Preferred Qualification: M.Sc Organic Chemistry with more than 70% aggregate Looking for freshers who can join immediately Roles & Responsibilities: Synthesize, and characterize novel bioactive molecules under supervision of scientist/senior scientist Knowledge of modern organic chemistry and synthetic methods: heterocyclic chemistry, metal catalysed reactions, multi-step synthesis. Knowledge of techniques in synthesis, purification, and spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, etc.). Maintain Lab note book. Understanding of systems and process pertaining to safety, health and environment.

Preferred Qualification: M.Sc Organic Chemistry with more than 70% aggregate Looking for freshers who can join immediately Roles & Responsibilities: Synthesize, and characterize novel bioactive molecules under supervision of scientist/senior scientist Knowledge of modern organic chemistry and synthetic methods: heterocyclic chemistry, metal catalysed reactions, multi-step synthesis. Knowledge of techniques in synthesis, purification, and spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, etc.). Maintain Lab note book. Understanding of systems and process pertaining to safety, health and environment. LAST DATE for application: 14th May 2025. Selection Process: Candidates who have applied shall be shortlisted based on their academic marks. Technical test and aptitude test will be conducted online on 15th May 2025. Interviews will be scheduled on 17th May 2025 for the shortlisted candidates at Aurigene Oncology Ltd, Bangalore.

Preferred candidate profile: PhD (Organic chemistry / Medicinal chemistry) with 5 -6 years of experience in antibody drug conjugates (ADC) development Roles & Responsibilities: Must have hands on experience in linker- payload synthesis and overall understanding of ADC. Should be able to design and execute synthesis of complex drug linkers and ADC payloads. Should have proficiency in characterization and analysis of synthesized molecules using analytical techniques such as HPLC, LC-MS and NMR. Thorough understanding of linker chemistry and latest development in the space. Efficient employment of structure-based drug design principles and integrate with other experimental data collected in the design of new linkers. Mentor and manage team members for high performance and scientific growth. Collaborate with project team members and communicate progress against goals in a multidisciplinary setting: chemistry, antibody engineering, biology, pharmacology, DMPK, and external collaborators. Accurate documentation of experiment and maintaining a well-organized laboratory notebook (LNB). Understanding of systems and process related to safety, health, and environment (SHE).

Desired Profile: DMLT/ B.Sc. in Medicsl Lab Technology/life sciences with 3 - 6 years of experience in Necropsy, tissue collection, preservation, tissue processing, tissue embedding and slide preparation. Role & responsibilities: Responsible for performing necropsies for preclinical safety and pharmacology studies in different strains, activities include collection of blood, bone marrow smear preparation, organ collection, weighing and preservation as per the study protocol requirement. Responsible for bone marrow smear preparation at the time of necropsy. Responsible for tissue QC and tissue preservation. Preparation of Histopathology slides for the microscopic evaluation includes some of the techniques like, fixation, trimming of fixed tissues, processing of tissues and staining and labelling of the slides before submitting for HP evaluation. Responsible for preparation of all the reagents and buffer: Buffers like NBF, MDF, DF, Decalcifying fluid, etc. Performing special stains like PAS. Responsible for stock stain preparation: Hematoxylin, Eosin, May-Grunewald, Giemsa stain, Schiff reagent and periodic acid. Quality check of stained slides. Prepare, peer review and revision of SOPs pertaining to department. Archiving of study samples (tissue blocks and tissue slides). Understanding of systems and process pertaining to safety, health, and environment. Operation and usage of relevant equipment used in non-clinical safety studies like biological centrifuge, laminar air flow, anesthetic machine, weighing balances, refrigerator, deep freezers, tissue Stainer, tissue processor, microtome, tissue floatation bath, tissue embedding station, etc. Preparation and review of SOPs. Archival of the study samples (tissues, embedded paraffin blocks, and slides).

