Responsibilities To provide & ensure direct or indirect accurate medical attention to all cases before any surgical procedure. To practice evidence based medicine.To provide quality clinical care to patients.To ensure timely attention and intervention for any query or requirement from the IP patient.To ensure that IP rounds are duly done and the patients are attended empatheticallyTo ensure clear and prompt communication with the admitting as well as Referral Consultants.To complete all OP & IP records on time with accuracy.To take part in all regular CME’s.To ensure emergency preparedness & Response treatment /Procedure/Investigations.To ensure that ethical medical practice is followed.To Compliance with patient protocols(OPIP/OT/Diagnostics/ICU/Triage)To follow Infection Control protocols proper Bio Medical Waste Management.To document patient file/Prescriptions/requisitions (legible/complete).To ensure MLC notification/documentation and statutory compliance.To ensure Documentation at the time of Discharge.To be well groomed, punctual & adhere to company policies and practices.Qualification & Experience Minimum QualificationsMD/DNB/DA – Anesthesia/MEM/MD/DNB – Pulmonary MedicineExperience0-3 years of relevant experience in a renowned Hospital. Exposure to pain clinic & critical care will be an added advantage.

ResponsibilitiesTranscribe dictated Nuclear Medicine reports, including PET-CT, SPECT-CT, Bone Scan, Thyroid Scan, Renal Scan, Cardiac Nuclear Medicine, and radionuclide therapy reports. Edit and proofread reports generated through speech-recognition software for accuracy and completeness. Ensure correct usage of medical terminology, anatomy, physiology, radiopharmaceutical names, and nuclear medicine abbreviations. Verify patient demographics, clinical history, investigation details, and report formatting before final submission.Maintain turnaround time (TAT) as per departmental standards.Coordinate with Nuclear Medicine physicians regarding unclear dictations, missing information, or report corrections.

Qualification & Experience               Qualification- MBBS         Experience- 1- 2 yrs.                    

Qualification & Experience                Qualification- MBBS  Experience- 0- 2 yrs.  Requirement for RMO Ward  

Qualification & Experience            Department : Nephrology              Qualification : UG - MBBS, PG - General medicine, - DrNB - Nephrology                                              Experience : Fresher     Experience :In the department of Nephrology                      

ResponsibilitiesPrepare patients for PET-CT procedures and explain the scanning process.Verify patient identity, clinical history, and investigation requests.Administer radiopharmaceuticals as per physician instructions and protocols.Operate PET-CT equipment and acquire high-quality diagnostic images.Monitor patients before, during, and after procedures.Maintain radiation safety standards and infection control practices.Ensure proper handling, storage, and disposal of radioactive materials.Maintain accurate patient records and scan documentation.Coordinate with oncology consultants, radiologists, and nursing teams.Perform routine equipment quality control checks.Assist in scheduling and patient flow management.Qualification & Experience B.Sc./Diploma in Nuclear Medicine Technology, Radiology, or Medical Imaging Technology.Certification in PET-CT/Nuclear Medicine preferred.Knowledge of radiation safety regulations.

Qualification & ExperienceMBBS 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.

Qualification & Experience           Department : General Medicine            Qualification : UG - MBBS, PG - General medicine                                   Experience : Fresher             

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.  Experience in medical content writing /writing in academic settings/ communications experience within an agency, CRO, Pharma / Biotech Company.  Effective English verbal and written communication with flexibility to be clear, consistent, compliant, and appropriate for a variety of settings  Demonstrated ability to work effectively in a team and understand the applications of technology to medical content development  

ResponsibilitiesOverall responsibilities for quality assurance compliance at the Zydus Hospira Oncology Private Limited (ZHOPL) site and Pfizer Quality & ensure sustainable GMP compliance for Pfizer Products manufactured at ZHOPL site as per Quality agreement.Batch record review and release authorization compliance functions:Responsible for review and authorize the packed batch lot(s) for distribution in respective market from ZHOPL.To be part of SQRT as needed for any Batch related issue discussion.Regulatory impact assessment for all types of change related to Pfizer productsResponsible for Review and approval of Change controls at ZHOPL as per the Pfizer requirements.Responsible for performing the SCNM (Site Compliance Network Member) activities at ZHOPL and create the PAC and PCF in the PDM systems.Responsible for the review and approval of submission package as per procedure REG-459.Review BoH Queries & response and compendial/scientific data changesResponsible for review and approval for NPL assessment and dossier handover to ZHOPL  Qualification & ExperienceB. Pharm/ M. Pharm / M.Sc. with minimum 6+ years of experienceStrong understanding of Quality System functions, manufacturing and packaging processes, validations, batch documents , customer complaints, investigations, Training management, change controls, document Management.Ability to apply mathematical concepts, particularly statistics and probability, to Quality Engineering tasksExcellent technical writing, communication, and presentation skillsProficiency in Microsoft Office, Microsoft Project, and Statistical SoftwareExperience in preparing and participating in audits and inspections