRT). Identifying and escalating roadblocks or anticipated challenges to the senior management team, ensuring complete and timely project documentation, raising invoices promptly, and updating finance and business development teams are also crucial aspects of your role. To excel in this position, you should hold an M.Sc. in Chemistry or Chemical Engineering with a minimum of 12 years of experience working alongside cross-functional teams. While a PMP certification and/or MBA are desired, they are not mandatory. Having at least 4 years of experience as a Program Manager in a reputable CDMO is essential. Ideally, you should have experience in API CDMO, with formulation CDMO as a secondary preference, and clinical research organization experience being the least preferred. Key competencies required for this role include excellent verbal and written communication skills, persuasiveness, strong interpersonal skills, adaptability, foresight, and a deep understanding of business processes. Join us at Sai Life Sciences and be part of a dynamic team dedicated to driving innovation and success in the pharmaceutical and biotech industries.,

You will be responsible for initiating, reviewing, and approving various quality management systems such as Change Controls, Deviations, Investigations, CAPA, OOS, and Complaints. You will also handle Return Goods and ensure the smooth functioning of the quality system by performing risk assessments as required. Conducting regular internal audits and reviewing/approving all documents including SOPs, Spec & STPs, Forms, protocols, and reports will be part of your duties. Additionally, you will review annual product quality review reports, provide training on cGMP topics to employees, and support customer audits/visits as well as regulatory audits. You will assist in providing necessary documents for amendments, annual updates, regulatory filings, and CMC supporting documentation. Other tasks may include filling out questionnaires, declarations, quality agreements, and executing any additional responsibilities assigned by the Head of Department.,