Preferred candidate profile MSc Microbiology with 1-5 years of experience in environmental monitoring in GMP regulated areas, with hands-on experience in operating microbiology instruments like water bath, weighing balance, pH meter, Hot air oven, Bio safety cabinets, HPHV Steam sterilizer, Dry block incubator. Role & responsibilities To perform Environmental Monitoring in required areas of GMP facility. To prepare Disinfectant solutions and Reagents. To handle the Microbiology instruments like water bath, weighing balance, pH meter, Hot air oven, Bio safety cabinets, HPHV Steam sterilizer, Dry block incubatorbut not limited to. To Receive, Storage and Handling of Microbiology consumables. To Perform fumigation/fogging in the clean rooms. To Sterilize the porous and non-porous goods loads. To Personnel gowning Qualifications for aseptic areas. To participate in media fill activities. To Prepare Environmental monitoring trends. Responsible for Stock verification and indents. To handle biological indicators and Bio balls and Endotoxin test kits. To perform NVPC monitoring in clean rooms. To perform sterilization and decontamination cycles on daily basis To Involve in regulatory audits and Customer audits.

Roles & Responsibilities Will be responsible for preparation and submission of dossiers for NCEs and NBEs and will present it to relevant internal and external stakeholders. will represent the company with Indian regulatory agencies, including CDSCO, RCGM, Central Bureau of Narcotics and Karnataka drugs control department. will be responsible for regulatory submission process, including CT-NOC, marketing authorization applications, NOC & test license. will follow up with regulatory agencies to obtain the approvals to support the regulatory timelines will identify and assess regulatory risks associated with product filing. will provide regulatory guidance to company personnel throughout the research and development process. Competencies: Understanding of various regulatory requirements for new drug development Presentation & Communication Skills Interpersonal Skills Proficiency in Kannada Desired Profile : M. Pharm/M.Sc. with 2+ yrs of experience in submission of dossiers to Indian Regulatory agencies Working experience of IND and NDA filing of NCE and NBE products

Preferred candidate profile M.Sc Organic Chemistry with 2-3 yrs. experience in Process /synthetic chemistry & 6-7 yrs. experience in API QA [ review of process development documents including KSM/KRM identification, specification proposal and stability reports. Role & responsibilities Prepare and Review Standard Operating Procedures and Guidelines for DQA. Review documents with respect to drug substance such as protocols, SOPs, test methods, data, BMR, BPR, ROAs, COAs and reports through collaboration with PRD, ARD and QC scientists, to achieve the highest quality from technical and compliance perspectives. Review process development documents including KSM/KRM identification, specification proposal, analytical method development/validation reports, stability protocols & reports, and safety studies. Responsible for investigations against laboratory Incidents, OOS, OOT encountered with aim of root cause identification and CAPA implementation. Responsible for assessing the impact, review and closure of Change control requests and Deviations. Responsible for CAPA implementations, verification of and effectiveness. Responsible for maintaining the Quality Metrics and preparation of Quality Metrics. Plan, execute internal audits, external audits and communicate audit schedules, outcomes to audit stakeholders ensuring CAPA appropriateness for closure, audit trending for continual quality improvement. Review and approval of Stability management activities of Drug substance and Drug products such as Stability Protocol, data and stability summary report. * Note : We are not looking for IPQA, CQA/Analytical QA personnel. Candidates with experience in review of process development documents including KM, KRM identification , specification proposals and API QA experience are required.

