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

ResponsibilitiesDevelop and implement educational programs and strategies to maintain high standards of teaching and learning. Oversee the recruitment, training, and evaluation of staff to ensure a qualified team. Establish a safe and inclusive learning environment for all students and faculty members. Build and maintain relationships with students, parents, and the wider community. Manage the budget and resources effectively to support the academic goals of the institution. Qualification & ExperiencePh.D. in Allied Health Sciences / Healthcare / Life Sciences (preferred) Master’s degree in relevant discipline (mandatory) Minimum 10–15 years of teaching experience, including 5+ years in a leadership role Strong knowledge of healthcare education regulations in Ind Strong leadership and communication skills. In-depth knowledge of educational policies, curriculum development, and academic standards. Ability to make strategic decisions and solve problems effectively.

ResponsibilitiesConduct thorough nursing assessments, considering clinical condition, pain, hygiene, allergies, safety, and overall patient status. Develop nursing care plans each shift based on patient needs, safety, diet, and assessment findings. Establish priorities for nursing needs based on assessment, identified problems, and estimated length of stay. Implement admission protocols, maintain accurate records, and update patients and families. Demonstrate knowledge of AIDET (Acknowledge, Introduce, Duration, Explanation, Thank) and GST (Greet, Smile, Thank). Utilize effective communication skills in reporting pertinent information on time. Deliver comprehensive nursing care to critically ill patients including assessment, medication administration, monitoring, and documentation. Collaborate with physicians and multidisciplinary teams to implement individualized care plans. Perform advanced clinical procedures such as ventilator management, hemodynamic monitoring, and CRRT. Respond promptly to changes in patient condition with timely communication and intervention. Educate patients and families regarding treatment plans, disease management, and medication adherence. Comply with hospital policies, infection control protocols, patient safety standards, and confidentiality regulations. Engage in continuous professional development and training. Maintain valid nursing registration and medication administration records. Adhere to all safety policies and uphold Max Healthcare values and grooming standards.

ResponsibilitiesConduct thorough nursing assessments, considering clinical condition, pain, hygiene, allergies, safety, and overall patient status. Develop nursing care plans each shift based on patient needs, safety, diet, and assessment findings. Establish priorities for nursing needs based on assessment, identified problems, and estimated length of stay. Implement admission protocols, maintain accurate records, and update patients and families. Demonstrate knowledge of AIDET (Acknowledge, Introduce, Duration, Explanation, Thank) and GST (Greet, Smile, Thank). Utilize effective communication skills in reporting pertinent information on time. Deliver comprehensive nursing care to critically ill patients including assessment, medication administration, monitoring, and documentation. Collaborate with physicians and multidisciplinary teams to implement individualized care plans. Perform advanced clinical procedures such as ventilator management, hemodynamic monitoring, and CRRT. Respond promptly to changes in patient condition with timely communication and intervention. Educate patients and families regarding treatment plans, disease management, and medication adherence. Comply with hospital policies, infection control protocols, patient safety standards, and confidentiality regulations. Engage in continuous professional development and training. Maintain valid nursing registration and medication administration records. Adhere to all safety policies and uphold Max Healthcare values and grooming standards.

ResponsibilitiesReleasing or rejecting all APIs including intermediates Ensuring the compliance of all the systems as per GMP requirement Approving all specifications and master production instructions Investigation and closure of all deviations & OOS Approving all procedures affecting quality of RM/IM/API Conducting self-inspections and internal audit Conduction vendor evaluation Review of changes that potentially impact intermediates or API Quality Reviewing of validation protocols and reports Investigation of quality related customer complaints and returned goods Review of preventive maintenance and calibration of equipment's To execute Risk Assessment Activity Review of stability data Performing product quality review Facing customer and regulatory audits Ensuring proper responses to the customer and regulatory queries Checking of QA procedure In absence of Head-QA, will be responsible for QA related activities

ResponsibilitiesIndependently lead end-to-end formulation development and process design for personal care products across formats (creams, lotions, gels, deodorants, body oils, cleansing) Drive fast-track NPD ensuring OTIF timelines and First-Time-Right (FTR) commercialization Translate marketing concepts and consumer insights into technically feasible, cost-effective, and scalable formulations Manage multiple projects simultaneously, ensuring timely delivery and stakeholder alignment Perform technical scoping including literature review, benchmarking, ingredient selection, and formulation strategy Apply DoE and scientific approaches to optimize formulations for performance, stability, manufacturability, and cost efficiency Conduct trend mapping and competitive intelligence to drive innovation and differentiation Identify opportunities and drive innovation, cost optimization, and sustainability initiatives Execute formulation trials, stability studies, and product evaluations considering performance, cost, packaging, regulatory, and safety requirements Lead pilot batches, scale-up, and technology transfer in collaboration with manufacturing and supply chain teams Collaborate with cross-functional teams (Marketing, QA, Analytical, Regulatory, Procurement, Supply Chain) and manage external stakeholders (vendors, third-party manufacturers, labs) Ensure compliance with GLP, GDP, regulatory, and internal quality standards, maintaining audit-ready documentation Create product demos and technical tools to support business and product understanding 

