Education : M.Sc / PhD Experience: 8 to 15 years Job responsibilities Design and perform multi-step syntheses of novel ADC payloads, key intermediates. Develop and optimize synthetic routes for early-stage drug projects. Analyse and record data using Electronic Laboratory Notebooks. Handle analytical instruments including HPLC, LC/MS and NMR for structural determination and purity assessment. Requirements Deep understanding of organic functional groups, reaction mechanisms, and reactivity. experience in multi-step synthesis, purification, and characterization of organic compounds. Familiar with NMR and mass spectroscopy. Strong interpersonal skills and effective written/verbal communication

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 : 1. IT assignments as assigned by Reporting Manager, Corporate ITS and plant HODs. 2. Handling of all GxP Servers at site connected at such as Empower, ICDAS, Historian, Server SlslLab, AD server. 3. Maintaining Data centre activities such as ensuring temperature recording, humidity, pest control, man movements, and safety-related activities. 4. Act as System Administrators in Operating System and Instrument/Equipment (GxP) connected application software, Troubleshooting, and Data backup/restore management. 5. 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. 6. Performing/Monitoring the data backup as per schedule or manually and maintain the backup media and activities logs as per SOP requirements. 7. Performing the data restore on user’s requests/ periodically, verify it along with users and maintain their activities logs in line to SOP requirements. 8. Performing and maintaining the activities logs logging the applications administration activities such as System Configuration & Security Policies 9. Implementing, Privileges & Roles Management, User Management - User Creation, Modification, Enable/Disable, Lock/Unlock etc.) as per SOP for the Lab and Manufacturing systems 10. Implementing the required security patches at OS level on instruments/equipment’s connected GRP computer systems in Lab and Manufacturing 11. Verification and correction of date & time on Lab and Manufacturing instruments and standalone GxP computer systems. 12. Performing the changes in instruments/equipment connected applications software in Lab and Manufacturing areas as per change management procedure. 13. Completing/implementing the sites IT related Change Controls, Deviations, Investigation Reports, CAPAs, and Audit Observations if any. 14. Execution/Review of computer systems qualification and validation (CSV) activities in Lab and Manufacturing areas systems as per Computer Systems Validation requirements. 15. 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. 16. Implementing the required new/revised SOPs at sites and ensuring the overall compliance of the same. 17. 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 4-9 years of relevant industry experience. Key Competencies (Technical, Functional & Behavioural): 1. Good communication skills 2. Demonstrate ownership and collaboration at work

Department: Formulations Location: Shameerpet 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 : 1. Hands on experience in developing and manufacturing oral solid dosage form and enabling/novel formulations for improving the oral bioavailability of new chemical entity (NCE). 2. Hands on experience in physicochemical characterization, solid state characterization, and solid form screening 3. In depth knowledge about physicochemical properties of NCEs that govern developability of drug candidates. 4. Hands on experience in preparation of protocols, guidelines and SOPs for lab equipments/instruments and processes. 5. Should have good understanding about the principles of GLP, GMP and ICH guidelines. 6. Should understand systems and process pertaining to safety, health and environment. Experience/Qualification: M. Pharm with 2-4 years of relevant industry experience. Key Competencies (Technical, Functional & Behavioral): 1. Good communication skills 2. Should possess good team management 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/Chemical) with 4-9 years of relevant industry experience. Key Competencies (Technical, Functional & Behavioral): 1. Must have GMP requirement and QMS knowledge. 2. Excellent written communication, interpersonal skills, data analysis and understanding of business processes.

1. Revision of HSE SOPs, guidelines and formats. 2. Preparation of new HSE SOPs and guidelines. 3. Raise, follow up and closure of document change controls and initiation of procedures. 4. Compilation and rolling out of the HSE & Sustainability MIS report on organization scale. 5. Implement HSE& Sustainability management systems at sites. 6. Guide sites on the initiatives taken in HSE for implementation. 7. Harmonization of systems and practices across the sites. 8. Governance of Process Map- HSE digital platform for data hygiene and update by the sites. 9. Build capability to the sites on the required topics like incident investigation, process map usage, etc. 10. Lead HSE & Sustainability digital initiatives and collaborate with IT team for successful implementation 11. Lead HSE related events like National Safety Day, Environment Day activities etc. 12. Raise Purchase Requests for HSE department and follow up for closure of the purchases. 13. Coordinate for HSE & Sustainability awards application, site assessment and document collection and verification. 14. Conduct Industrial Hygiene governance calls to monitor progress on the exposure assessments and related activities 15. Excellent communication, collaboration, and analytical skills