Role & responsibilities In the current role, the candidate will have to develop new cell therapy products and perform validations to take the product to the next stage. Extensive experience working with different types of immune cells and deep understanding of both innate and adaptive immune systems will be required. Previous experience in gene and/or cell therapy drug development teams will be preferred. Experience in design and delivery of genes using viral or non-viral transfer techniques. Design and construct of viral vectors using state-of-the-art molecular synthesis and cloning techniques. Experience in use of CRISPR/Cas9 or TALEN or other gene-editing tools Well-versed with different molecular biology techniques like cloning, sub-cloning, real-time and quantitative PCR, etc. Ability to multitask and contribute to multiple projects under demanding timelines while preserving integrity, accuracy, safety, and quality. The candidate should be proficient in verbal, written and presentation skills and previous experience in writing grants and research articles will be preferred. The candidate should have had experience in managing a team or working in a cross-functional group and interacting with clients/collaborators. The candidate needs to have leadership skills to gear a team towards excellence. Manage day to day activity of team members providing critical technical/scientific recommendations with effective trouble-shooting and innovative capabilities. The candidate should be able to effectively communicate and work closely in a highly matrixed team environment to advance companys cell therapy pipeline. The candidate will be expected to understand systems and processes pertaining to sterile practices, work ethics, safety, health, and environment. The candidate will have to be involved in preparation and participation during compliance monitoring inspections and regulatory agency interactions. The candidate must be involved in preparation and review of protocols, reports, regulatory documents, pertaining to program requirement. Competencies: Gene editing and molecular biology techniques Gene transfer Viral and non-viral methods for cell line generation Immunology/Immuno-oncology Genetics and Assays Preferred candidate profile Ph.D. (specialization in genetics and epigenetics related to Immunology/Immuno-oncology) with 1-2 years of experience in Gene Editing and Immuno-oncology and/or industry or M.Sc/M.Tech in Biotechnology with 8-9 years of experience in academia and/or industry

Job Summary: We are seeking a dynamic and driven Talent Acquisition professional to lead end-to-end recruitment and onboarding processes. This role is key to building a strong talent pipeline for niche and high-impact roles across the organization, ensuring our hiring strategies align with business growth and workforce planning needs. Key Responsibilities: Lead the entire recruitment lifecycle including manpower forecasting, budgeting, sourcing, interviewing, selection, onboarding, induction, and background verification. Develop and execute innovative hiring strategies to support rapid and sustainable business growth. Build strong talent pipelines for specialized and hard-to-fill roles by leveraging talent mapping, competitive intelligence, and market research. Partner with business leaders to understand workforce plans and translate them into effective sourcing strategies. Design and implement scalable recruiting programs that align with the organization's talent goals. Ensure full compliance with recruitment-related audits. Track and report key recruitment metrics such as lead time, selection ratios, budget adherence, and workforce demographics. Desired Profile: Proven experience in full-cycle recruitment across a variety of roles and levels. Strong business partnering skills with the ability to influence senior stakeholders. Demonstrated agility in working independently with minimal supervision, especially in fast-paced or evolving environments. Expertise in building hiring strategies and processes for niche technical functions. Excellent communication and interpersonal skills with a collaborative and proactive mindset. If you're passionate about hiring top talent and shaping recruitment strategies that fuel business success, would love to hear from you!

Job Description: Proffered Profile: Bachelors degree (BE/B tech) with 3-5 years of experience in IT QMS Compliance Specialist ensures alignment of all IT systems, processes, and documentation with internal Quality Management Systems (QMS) and applicable regulatory standards such as GxP, ISO 9001, 21 CFR Part 11, and EU Annex 11. This role plays a key part in audit preparedness, deviation management, and maintaining consistent quality across IT operations and projects. Key Responsibilities: Develop, implement, and maintain IT quality policies, SOPs, and work instructions in accordance with QMS. Ensure compliance of IT systems with relevant regulatory requirements (GxP, 21 CFR Part 11, GDPR, etc.). Collaborate with QA, Validation, and Business teams for development, qualification, and maintenance of IT systems as per CSV and QMS guidelines. Manage QMS elements such as deviations, CAPAs, change controls, audit trails, and periodic reviews. Participate in internal/external audits; coordinate documentation, evidence, and responses. Conduct IT quality risk assessments and support necessary remediation. Maintain accurate records of compliance activities, including SOP training and validation documentation. Deliver training programs to IT teams on QMS processes and compliance awareness. Support full lifecycle management of computerized systems (planning, validation, operation, retirement). Assist with vendor qualification and assessments for IT-related services. Required Skills and Qualifications: 3 - 5 years in IT compliance/QA/validation in a regulated industry Working knowledge of ISO 9001, GAMP 5, 21 CFR Part 11, EU Annex 11 Familiar with LIMS, ERP, MES, DMS systems Strong documentation and analytical skills Good understanding of ALCOA+ and data integrity Preferred Certifications: ISO Lead Auditor, Six Sigma, or other Quality Management certifications