ResponsibilitiesStreamlining time & absence process for PAN India PPS Sites Preparing process notes for all the processes managed by GEEC; Periodically evaluate the current practices, suggest areas of improvement, and update standard operating procedures Responsible for end-to-end HR Operations deliverables Provide consistent Employee Experience Implementation/ support of HRIS Projects HRIS Management of Employee Records (Oracle Fusion) End-to-End Data Management of Employees Support Internal, External Audits and Risk related processes Query Management

ResponsibilitiesPrepare, compile & review product quality (CMC) & other regulatory documents to support product development or submissions to various countries across the world for product registrations or post approval life cycle maintenance. Create and/or revise raw material and packaging specifications, and other associated documents. Coordinate and interact with cross functional teams/departments for evaluation/impact assessment of change control, review implementation strategy and required documentation governing the change and manage OOS, OOT or other product related changes. Support Financial Data Management, Business Plan file creation and maintenance, Supplier data management and PO creation as required. Support for creation and update of global labeling documents, QC and other associated activities for the labeling projects Support stability data evaluation & report preparation, dissolution profile evaluation etc. Perform literature survey and preparing of various regulatory documents in support of excipients, APIs and/or drug products. Coordinate with stakeholders to understand and support import license requirements, investigation report drafting, record management and document coordination with internal and external department. Responsible for specifications setting/justification, ensuring the Quality level for Laboratory support, perform Computerized System Validation (CSV) and upgradation of existing systems/software. Seek guidance from other team members and manager as needed, and keep up to date knowledge of various regulatory guidelines required for pharmaceutical product registration and product life cycle maintenance. Implement use of consistent, efficient, and quality processes to meet timelines and deliverables according to regulatory requirements standard operating procedures and maintain a culture of high customer services. Japanese language expert (minimum JLPT N3 certified professional) with experience in Japanese business email and client communication. Support Japanese regulatory and supplier correspondence, translations (Japanese ? English), and coordination with RA teams.

ResponsibilitiesLead the overall product life cycle from conception to launch, aligning product vision with customer needs and business goals, for multiple products. Conduct market research and analysis to identify trends, opportunities, and competitive threats in the life sciences sector. Conduct market research to identify vendors available in this space and analytically decide between build vs. buy. Define (hands-on) and prioritize product requirements, features, and functionalities in collaboration with data management operations teams, engineering, data and other teams. Develop and maintain product roadmaps, ensuring clear communication and alignment across all stakeholders. Monitor and evaluate product performance metrics, adjusting strategies as necessary to achieve success.Qualification & ExperienceBachelor’s degree in engineering, Life Sciences, Health Care, or a related field. Extensive experience working on standard EDC products like Medidata, Veeva, CTMS and other similar systems Knowledge of CDISC, ICH frameworks and keeps track of recent changes and advancements Experience of understanding data concepts for data management systems and Business Intelligence products

ResponsibilitiesEnsures that all allocated projects are carried out in strict accordance with the relevant protocols, global harmonized SOPs, and the specified standards of GCPs. Demonstrates capability to read and follow study timelines for on-time deliverables. Potential to assist with inputs on study design or capable to make suggestions to study timelines when warranted. Assist with review of clinical trial data in accordance with Data Management Plans and/or Data Review Guidelines and raise queries to resolve erroneous, missing, incomplete data. Run and execute additional programs (special listings, reconciliation discrepancy listings, etc.) used to support the review of clinical trial data. Generate, resolve and track queries to address problematic data identified during aggregate data review activities. Interacts with other project team members to support the set-up, maintenance, and closure of the Data Management aspects of the project and attend meetings as required. Generate and QCs data listings for internal data review. May assist or create dummy data to test edit checks and to test database screen design and functionality. Assist or create dummy data to test SAS reports and data listing. Demonstrates the ability to review Edit Check Specifications and Database specifications. Post Data Management documentation and data management related administrative tasks as requested, including maintenance of eTMF as required. Runs study status reports in preparation for Sponsor meetings and to deliver on specific Sponsor request. Assist with the completion of Database Lock and Unlock activities. Supports the training of new staff on project specific Data Management processes. Performs any other duties as assigned.Qualification & ExpeirenceUniversity / college degree (life sciences, health sciences, information technology or related subjects) or a certification in allied health professions from an appropriate accredited institution. Fluent in English, both written and verbal. Experience (Minimum Required): 3 to 5 years of relevant work experience with increasing responsibility in data management with knowledge of one (1) or more therapeutic areas. Demonstrated time management skill and ability to adhere to project productivity metrics and timelines. Knowledge of medical terminology is preferred. Knowledge of effective clinical data management practices.