Internal Communications Develop and implement an integrated internal communications strategy to inform, inspire, and connect employees across locations. Curate and manage communications across platforms intranet, emails, newsletters, digital signage, town halls, etc. Partner with business and functional teams to communicate key priorities, initiatives, policies, and leadership messages. Manage end-to-end content development – from ideation to delivery – including written, visual, and multimedia formats. Track employee engagement metrics and continuously improve communication approaches based on feedback. Support change communication for key organizational initiatives (digital transformation, culture, etc.). Corporate Social Responsibility (CSR) Collaborate with senior leadership to shape the company’s CSR strategy and annual plans, including in-house programs and partnerships with credible NGOs. Conceptualize, design, and execute impactful CSR projects aligned with organizational goals, ensuring timely delivery and measurable outcomes. Design and lead employee engagement initiatives that foster direct interaction with beneficiaries, offering meaningful volunteer experiences that uplift communities and enhance employee fulfilment. Drive communication around CSR initiatives, including internal updates, impact storytelling, milestone celebrations, and external visibility through social media and reporting. Build and manage relationships with external partners, facilitate audits, and ensure compliance and transparency across all CSR activities. Desired Skills & Qualifications * Postgraduate degree in Communications, Marketing, Social Work, or a related field. * 5-8 years of relevant experience in internal communications and/or CSR roles, preferably in a corporate setting. * Exceptional writing, editing, and storytelling skills. * Proficiency in digital communication tools and platforms (MS Office, SharePoint, graphic/AV tools is a plus). * Strong project management, interpersonal, and stakeholder engagement skills. * Passion for employee engagement and social impact.

Role: Veterinary Pathologist Department: DMPK and Toxicology 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 : Manage all activities related to necropsy, clinical pathology and histopathology. Health monitoring of laboratory animals Histopathology slide evaluation Maintenance of activities in animal house Study personnel and /or Study Veterinarian in Toxicology studies Assistance in invitro and genetic toxicology studies Experience in maintenance of all equipment in clinical and histopathology. Experience in audits from external agencies like CPCSEA, AAALAC, etc. Education and experience: M. V. Sc. in Pathology/IBTP Board Certification is highly plus. 3+ years experience in toxicology small molecule drug development preferably in CRO or in Biotech/Pharma industry. Knowledge in animal house activities, toxicology and toxicologic pathology Good oral/written communication skills.

Department: PPIC 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 Efficient Production Planning & Schedules to ensure a smooth manufacturing process & meeting customer committed date and OTIF. Applying Lean Inventory Management & Forecast the inventory for key project based on the historical data & future assumption. Excellent knowledge of production planning and quality controls principles. Scheduling production batches based on raw material level in the inventory and production time. Monitoring and coordination with supply chain team based on storage space at warehouse and day to day changes in production plan. Optimum resource utilization in an environment of multi plant / multi location and multi facets of varied equipment set up. Continual improvement in equipment utilization of equipment with aim of No Overuse or Underuse. Experience/Qualification: M.Tech/MBA/M.Sc/B.Tech with 8-13 years of relevant industry experience. Key Competencies (Technical, Functional & Behavioral): Excellent work knowledge in Microsoft Excel is must with all functionalities. MIS Report Daily/Weekly/Monthly as per need. Database Management for PPIC function.

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.

Key Responsibilities To timely kick off the awarded project To timely prepare and update, comprehensive Gantt chart for the project delivery schedule Regularly coordinate with CFT comprising of PR&D, AR&D, PE, QA, QC, Production etc, through daily meetings as well as issue based meetings To prepare and update the comprehensive action tracker for the project activities To send the prescheduled updates to the customer and BD To schedule the telcons / VC with customer and facilitate discussion between technical teams To highlight and escalate the road blocks or anticipated road blocks to the senior management team To ensure complete and timely documentation on project closure To 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 communications 2. Job specifications / pre-requisites: (Qualification, experience, any other specifications) M.Sc. (Chemistry) or Chemical Engineering, with minimum 6 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. Qualification Masters/ Bachelors (preferred PMP certified , not Mandatory) Experience 15 to 20 Yrs Key Competencies (Technical, Functional & Behavioral) - Excellent verbal and written communication, persuasiveness, inter-personal skills, adaptability, foresight, understanding of business processes.

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

Role: Veterinary Pathologist Department: DMPK and Toxicology 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. Job Summary: We seek a Toxicologic Pathologist with expertise in toxicology study design, oversight, and histopathology evaluation. This role involves toxicologic and pathology assessments, supporting drug development. Key Responsibilities : Manage pathology functions at Sai Life Sciences. Conduct gross and microscopic evaluations of tissues from rodent studies (acute, subchronic). Diagnose and interpret neoplastic and non-neoplastic lesions (following INHAND terminology). Integrate histopathology findings with clinical pathology, organ weights, and in-life observations. Serve as Study Pathologist for nonGLP toxicology studies. Author and review pathology reports, NOAEL/LOAEL assessments, and risk summaries. Mentor junior pathologists and toxicologists. Qualifications: Required MVSc or PhD in veterinary Pathology. 7-12 years of experience in pharma/CRO toxicology studies. Expertise in rodent/non-rodent pathology using H&E, special stains, and IHC. Strong knowledge of GLP, OECD, and ICH S1-S11 guidelines. Preferred Experience with biologics, oncology, or genetic toxicology. Proficiency in digital pathology.

