ResponsibilitiesTo Provide Quality clinical Care to PatientsTo practice evidence based medicine awareness regarding patient {Investigation- (profile/reports/plan) {Treatment- (details/drug procurement)} {Drug Allergies/ patient history}To ensure Emergency Preparedness & Response Treatment/ Procedure/ Investigations)To ensure timely attention and intervention for any query or requirement from the IP patient. To ensure that the IP rounds are duly done and the patients are attended to empathetically.To comply with patient protocols (OP-IP/OT/ Diagnostics/ ICU/ Triage) & document patient File/ Prescriptions/requisitions (legible/ complete)To ensure MLC notification / documentation and statutory compliance.To ensure Documentation at the time of DischargeTo complete all OP & IP records on time with accuracy. To ensure availability/ good-working condition of the Life saving Drugs and Equipment (In conjunction with BME and report delayed response). To ensure proper Bio Medical Waste Management & follow Infection Control protocolsTo follow ethical Medical practice and to ensure clear and prompt communication with the Admitting as well as Referral Consultants.To be well groomed, punctual & adhere to company policies and practices.To have complete orientation of IMS and NABH system. To have complete Awareness about Disaster Management Programme (DMP) of the hospital.To Comply with patient safety policyThe role required to do shift duties including night shifts and emergency duties on call as per monthly planned roaster Qualification & Experience MBBS

Qualification & ExperienceQualification: MBBS Post PG: DM (Medical Oncology) Experience: 2 to 5 yrs 

ResponsibilitiesResponsible for preparation & review of the master documents of sterile manufacturing for parenteral facility. Responsible for preparation and review of protocols and reports based on the requirements. Responsible for document management and preparation like BMR’s, BPR’s, master SOP’s etc. Responsible for the handling of change control, deviations, CAPA, investigation etc. Responsible to give training to all the subordinates, technicians and operators of the department. Responsible for Audit and compliance on manufacturing shopfloor. Knowledge of kaizen and continuous improvements.Qualification & ExperienceQualification: B.Pharm/M.Pharm candidate with minimum 3-5 years experience in manufacturing QMS/Process review/Compliance.

Responsibilities• You will be responsible for conducting an in-depth evaluation of the competitive landscape and identifying source of growth for assigned brands. This involves defining key success factors and requirements necessary for a successful perception building for brands handled in covered therapy areas.• You will define the commercial strategy for the product early on, including market access strategy and plan, and creating marketing materials.• Your role includes supporting countries in generating local market access, if required, and executing market research activities to evaluate market potential and strategies.• You will also identify and mitigate potential hurdles, threats, and risks, both at the front end and back end.• You will ensure cross-functional alignment on forecasts, product volume capacity requirements, and launch preparation, including recommendations for long-term product-specific capacity investments.• You will be accountable for the product's profit and loss (P&L), including profitability calculation reflecting product-specific sales and marketing costs and other investments before and after handing over to markets.• Your role includes defining and monitoring the life cycle management strategy with development teams and optimizing product allocation for products under supply constraints.• Your responsibilities extend to portfolio optimization and rationalization, involving commercial growth strategies, portfolio rationalization, and conducting in-depth costing analysis and improvement strategies to enhance overall performance.Qualification & Experience      • Educational qualification: B.Pharm./M.Pharm. and MBA• Minimum work experience: 2-4 years of experience in Brand Management• Proficiency in managing and coordinating development projects from initiation to completion, including setting project goals, timelines, resource allocation, and risk management.• Experience in preparing for new product launches, including market analysis, competitor research, launch strategy development, and coordination with various departments to ensure successful market entry.• Expertise in overseeing the entire lifecycle of commercial products, including product planning, pricing, positioning, and promotion to maximize profitability and market share.• Experience in understanding market research, including market trends, customer preferences, and competitor activities for strategic decision-making.• Knowledge of market access strategies and marketing tactics to ensure products are accessible to target markets and effectively promoted to healthcare providers, payers, and patients.• Proficiency in sales and marketing strategies, including customer relationship management, lead generation, sales forecasting, promotional campaigns, and sales performance analysis.• Ability to collaborate effectively with cross-functional teams, including R&D, marketing, sales, finance, and regulatory affairs, to achieve project objectives and deliver end to end results.• Strong leadership and communication skills, with the ability to influence stakeholders at all levels.• Critical thinking and problem-solving skills for investigations and process optimization.• Strong strategic thinking and decision-making skills.• Attention to detail and ability to multitask in a fast-paced environment.

