Qualification & Experience Qualifications for Intensivist:MD (Medicine/Anesthesia/Chest medicine) Or Post Graduate Diploma in Anesthesia/Chest Medicine.Additional qualifications like FNB critical care medicine or Fellowship in critical care medicine or IDCCM or EDIC or MRCP or MRCEM will be preferred.Post PG at least 2 years of ICU experience.

Qualification & Experience Qualifications for ICU Registrar:MBBS with at least 2 years of ICU experience.Preference will be given to those with additional qualifications like CTCCM or Fellowship in critical care medicine.

ResponsibilitiesActive participation in the formulation of the philosophy of the school Planning implementation and evaluation of the curriculum Preparation of course outline and lesson plans of subject/subjects assigned Plan clinical rotation and clinical teaching Supervision of students in the clinical field/ Community Health Plan teaching/ demonstration, setting up of laboratory for the assigned subject Plan, construct, administer and evaluate tests/exams Prepare students for Council/Board exams Give and evaluate student assignments Participate in working of various committees Maintain all records pertaining to students and the School Guidance and counseling of students Plan and arrange external lectures, educational visits Plan and organize the Community Health field for both urban and rural areas Maintain and order supplies Participate in curricular, co-curricular and extra-curricular activities Participate actively in professional activities Any other duty that may be assigned from time to time Any other work/responsibility assigned by the HOD/Management in the course of business/work whether within the same unit/dept or any other unit/dept from time to timeQualification & Experience B.Sc. – Nursing P.B.B.Sc MSc. Nursing would be an added advantage0 – 2 years teaching experience in Nursing School

Qualification & Experience Qualification: MD/DNB – Emergency Medicine/Anesthesia/General Medicine/Critical CareExperience: 1 year to 7 years Interested candidates can send in their CVs to [email protected] or [email protected]

ResponsibilitiesConduct Clinical Marketing Education Programs, Live workshops , Seminars, Round Table Meetings, Promotional Events and In-service Programs ( ISPs) in the respective region in order to improve MDS -AAD value proposition amongst both clinical and economic buyers, by engaging KOLs towards MDS-AAD business outcome and achieve regional business objectives. Clinical capability building (administering trainings, continuous evaluation) amongst regional MDS -AAD direct selling organization and amongst channel partners in line with the country clinical objectives in order to enhance their ability to adequately differentiate the brand MDS -AAD in the market and thus achieve targeted business outcomes. Train HCPs on product use techniques through live workshops. Creating and implementing the regional calendar of engagements with the potential / existing customers in order to create strong brand awareness and creating door openers at the relevant levels. Support / assist sales organization with product evaluations, clinical audits in hospitals, setting protocols and processes in hospitals and 'critical to business' technical challenges (including but not limited to troubleshooting and product applications) in order to attain high levels of product penetration, query resolution and trouble free product application. Leading key customer relationship management and creation of regional KOL network in order to ensure usage of full array of MDS -AAD products. Coordinate on the timely completion of clinical /economic studies initiated in the region in order to ensure that the clinical / economic studies planned for the year are completed within the stipulated timelines. Conduct Induction Training Programs (Clinical & Product Training) to Sales Organization, provide clinical Updates, annual / quarterly Product refreshers and run Clinical Proficiency Tests on a need basis / from time to timeQualification & Experience Qualification: MBBS & MBA (Preferable) / Nursing Experience: 5-7 Years of Experience in Pharmaceutical / Healthcare Industry

ResponsibilitiesThe Associate Manager will develop with support and supervision, relevant medical affairs content, including abstracts, manuscripts, congress posters/presentations, graphical abstracts, systematic literature reviews, plain language summaries, slide decks, medical education resources, social media, infographics, video, multi-media and other types of external-facing medical content. Responsibilities may include researching, organizing, compiling, interpreting, and quality check of various types of technical and/or medical content. Provide solutions to stakeholders in alignment with manager for all projects and collaborate with other teams to drive these solutions (Graphics, Compliance agency, Statistics teams, etc.). Ensure execution of all projects within expected timelines while adhering to all quality and compliance requirements for medical content. Ensure training on relevant tools and processes, including new generative AI technology platforms, that ensure efficient and compliant execution of all medical affairs content. Track the progress of projects and resolve any issues/problems with guidance from manager. Identify and train to become an expert on one new tool/skill for content creation representing the latest trends in the industry. Qualification & ExperienceAdvanced scientific degree, (eg, MS, MRes, MPharm, PhD, PharmD, MBBS/MD) 2+ years experience in pharmaceutical medicine, including medical affairs, medical compliance. Proven ability to take ownership of individual work and align with more experienced colleagues on scope, timelines, quality expectations, etc. Strong interpersonal skills to quickly build rapport and credibility with colleagues and key external stakeholders cross culturally/regionally. 

