ResponsibilitiesResponsible for managing QA documentation, ensuring GMP compliance, and supporting quality systems through effective handling of SOPs, BMR/BECR review, validation and qualification activities. Oversees document control, vendor qualification, calibration and maintenance coordination, and ensures timely closure of deviations, change controls, and CAPAs while maintaining data integrity and audit readiness across all QA operations. Issuance, archival and retrieval of documents. Issuance of Control coples to respective dept. Destruction of the GMP documents once the retention term has passed and controlled coples of the obsolete GMP documents. Tracking of all QA documents. 5. Maintaining backup of QA softcoples. Maintaining SOP/s with proper indexing. Preparation and review of SOPs Management of QA Stationary (Controlled Coples and logbooks) Dispatch and line clearance activity.

Responsibilities Prevent incidences across Unit to ensure employees and stakeholder¢â?¢s safety  Assess and Improve emergency preparedness across Unit to reduce impact of Incidences to human and property Execution of the planned Activity, promotional Activity and improvement and Statutory complianceQualification & ExperienceScience graduate in chemistry/ Diploma or Degree with Diploma in Advance industrial safety Relevant Work Experience 2 years of safety experience in Pharma or chemical industries

ResponsibilitiesResponsible for Quality metric data review along with critical & repeated quality issues, and status of quality initiatives/programs to be presented to senior management as part of Governance Meetings. Coordinate and follow-up with site representatives for updates to actions points and QMS data. Plan & track regular interactions with sites on overall inspection readiness plans as per compliance requirements. Tracking of the 30, 60, 90 day improvement action plans with sites including the CAPA generated as part of Internal Audits & Governance Meetings. Providing inputs on Corporate Quality SOPs/Guidelines to comply with current regulatory guidance and requirements. Support for any organizational corporate initiative assigned. Qualification & Expeirnece10-15 years in QA, Compliance, GMP, Auditing, KPI management. Education Graduation in Pharmacy or Science Post Graduation in Pharmacy or Science

ResponsibilitiesComply with all cGMP, GxP or any other regulatory requirements, including EH&S requirements. Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task. Conduct all tasks/ activities as per the applicable SOPs. Report any difficulty or deviation in following the procedures/instructions to immediate Supervisor/Managers. Report any quality concerns or suggestions for improvements to Supervisors/ Managers. Responsible to complete the assigned trainings applicable for workgroup “Warehouse-Raw And Packing Materials-GOA” in the L2LMS (SABA). Responsible for review and updation of online documentation in Warehouse as per SOP.Qualification & Expeirnece2 to 4 years Education Graduation in Chemistry or Analytical Chemistry

ResponsibilitiesMethod development and qualification, characterisation of Lupin’s products and reference medicinal products Documentation related: Preparation and review of documents, data review Compliance related activities: CSV coordinator Instrument related: Equipment qualification, weighing balance performance coordination Maintenance: Maintenance of GLP, GDP and support, supervision and management Instrument maintenance: CD, SPR, Octet, FTIR, BLI, refrigerator and miscellaneous, equipment ID generation. Technolgy Transfer , Complaince with EHS and safety Qualification & Expeirnece5-6 years of experience in protein structure biology Education Masters in Biology or Biology Post Graduation in Biology or Biology

ResponsibilitiesAssist senior staff with daily tasks and projects, adhering to company policies and safety regulations. Learn and apply standard operating procedures (SOPs) in relevant departments such as manufacturing, quality control, research and development, or supply chain. Participate in training sessions and workshops to enhance knowledge and skills in pharmaceutical processes and technologies. Maintain accurate records and documentation as required for assigned tasks. Communicate effectively with team members and supervisors, reporting progress and any issues encountered. Demonstrate a strong commitment to learning and professional development. Contribute to a safe and productive work environment.