Role & Responsibilities Will be responsible for managing Discovery projects end to end. Facilitate project team meetings and ensure accuracy and adequacy of documentation of project issues and action items. Handle minimum 3-4 (Early stage / Lead Optimization stage) internal or external programs and additional responsibilities (w.r.t processes / in-house applications). Co-ordinate project planning with respect to time and cost. ; co-ordinate with various functions of a project team for budget projections for approval and tracking of budgets/costs spent vs approved, assessing and reporting impact of variances. Lead and co-ordinate with respective functions for shipments, identifying reimbursable for monthly billing to clients (wherever applicable) and outsourcing studies (Non-GLP, GLP, GMP). Monitor resource allocation and utilization for assigned programs in consultation with function heads/Project team leads. Assess scope changes and risks to program delivery; flagging issues, making recommendations in consultation with team and executing agreed actions Provide timely communication of project/program status, issues and challenges to stakeholders and senior management Preferred candidate profile M.Sc. / M. Pharm / MTech & MBA with 4-6 years in project management with PMP certification, preferably from biotechnology/ Pharmaceutical sector Must have commercial /product launch experience Candidate with project management experience in Discovery Sciences would be preferred; should be adept at managing project milestones, budget and stakeholders. Should have excellent communication skills. ; Should have good negotiation skills & must have experience in MS project, MS Excel

M.Sc. (specialization in any Life sciences) with 4- 10 years relevant experience Experience in aseptic processing in GMP Classification and cell culture is (at least in mammalian cell culture) required; experience in the automated T-cell culturing process, washing, harvesting, and Cryopreservation is preferred. Hands-on experience or understanding in developing, manufacturing CAR-T cell therapy products is preferred. Experienced/Participated in aseptic process simulation, proficient in aseptic techniques, especially in aseptic filling of drug products, Biosafety cabinet operations, clean room behaviors, sterile welding, sealing, sterile transfer, etc. Good exposure or understanding of QMS aspects (Change control, Risk Assessment, Deviation, Preparation of Investigation report, and CAPA). In-depth understanding of Cell & Gene Therapy Manufacturing/development and associated regulatory guidelines. Roles & Responsibilities: Responsible for optimization of CAR cells manufacturing processes using normal human or patient-derived primary blood components, following ethical practices and QMS as per GMP guidelines Actively manufacture CAR-T cell therapy products by diligently prioritizing the lab functions to meet critical deadlines Establish and carefully execute transduction by viral vector and non-viral vector-based approaches, activation, and expansion of immune cells (T cells, NK cells, etc) isolated from clinical specimens without compromising sterility and quality parameters as per the guidelines and defined criteria by maintaining highest standards Able to communicate effectively in a highly matrixed team environment to advance the company's cell therapy pipeline Participate and assist in technical transfer and core R&D activities To review and prepare document SOPs, protocols, and reports pertaining to the program requirements Work closely with cross-functional teams to design and implement cell therapy processes and workflow for cell therapy platforms Provide critical technical/scientific recommendations for the manufacturing process improvements Work with vendors to evaluate raw materials and consumables for compatibility with the Manufacturing process Coordinate very closely with quality control, quality assurance, supply chain teams, etc, and strictly adhere to the project timelines by preserving integrity, accuracy, safety, and quality Prepare and participate in compliance monitoring inspections / regulatory agency interactions Able to troubleshoot experiments, record, analyze, interpret, and present the data in scientific meetings Understanding of systems and processes regarding sterile practices, work ethics, safety, health, and environment Ability to work off-shift and irregular hours as required Competencies: CAR-T manufacture under GMP settings Proficient in Aseptic Operations Culture of T cells/NK cells and handling of viral vectors Statistical analysis, Presentation & Communication Skills Documentation and Report Writing Interpersonal Skills Team Player / Team Management