ResponsibilitiesThe Manager will develop all relevant medical affairs content, including abstracts, manuscripts, congress posters/presentations, graphical abstracts, systematic literature reviews, plain language summaries, slide decks, medical education resources, social media, infographics, video, multi-media and other types of external-facing medical content. Development of drafts includes researching, organizing, compiling, interpreting and quality check of various types of technical and/or medical information for straightforward projects with internal review support. Collaborate with the support of a more experienced colleague with cross-functional partners including medical communications & content teams, scientific publication committee teams, congress working teams, digital channel content teams and generative AI working groups to develop medical content across assigned therapeutic areas/medicines. With the support of a more experienced colleague, provide solutions to authors for assigned projects and collaborate with other teams to drive these solutions (Graphics, Compliance agency, Statistics teams, Gen AI, etc.). Qualification & ExperienceAdvanced scientific doctoral degree, (eg, PhD, PharmD, MBBS/MD, MSc, MPH, MPharm) Excellent scientific writing skills, including an ability to interpret and summarize complicated data effectively, concisely, and persuasively. Minimum of 3 years of experience in writing/developing medical content for the pharmaceutical industry, academic settings, CRO, or biotech company

ResponsibilitiesProduction of radionuclides Preparation and testing of radiopharmaceuticals. Dispensing of radiopharmaceuticals Ensures compliance with all regulatory commitments including the cGMP, Radiation Safety, Pharmacy laws and corporate policies and procedures and other applicable Federal, State and Local authorities. Responsible and accountable under State Pharmacy Law, for all actions of personnel working in the permitted pharmacy area, in the absence of the Pharmacy Manager (PIC). Delivers and ensures performance of aseptic techniques, including sterility test and pyrogen testing per company standard operating procedures. Ensures performance of QC procedures using analytical equipment and chemical tests per company standard operating procedures. Maintains all applicable documents and records. Prepares shipment of radioactive materials according to procedure and licensing authorities requirements. Provides support in operation and maintenance of cyclotron, chemistry modules, QC equipment and associated softwareQualificationPharmacy License or ability to acquire license Bachelors Degree Communicates effectively with a proven ability to interpret information and provide and/or follow complex instructions. Ability to work independently and/or as part of a cross-functional team. Strong customer relations skills.

ResponsibilitiesDefine and evolve product strategy and roadmap for complex, distributed healthcare software platforms, ensuring alignment with customer needs, clinical workflows, interoperability requirements, and long?term business objectives. Collaborate cross?functionally with Engineering, Architecture, QA, Clinical, and Customer?facing teams to translate user needs and regulatory constraints into clear product requirements, epics, and prioritized backlogs. Drive requirements clarity and system definition, partnering with architects to shape interfaces, data flows, and integration strategies—especially across oncology, imaging, and hospital information systems. Ensure compliance with industry standards and regulatory expectations, embedding safety?critical considerations, quality processes, and interoperability standards such as FHIR, HL7, and DICOM into product decisions. Own cross?functional communication and alignment, coordinate with other product owners to align roadmaps providing clear articulation of product goals, tradeoffs, and outcomes to diverse stakeholders including executives, engineering teams, clinical partners, and customers.Qualification & Expeirence10+ Years of experience as a Product Manager. Master’s or Bachelor’s Degree in Computer Science, Engineering, Business, Healthcare Informatics, or related field—or equivalent experience with advanced applied work. Demonstratable experience in product management or related roles defining and delivering distributed software systems at scale, ideally within healthcare or other regulated domains.

Responsibilities Calibration of dose meters (including dosimetric inter-comparisons for QA) and radiation equipment (accelerator monitor unit calibration) Beam data acquisition for treatment planning  Preparation of data for treatment planning systems Development/improvement of dose measurement systems and protocols and software for dosimetry purposes (including spreadsheets and databases)  Ensures compliance with Federal, State and organizational regulations for radiation safety.  Participates in development of organizational Performance Improvement activities, policies and procedures, standards of practice to meet required regulatory requirements.  Assists in Acceptance testing and commissioning of new machines and acceptance testing and re-commissioning after major maintenance  Performs individual treatment planning, dosimetry calculations, and treatment planning reviews (physics component)  Provides physics consultation to all radiation oncology personnel and radiation oncologist concerning aspects of patient care and treatmentQualification & Experience M.S. or PhD (preferred) in Medical Physics, or a closely related field, required.  Position includes a single TrueBeam program supporting SBRT, HDR program, and a Gamma Knife program  Minimum of 3+ years clinical experience in addition to a CAMPEP-accredited residency.  Candidates who have passed the Part-I and (possibly) part-II ABR Exams preferred  Experience with High Dose Rate (HDR) and Stereotactic Radiosurgery (SRS) programs preferred.