ResponsibilitiesClinical Competency FrameworkCognitive Clinical Management(Clinical reasoning, decision-making, and documentation)Perform and document history & physical examinationFormulate differential diagnosisDevelop and document initial plan of careWrite daily progress notesInterpret laboratory and radiological resultsInterpret hemodynamic parameters in critically ill patientsPrepare discharge summaryClinical Non-Invasive Management(Patient care without procedural intervention)Order appropriate investigationsOrder appropriate medications and treatment plansOrder referrals to other specialtiesManage blood transfusions and blood productsArrange and adjust artificial feeding modalitiesPerform preoperative workupObtain and document informed consentClinical Invasive Management(Procedural and surgical skills)Perform nasogastric intubationInsert urethral catheterPerform surgical procedures under consultant supervisionAssist in / perform re-exploration surgeriesAcademic & Professional ResponsibilitiesParticipate in teaching activities (intradepartmental & interdepartmental)Engage in clinical discussions, case presentations, and auditsDocumentation & Patient Safety (Cross-cutting domain)These apply across all categories:Accurate clinical documentationEthical practice including informed consentSafe prescribing and monitoringCoordination of continuity of care

ResponsibilitiesTo Provide Quality clinical Care to surgical PatientsTo ensure timely attention and intervention for any query or requirement from the IP surgical patient. To ensure Emergency Preparedness & Response Treatment/ Procedure/ Investigations)To ensure that the surgical IP rounds are duly done and the patients are attended empatheticallyTo practice evidence based treatment regarding patient {Investigation-(profile/reports/plan)}-{Treatment- (details/drug procurement)} {Drug Allergies/ patient history}.To Compliance with patient protocols (OP-IP/OT/ Diagnostics/ ICU/ Triage)To Document patient File/ Prescriptions/requisitions (legible/ complete)To ensure Documentation at the time of DischargeTo workup of all IP patients for surgery & ensure tie-up preparation consent.To ensure adequate care of all part up cases.To complete all OP & IP records on time with accuracy. To ensure on-time availability of technical equipment for surgery and assist all surgical consultants in O.T. procedures To have complete orientation of QMS and EMS system of Hospital. To have complete Awareness about Disaster Management Programme (DMP) of the hospital.To Comply with the service quality Process, environmental & occupational issues & policies of the respective areaTo Comply with patient safety policyTo ensure safe utilization of equipments and proper waste disposal system. To ensure that ethical Medical practice is followed. To ensure clear and prompt communication with the admitting as well as Referral consultants.Qualification & ExperienceMinimum QualificationsMBBS; M.S. / DNB (MCh/ DNB/ FNB- As required)ExperienceMin 3 years (post MS/ DNB) & 0-2 years (post MCh/DNB/ FNB)

Qualification & ExperienceDepartment: NURSING (ICU/ CCU/ SICU/ DIALYSIS/ EMERGENCY/ CTVS/ OT/LR)Designation: SR. NURSING OFFICERS/ NURSING OFFICERSQualification: B.SC- NURSING/ GNMExperience: RELEVANT EXP OF MIN 5 YRS. IN RESPECTIVE DEPT.

Qualification & ExperienceDepartment: BIO-MEDICAL ENGINEERINGDesignation: MANAGER/ SR.MANAGERQualification: B.TECH/B.E .- BIOMEDICAL ENGINEERING/MEDICAL ELECTRONICS/ ELECTRONICS & COMMUNICATIONExperience: MINIMUM 10 YRS. IN A MULTI/SUPER-SPECIALITY HOSPITAL OF REPUTE IN DELHI/NCR

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

Qualification & ExperienceMD / DNB / DA AnesthesiaMMC registration mandatory2-5 years of post-qualification experience preferredExperience in ICU, emergency, and OT anesthesia management preferredExperience 2-5 Years

Qualification & ExperienceDepartment : Physicial Medicine & RehabilitationMasters/Bachelors in Occupational Therapy with AIOTA RegistrationExperience 0-4 Years

ResponsibilitiesDevelop, document, and maintain end?to?end regulatory strategies for medical devices across the key markets, ensuring alignment with product technology, intended use, risk classification, and business objectives. Manage preparation, review, and submission of regulatory dossiers, including: 510(k), PMA, Medical Device License applications, CE marking submissions, Investigational Device Exemptions (IDE), Humanitarian Device Exemptions (HDE) submissions ensuring accuracy, consistency, and regulatory compliance of all submissions. Maintain the dossiers by filing annual reports and manage post?approval submissions and Lead change impact assessments for Design modifications, Manufacturing and process changes, Supplier and raw material changes, labeling changes by accurately assessing and classifying the changes and prepare and manage change submissions and notifications to agencies. Provide regulatory input on Human factors and usability engineering and assess regulatory adequacy of design and development documentation, Device verification and validation etc. Review and assess preclinical testing data (bench, biocompatibility, electrical safety, EMC, etc.), Clinical investigation data and performance evidence and ensure clinical and preclinical data meet regional regulatory expectations and are appropriately aligned with device claims and intended use. Manage activities related to supplier qualification, CAPAs, complaint handling, product performance and audits Act as a regulatory point of contact and prepare and coordinate responses to regulatory authority questions, deficiencies, and follow?ups, with agencies Develop and execute engagement strategies with agencies, including Pre?Submission meetings, key regulatory questions, and incorporation of agency feedback into development and submission plans. Act as the regulatory strategy lead on cross?functional project teams, translating complex regulatory requirements into actionable development and execution plans. Communicate clearly (written and oral) internally (e.g., company personnel) and externally (e.g., regulatory agencies, auditors, vendors)Qualification & ExperienceBachelor’s degree in Life Sciences, Engineering, Biomedical Sciences, or related field Advanced technical degree (PhD, MBA) preferred Experience More than 15 years of progressive medical device regulatory experience Hands?on experience with: FDA submissions (510(k), PMA, IDE) EU MDR and CE marking Health Canada device licensing

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.

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.