Responsibilities•Ensure optimum functional performance, calibration, quality assurance and maintenance of RT equipments•To plan new installation and modify existing ones (where necessary from regulatory points of view). •To prepare Technical Specification for purchase of new RT equipments, their Acceptance and Commissioning.•To coordinate with consultants, equipments suppliers, their engineers, hospital Bio-Medical &maintenance departments and regulatory authorities.•To supervise source transfer operations of Brachy therapy unit and its Calibration.•Supervise & Coordinate with all concerned for simulation, planning and execution of planned treatment for external beam radiotherapy and Brachytherapy. •To establish and operate, approved quality assurance program for all equipments and procedures, daily, weekly, monthly, biannually as required •Obtain regulatory permission for operation of RT equipments from Competent Authority (AERB).•To establish and operate, quality assurance program for all RT equipments and procedures- daily, weekly, monthly, biannually as required.•Patient specific dosimetry & QA and maintain their records•Inventory & Disposal of Brachytherapy Sources•To maintain Equipment log books•CT, MRI & PET Image data processing for RT planning•Radiation monitoring of RT , X-ray & CT Installations•Personnel monitoring of Radiation workers & maintain Dose Record •To calibrate all radioactivity and dose measuring instruments and dosimeters and ensure their traceability to national standards.•Coordinate Radiation Safety committee meetings as Member Secretary and send reports to AERB.•Maintain health records of all radiation workers•Prepare Annual Status Reports of Radiation Safety in RT dept .according to AERB / BARC regulation.•Monitoring High Dose I-131 therapy patients in NM dept..•To ensure Display of Radiation Symbols at Radiological installations.•To keep of survey records including layout drawings, records of over exposures occurred if any and the action taken for remedy, records of radiation emergencies occurred if any and steps taken etc.General AdminstationQualification & Experience•Required Qualification M.SC

Qualification & Experience  Department : Oncopathology Qualification DM/PDCC in Oncopathology    Experience  0-3 Years   

Responsibilities• Implementation of hospital's /medical services vision & philosophy.• Infection control, Health care waste management, awareness of patients rights & safety issues, relationship building.• Supplement/take charge in case the vertical is on leave/absent etc.• Strategic inputs in her/his vertical & should forward recommendation for continuous improvement in the vertical.• To prepare Discharge summaries for all assigned patients. Discharge summary shall be prepared and updated atleast a day prior to expected discharge date. Discharge Summary must be complete in all aspects with accurate diagnosis details, hospital course, procedures carried out, significant tests, medications prescribed and follow up appointments. Once the discharge is confirmed by consultant, ensure that the updated discharge summary is approved and signed by the consultant in eHIS.• To provide the best possible prompt medical care to all patients in the specialty.• To work out all admitted patients in Day care & Ward, to take detailed history.• Check Chemotherapy prescription orders, verify and also check actual drug dosages & method by which it is given.• Supervise chemotherapy administration.• Networking with other Deptt. for any procedures, surgery, cross consultations.• To prepare Discharge summaries.• Discussion with patients regarding chemotherapy related issues.• To assist / perform Bone marrow procedure, lumber puncture.• To enter Patient related details in HIS like day to day notes, patient history, discharge notification etc.• To fill proformas, estimates for TPA’s etc, to keep a second copy of all the forms sent for such purpose in the Patient record file.• To ensure no drug wastage esp. during Chemotherapy.• To ensure waste management of all cytotoxic & biomedical waste as per state pollution control board.• To write progress notes of the patients in the records at least twice in one shift. The notes should be relevant to the patient current health status & treatment should reflect the future plan in compliance with the admitting consultant.• To liaise with the admitting consultants & to start the follow up treatments.• To coordinate all the references with other specialists if desired.• To ensure all the investigations are sent & the reports are interpreted & inform the concerned consultants. To ensure all related follow up including any change in the line of treatment on the basis of the reports of the investigations.• To give bedside over to the reliever while going off duty.• To ensure the diets of the patients are ordered as per the recommendations.• To ensure that the medicines to the patients are delivered as per the prescriptions.• To counsel all the discharged patients for further follow ups & to handover the discharge summary. The second copy of the same should be countersigned by the patient or the attendants & to be kept in the patient record file.• To take round with all the Consultants, Classified Specialists, Gr. Specialists in the specialty & to document the instructions & to ensure their compliance.• Collective rounds with the verticals, subordinates & to ensure all preventive & corrective measures to maintain the highest standards of patient care & service delivery.• Should facilitate all audits in the concerned areas & answer all their queries.• Inventory management, In addition to that to ensure systems to avoid wastages/pilferages/thefts etc.• To ensure SOP’s of the Medical Services be implemented.Qualification & Experience  • Education A recognized degree from Medical Council of India. Must be registered with State/Medical Council of India.• Experience 0- 1 year of relevant experience in the concerned specialty in a Super/Multi Specialty hospital is preferable.