Role & Responsibilities Will be responsible for managing Discovery projects end to end. Facilitate project team meetings and ensure accuracy and adequacy of documentation of project issues and action items. Handle minimum 3-4 (Early stage / Lead Optimization stage) internal or external programs and additional responsibilities (w.r.t processes / in-house applications). Co-ordinate project planning with respect to time and cost. ; co-ordinate with various functions of a project team for budget projections for approval and tracking of budgets/costs spent vs approved, assessing and reporting impact of variances. Lead and co-ordinate with respective functions for shipments, identifying reimbursable for monthly billing to clients (wherever applicable) and outsourcing studies (Non-GLP, GLP, GMP). Monitor resource allocation and utilization for assigned programs in consultation with function heads/Project team leads. Assess scope changes and risks to program delivery; flagging issues, making recommendations in consultation with team and executing agreed actions Provide timely communication of project/program status, issues and challenges to stakeholders and senior management Preferred candidate profile M.Sc. / M. Pharm / MTech & MBA with 4-6 years in project management with PMP certification, preferably from biotechnology/ Pharmaceutical sector Candidate with project management experience in Discovery Sciences would be preferred; should be adept at managing project milestones, budget and stakeholders. Should have excellent communication skills. ; Should have good negotiation skills & must have experience in MS project, MS Excel

Preferred candidate profile: PhD (Organic chemistry / Medicinal chemistry) with 5 -6 years of experience in antibody drug conjugates (ADC) development Roles & Responsibilities: Must have hands on experience in linker- payload synthesis and overall understanding of ADC. Should be able to design and execute synthesis of complex drug linkers and ADC payloads. Should have proficiency in characterization and analysis of synthesized molecules using analytical techniques such as HPLC, LC-MS and NMR. Thorough understanding of linker chemistry and latest development in the space. Efficient employment of structure-based drug design principles and integrate with other experimental data collected in the design of new linkers. Mentor and manage team members for high performance and scientific growth. Collaborate with project team members and communicate progress against goals in a multidisciplinary setting: chemistry, antibody engineering, biology, pharmacology, DMPK, and external collaborators. Accurate documentation of experiment and maintaining a well-organized laboratory notebook (LNB). Understanding of systems and process related to safety, health, and environment (SHE).

Preferred candidate profile Chartered Accountant with 3-5 years of relevant experience in Taxation, GST, Analytics, Budgeting from any industry Role & responsibilities Preparation of annual budgets for key business functions. Analysis of expenses and providing reasons for variance when compared with budget. Income tax computations and payment of advance tax, self- assessment tax. Prepare income tax submission documents for income tax assessment and maintain proper documentation as per requirements of income tax act. Structure transactions as per GST in a manner beneficial to the company. Maintain books and documents as per the requirements of GST. File of various forms e.g. input credit, output etc under GST and monthly reconciliation of credits. Attend assessment notice from departments and preparation of submission documents. Timely payment of GST under normal provisions of the Act and under reverse charge mechanism. Compliance with Various statutory norms and filling of related forms. Evaluate of transactions for applicability of GST and optimisation. Participate in monthly books closure activities including preparation of provision for key business functions. Prepare relevant MIS for the department on project budgets, actuals, etc. Support review and processing of vendor invoices for key business functions. Must have good working knowledge of MS Excel, MS PowerPoint and MS Word. Experience of working with SAP ERP would be preferred. Extensively collaborate within Clinical department, SCM, Legal and other stakeholders. Good analytical skills to diligently prepare the deliverables within the given timelines. Good communication and presentation skills to effectively interact with various stakeholders