Job Responsibilities: Develop interior layouts for lab drawer systems and integrated storage using space optimization principles, zonal mapping, and workflow simulations. Review scientist working, understand technical detailing and design Fume Hood & its Drawers factoring in clearance zones, airflow considerations, and user movement analysis. Understand lab inventory and design the custom-fit insert/organizers along with ergonomics & 6S. Design custom-fit inserts and organization systems for cold storage equipment (refrigerators/freezers) to support temperature-sensitive categorization and minimize material handling time. Maximize horizontal and vertical space efficiency through multi-level shelving, pull-out systems, and built-in cabinetry tailored to lab operations. Generate design plans and detailed drawings using AutoCAD, Revit, or SketchUp. Work cross-functionally with lab managers, engineers, and fabrication teams to translate requirements into workable solutions. Qualification Bachelors or masters in interior design Experience Fresher Key Competencies (Technical, Functional & Behavioral) Technical & Functional Behavioral: Currently pursuing or completed a degree in Interior Design, Architecture, or related field. Proficient in AutoCAD, SketchUp, Revit, or equivalent BIM tools. Knowledge of lab planning guidelines, ergonomic codes, and storage optimization strategies. Strong design documentation and presentation skills (rendering, mood boards, concept sketches). Detail-oriented with a focus on form-to-function alignment in technical spaces

Role: Chemist / Sr Chemist 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. Summary of Job: To execute the production through the various stages of manufacturing as per the plan and ensure compliance to quality, safety & regulatory requirements. Key Responsibilities : Execute production batches as per plan. Preparation of SOPs. To maintain the yield of products in specifies limits at various stages of process activities. Online verification of cleaning area / equipment and completion of Logs. Online monitoring of environment conditions and completion of Logs. To comply with cGMP standard during the entire process activity. Manufacturing of products as per cGMP. Online completion of batch process records. To maintain the process facility as per the regulatory norms. Experience/Qualification: M.Sc/ B.Sc/ B.Tech/ Diploma (Chemistry/Chemical) with 2-8 years of relevant industry experience. Key Competencies (Technical, Functional & Behavioural): Sound knowledge on theoretic aspects of Chemical Engineering Basic knowledge of API process and handling production machinery of manufacturing. Good interpersonal Skills

JOB RESPONSIBILITIES: To monitor and coordinate all Projects Civil request are closed and documented including New Projects as per SAI procedures. Responsible for day to day site Civil works like Masonry, carpentry, plumbing works, clean Room painting and flooring, clean room partitions, exterior works, non-clean room interior Works and plumbing works. Execute civil projects as per scope & specifications, monitor quality check during Construction and certify quantities as per site measurement. Providing cost estimations, comparisons for various types of civil works. Attend training sessions on cGMP, SAI procedures/policies, Regulatory, latest Technical & Industrial developments related to engineering. Support to Projects in terms of civil, structural fabrication and erection related works i.e Designing, Planning, BOQ verification, execution and bill verification. To coordinate inter departmental team i.e. civil, electrical, mechanical and instrumentation and support to perform identified task in compliance with GMP standards. To approve specifications for engineering consumables to be procured. Monitoring inventory of spares in store and ordering for require spares. To enforce the Safety rules and regulations in plant.

Key Responsibilities To Lead and drive Instrumentation and automation maintenance for the entire facility Preparation of Basic and Detailed Engineering for Instrumentation and PLC Automation Projects. Planning, Installation, Pre-Commissioning, Commissioning and Qualification of Instrumentation and PLC Automation Projects. To ensure Daily Calibration of Instruments as per the Schedule. To ensure Uninterrupted running of Process and Utility Equipment's. To ensure minimize the Breakdown Time of Plant Equipment / Instrument Systems. Analyze and resolve work related problems or assist the team/technicians in resolving the issues. To do modification works as per the approved change control. Involving in all Qualifications as part of Instrumentation Scope. Responsible for Preparing & Training on SOPs related to Instrumentation. To support the documentation related to Change Controls, Deviations, Investigations and CAPAs etc. to comply as per the CGMP guidelines, Site Quality Procedures and GQDs. Responsible for Audit Compliances. Responsible to participate in Quality Risk Management & Quantitative Risk Analysis exercises. Responsible to build up a good working relation with Cross Functional & Inter Departmental Teams. To impart training to the team to perform their duties as per CGMP and GDP. Ensure effective work processes and procedure are in place and are being followed / used by all the team members. To coordinate with external agencies and contractors for day to day work. Responsible for keeping the areas and documents ready for various Regulatory Inspections / Audits and need based active participation during audits. Responsible for establishing & maintaining systems for spares as part of Instrumentation in process & utilities Equipment’s and its budget requirement. To coordinate with purchase department and Engineering store for spare parts. Maintain awareness on HSE requirements and implementation of the same as per the group policies, rules & regulations. To carry out the activities assigned by the Head of Engineering department from time to time. Technical & Functional: Good communication skills Demonstrate ownership and collaboration at work People Manager

Role: Support and assist in Talent Acquisition process Assist in creating process flows, hiring metrics pertaining to TA. Learn and contribute to projects / initiatives in Talent Acquisition. Actively participate in Walk-in / Virtual Recruitment Drives. Incumbent should posses: Effective communication skills Moderate to advanced MS office skills Self starter.