ResponsibilitiesPerform radiation treatment planning, dose calculations, and plan verification.Conduct patient-specific QA and treatment delivery verification.Perform routine QA, calibration, and commissioning of radiotherapy equipment.Ensure compliance with radiation safety regulations and licensin requirements.Conduct radiation surveys, area monitoring, and shielding evaluations.Monitor occupational radiation exposure and maintain dose records.Maintain QA, dosimetry, and radiation safety documentation.Manage radiation protection programs for patients, staff, and the public.Coordinate regulatory inspections, audits, and compliance activities.Investigate radiation safety incidents and implement corrective actions.Qualification & ExperienceM.Sc. Medical Physics / Radiological Physics or equivalent qualification recognized by AERBValid RSO Certification as per AERB requirementsExperience in Radiation Oncology and Radiotherapy Physics preferredKnowledge of LINAC, Treatment Planning Systems, Dosimetry, QA, and Radiation Safety regulationsStrong documentation, compliance, and regulatory coordination skills

ResponsibilitiesDevelopment of marketing and promotional plans for products to support the end consumer’s need Monitor business performance and support the portfolio with the help of regular tracking Market intelligence through primary research and customer connect Writing and executing strategic business and marketing plans in collaboration with important prescribers, opinion leaders, round tables, and other advisory groups Joint financial responsibility for budgets (advertising and promotion, conferences and symposia, sales brochures and other product documentation, website content, literature), as well as analysis of budget income and costs; initiating and coordinating marketing activities and projects Presentation to staff and training field staff for the same Visiting national and international congresses, hospitals, and key opinion leaders (KOLs); Translating the corporate brand strategy in close collaboration with headquarters, together with logos and visuals, working with corporate product budgets (approval for expenditure on projects, local communication strategies), and providing input into corporate product strategy; Discussion partner for first, second, and third-line professionals such as medical specialists, pharmacists, and other medical professionals, and for other DMU members (decision-making units) such as local and national formulary committees and insurance companies; Organizing advisory councils, acting as a discussion leader or chairman, or giving product presentations. Collaboration with internal & external media to ensure the proper execution of strategiesQualification & ExperienceB. Pharm / M. Pharm & MBA Experience 7 to 12 years previous work experience.

Responsibilities• Knowledge of 3D CRT, IMRT, IGRT, Stereotactic Radio Surgery, Stereotactic Radiotherapy and TBI planning.• Ability to perform IMRT and IGRT plans within stipulated timelines.• Ability to create treatment plans on alternate machines to prevent treatment interruptions.• Ability to work in assigned shifts based on departmental workload. Plan radiation treatments for cancer patients and perform dose calculations.• Ensure accurate measurement of radiation output from sources used in cancer therapy and perform patient dosimetry.• Investigate equipment performance and organize quality control practices.• Design radiation installations and implement controls for radiation hazards.• Ensure radiation safety and design shielding for treatment rooms.• Ensure teletherapy machines, scanners and computers operate safely.• Perform machine acceptance testing.• Consult with senior physicists, medical doctors and CT technicians regarding treatment planning.• Assist in developing new treatment techniques.• Maintain required records, reports and files and collect necessary statistics.• Report all safety concerns, equipment-related issues and mishaps immediately to the HOD.• Participate in academic activities of the department and organization.• Be part of quality improvement initiatives and departmental protocols.• Carry out routine measurements and analysis of radiation and radioactivity levels in controlled and supervised areas.• Maintain records of radiation monitoring results.• Investigate situations that may lead to potential radiation exposure.• Advise the employer on regulatory compliance, radiation safety measures and radioactive material handling.• Recommend remedial actions for radiation-related incidents and exposures.• Ensure hazardous situations and corrective actions are reported to the competent authority.• Ensure quality assurance tests of structures, systems, components and sources are conducted.• Ensure monitoring instruments are calibrated periodically.• Train workers on radiation hazards, safety measures and safe work practices.• Ensure safe disposal of radioactive waste.• Develop emergency response plans and maintain emergency preparedness.• Advise the licensee regarding safety and security of radioactive sources.• Submit periodic radiation safety reports to the licensee and competent authority.• Inform the competent authority upon cessation of employment as RSO.Qualification & Experience• Work Experience 2–5 Years• Qualification M.Sc (Physics) & Diploma in Radiological Physics or M.Sc (Medical Physics)