Preferred Candidate Profile: M. Pharm (Pharmacology / Pharmaceutical Analysis) / M.Sc. (Biochemistry / Pharmaceutical Chemistry / Analytical Chemistry) with 5-8 years or Ph.D. with 2-5 years experience. Role & responsibilities Experience in designing, performing, and interpreting metabolite identification studies- Invitro and Invivo. Proficient in using LC-MS/MS, HRMS, and other analytical techniques for identification of metabolites and its soft spots. Ability to analyze complex data sets and structural interpretation for Phase-1, 2, and 3 metabolites. Strong understanding of drug metabolism principles and pathway. Experience with regulatory documentation and submissions Experience in DMPK concepts and provide insights to project teams. Represent the group in internal and external meeting. Ability to work effectively in a team environment. Strong understanding of various concepts of DMPK in large molecule/ADC with excellent communication skills, driving innovation, managing teams is added advantage Responsible for preparation of relevant SOP, protocols, reports, etc. to support various regulatory and non-regulatory submission.

Preferred candidate profile Chartered Accountant with 0-2 years (OR) B.Com & MBA Finance with 5-7 yrs. of relevant experience in Budgeting & Planning, Fixed asset management & SAP ERP from any industry Role & responsibilities Preparation of annual budgets for key business functions. Analysis of expenses and providing reasons for variance when compared with budget. Participate in monthly books closure activities including preparation of provision for key business functions. Preparation of latest estimates by collating the information from various vendors, business & cross functional teams. Review of agreements and understand the business extensively. GST Input tax credit reconciliations and communicating with vendor for resolving the variances and support in various audits. Prepare relevant MIS for the department on project budgets, actuals, etc. Follow up with external stakeholders (sites, vendors, collaborators) to understand work done so far, expected date of invoices, and estimated future expenses over the current Financial Year. Support review and processing of vendor invoices for key business functions. Must have good working knowledge of MS Excel, MS PowerPoint and MS Word. Experience of working with SAP ERP would be preferred. Good analytical skills to diligently prepare the deliverables within the given timelines. Good communication and presentation skills to effectively interact with various stakeholders. Working model: Work from Office (all 5 days) Work Timing: 9 to 6 p.m.

Preferred candidate profile M. Pharm (Pharmacology) / M.Sc. (Biochemistry / Pharmaceutical Chemistry) with 6-9 years or Ph.D. with 2-5 years' experience in PBPK & PK/PD modelling & Gastro plus; Simcyp software Role & responsibilities Experience in the development and application of pharmacometric models to support drug development and regulatory submissions Extensive experience with non-linear mixed effects modelling Proficient with software tools like PBPK models, Phoenix, R, PoPK, QSP modelling or similar platforms Strong background in pharmacokinetics/pharmacodynamics (PK/PD) modelling, First-in-human dose predictions. Collaborate with clinical pharmacology, biostatistics, and other interdisciplinary teams to inform clinical trial designs and data analysis Develop and implement model-based strategies to optimize dosing regimens and therapeutic outcomes Ensure the accuracy and quality of pharmacometric analyses and reports Engage with regulatory agencies and prepare regulatory submission documents related to pharmacometric analyses Stay abreast of the latest developments in pharmacometrics and incorporate new methodologies and technologies as appropriate Present findings and strategies to the project team meeting and cross-functional teams. Ability to work effectively in a team environment.

Preferred candidate profile M. Pharm (Pharmacology / Pharmaceutical Analysis) / M.Sc. (Biochemistry / Pharmaceutical Chemistry / Analytical Chemistry) with 3 - 6 years experience in Bioanalytical DMPK & Invivo PK. Role & responsibilities Planning and execution of invivo preclinical pharmacokinetic studies, invivo tissue distribution & mass balance studies in rodents. Expert in method development of NCEs using LC-MS/MS system Well verse with extraction techniques of molecules from various matrices like plasma/urine/tissues Experienced in surgical skills for rodents PK, excretion studies Conduct Bioanalysis of samples from in-vivo pharmacokinetic, tissue distribution studies, PK-PD & TK studies through LCMS/MS Prepare protocols and SOPs in line with industrys best practices Very strong in basics of all instruments, principles of chromatography, sample processing Knowledge of Phoenix WinNolin software will be added advantage