ResponsibilitiesDevelop, maintain, and update HR MIS reports and dashboards. Ensure accuracy and timeliness of data inputs across HR systems. Support automation initiatives to reduce manual reporting and improve visualization. Provide data extracts and analysis for audits, compliance reviews, and leadership reporting.Qualification & ExpeirenceBachelor’s degree in engineering, HR Technology, Data Analytics, or related field Experience 3–5 years of experience in HR MIS, reporting, audits, or quality management Hands-on exposure to HR systems (SAP SuccessFactors, Workday, Oracle HCM) Strong proficiency in MS Excel, PowerPoint, PowerBI Knowledge of compliance frameworks and audit processes preferred Experience in financial reporting, cost tracking, and budget compliance Implementing and managing HR technology solutions like chatbots, portals, or MIS tools

ResponsibilitiesResponsible for managing QA documentation, ensuring GMP compliance, and supporting quality systems through effective handling of SOPs, BMR/BECR review, validation and qualification activities. Oversees document control, vendor qualification, calibration and maintenance coordination, and ensures timely closure of deviations, change controls, and CAPAs while maintaining data integrity and audit readiness across all QA operations. Issuance, archival and retrieval of documents. Issuance of Control coples to respective dept. Destruction of the GMP documents once the retention term has passed and controlled coples of the obsolete GMP documents. Tracking of all QA documents. 5. Maintaining backup of QA softcoples. Maintaining SOP/s with proper indexing. Preparation and review of SOPs Management of QA Stationary (Controlled Coples and logbooks) Dispatch and line clearance activity. Review of BMR/BECRPerform Qualification for new Equipments/Existing Equipments Ensure & Co-ordination of area validations. Reviewing of calibration /PM Schedules. Preparation of VMP &validation Documents Handling of Vendor Qualification Activities. Any other work assigned by HOD/Second line. Involving in handling Deviations, Change Control and related CAPAS. To ensure data integrity compliances while performing activities

Responsibilities• Assist in establishing and implementing goals, objectives, policies, procedures and systems.• Gather and report fiscal, statistical and analytical data including audit compliance.• Assist in developing cost-effective administrative and operational policies.• Plan and coordinate daily work assignments and operations.• Resolve administrative and operational issues and escalate appropriately.• Ensure compliance with regulations and standards.• Work with medical staff to ensure quality patient care and confidentiality.• Prepare duty rosters for staff.• Participate in quality improvement initiatives and protocols.• Ensure operational quality and patient safety.• Support smooth functioning and overall performance of the hospital.Qualification & Experience•  Work Experience 10+ years• Qualification BHMS/BAMS/MBBS/MBA/ MHA

ResponsibilitiesManaging complete Radiation Safety Officer (RSO) duties, including operation and compliance of eLORA system and regulatory documentation Implementing radiation safety guidelines, institutional radiation protection program, and ensuring compliance with AERB and international standards Ensuring adherence to ALARA principles and maintaining radiation safety culture in the department Performing routine QA & QC of radiotherapy and imaging equipment including linear accelerators, CT simulators, and brachytherapy systems Handling external beam radiotherapy systems such as Elekta Infinity Linear Accelerator, Varian TrueBeam Linear Accelerator, Accuray TomoTherapy Hi-Art System, Accuray Radixact System, and Siemens Bhabhatron-II Supporting advanced radiotherapy techniques including 2D, 3DCRT, IMRT, IGRT, SRS, SBRT, TBI, HBI, and TSET Working on treatment planning systems such as Eclipse Treatment Planning System, Monaco Treatment Planning System, Tomotherapy Hi-Art Planning System, Precision Treatment Planning System, and Prowess Panther Treatment Planning System Performing brachytherapy procedures using MicroSelectron HDR Brachytherapy System with planning in Oncentra Brachy Treatment Planning System including intracavitary applications, MUPIT, APBI, and dosimetry Managing CT simulation and imaging systems including GE Healthcare 4D CT Simulator and Philips Big Bore 4D CT Scanner Conducting radiation safety training, audits, incident management, and ensuring compliance with regulatory and clinical safety standards