ResponsibilitiesConsult with patients to determine their health concerns and conditions.Evaluating patients who may need surgical or non-surgical treatment for conditions related to the ear, nose, and throat, and related structuresPerforming comprehensive examinations of the ear, nose, and throat, and other head and neck structures to diagnose illnesses, injuries, or disordersInterpreting results from diagnostic tests, such as audiograms (hearing tests), and imaging studiesAdvising patients on their condition, possible treatment options, and preventative measures.Prescribe medication to treat various conditions.Planning and carrying out medical and surgical treatments, including but not limited to tonsillectomies, adenoidectomies, myringotomies, and sinus surgeriesCoordinating with other healthcare professionals for the management of patients’ health problemsDocumenting patient care by maintaining detailed notes of appointments and treatment plansStaying informed about latest developments in otolaryngology and participating in continuing education activitiesPracticing health and safety standards to ensure a sanitary and safe environment for patientsQualification & Experience Affinity to work in a team.Enthusiasm.Open-mindedness.

ResponsibilitiesAdmission, discharge & transfer of patients.Data collection.Assessment of vital sigh.Physical examination & diagnostic evaluation.Continuous monitoring of patient.Following physical round & carrying out the order prescribed.Sending sample for diagnostic evaluations per requirement.Coordinating diagnostic & therapeutic procedure.Planning & implementation of patient care includes hygiene & nutrition.Administering medication.Providing comfort measures.Taking care of elimination.Giving health education.Maintaining records & reports.Attaining in-service education.

ResponsibilitiesLead end-to-end regulatory activities for innovative biological product portfolios across global markets (Emerging Markets).Develop and execute regulatory strategies aligned with business objectives and market requirements.Oversee preparation, review, and submission of dossiers (CTD/eCTD) including IND/IMPD/CTA, MAA, variations, amendments, and renewals.Act as the primary point of contact with country affiliates and global health authorities for regulatory interactions, queries, and inspections.Provide strategic guidance on regulatory pathways for biological products including clinical requirements of country of origin or single region clinical study data.Ensure compliance with evolving regulatory frameworks, guidelines, and quality standards.Collaborate with partners and cross-functional teams (R&D, Quality, Clinical, Medical, Manufacturing, commercial, marketing and supply Chain) to drive regulatory milestones.Identify risks in submission timelines and proactively implement mitigation plans.Qualification & Experience Advanced degree in Pharmacy, Biotechnology, or related field.Strong experience in Regulatory Affairs with exposure to biosimilars or biologicals.Proven experience in handling global submissions (ANVISA, SAHPRA, DIGIMED, TGA, MEDSAFE, COFEPRESS,USFDA, EMA, or other major agencies).Strong understanding of biosimilar regulatory frameworks and lifecycle management.Excellent communication, strategic thinking, and stakeholder management skills.Regulatory Strategy & ComplianceGlobal Stakeholder ManagementAnalytical & Problem-Solving SkillsStrong Execution & OwnershipEducational qualification: Post graduate in Pharmacy/ScienceMinimum work experience: 8+ years in Pharmaceutical Industry with 5 years of experience in global regulatory affairs.Experience in formulation development, analytical development and quality.Understanding of Good Manufacturing practice/Quality Systems.Understanding of product development, manufacturing processes, Intellectual Property and quality.Technical knowledge and understanding of the regulatory requirements of different dosage forms.Thorough understanding of regulatory guidelines for different countries, ICH guidelines, pharmacopeia's, product filing and approval requirements.

ResponsibilitiesApplies knowledge and skills relevant to Disinfection and Sterilization Infection Control Guidelines to the management of the sterilization services at the HospitalPlans, prioritizes and processes the required instrumentation to enable the operating theatres and other services to run efficiently on a daily basisPerform all daily validation requirements and ensure record keeping and tracking are documented and stored appropriatelyMaintains sterile stock levels for the operating theatres to function on a daily basis for planned activityAssesses staff for on-going education and up skilling within the roles of the sterilization departmentDevelopment of competencies and policies to ensure all staff working within the sterilization department are confident in their rolesMaintains safe practices and working environment in accordance with the hospital policy and procedure as varied from time to timeAccept responsibility for own professional developmentPrioritizes purchasing of replacement instrumentation and liaises with company representatives to ensure all is in safe working order for the unitsShould know precautions for safe use and handling of sterilizer (Steam & E.T.O).Drain the water in heater’s chamber after finishing all cycles daily.Before starting the cycle check the water level (RO water) in machine.Before starting the machine (Steam & E.T.O) read all the instruction without fail.Read and follow the Log-Book.Maintaining the following registers:Shift relieving registerMachine Operating register. (Steam & E.T.O)Incident Report register.Re-call Register.Material Receiving and Issuing register.

ResponsibilitiesPerform CT Scan and MRI procedures as prescribed by radiologists and physicians.Prepare patients for imaging procedures by explaining protocols and ensuring patient comfort and safety.Operate and maintain CT and MRI equipment efficiently and safely.Administer contrast media under radiologist supervision and monitor patients for adverse reactions.Ensure accurate patient positioning and image acquisition for optimal diagnostic quality.Monitor radiation safety measures and MRI safety protocols at all times.Assist radiologists during specialized imaging procedures and emergency cases.Review imaging results for clarity and completeness before submission to radiologists.Maintain imaging records, patient data, and procedure documentation accurately.Troubleshoot minor equipment issues and coordinate maintenance/service requirements.Ensure proper sterilization, infection control, and biomedical waste management practices.Train and supervise junior technicians, interns, and support staff.Coordinate scheduling and workflow to ensure timely imaging services.Maintain adequate stock of contrast agents, consumables, and emergency supplies.Participate in quality assurance and accreditation activities within the department.Qualification & Experience Diploma / Bachelor’s Degree in Radiology Imaging Technology or Medical Imaging Technology.Certification in CT & MRI Technology preferred.Valid radiation safety certification as per regulatory requirements.

ResponsibilitiesCoordinate VIP patient appointments, admissions, consultations, and discharge processesProvide personalized assistance and support to VIP patients and their attendantsEnsure smooth communication between patients, doctors, nursing staff, and hospital departmentsHandle special requests and prioritize patient comfort and satisfactionMonitor patient experiences and address concerns or escalations promptlyMaintain confidentiality and accurate patient recordsCoordinate diagnostic tests, billing support, and follow-up appointmentsAssist in managing guest relations and hospitality services within the hospitalEnsure adherence to hospital protocols and service standardsSupport hospital management in enhancing patient satisfaction initiativesQualification & Experience Any Graduate; Hospital Administration or Hospitality qualification preferred1–5 years of experience in patient coordination, guest relations, or hospital front officeExcellent communication and interpersonal skillsStrong coordination and problem-solving abilitiesAbility to handle patients professionally and empatheticallyBasic computer knowledge and documentation skillsKnowledge of hospital operations and patient service standards is an added advantage

Responsibilities               Assist in the preparation and submission of regulatory documents to health authorities for product registrations, including ANDAs/MAA/DCP/ANDS etc but not limited to these.Periodic tracking of evolving Global Regulatory updates and updating to team and implimentation of the new expectations of Global competent Regulatory Agencies and review of all relevant data inclusive of the Type II DMF/ASMF etc.Support the maintenance of regulatory files and databases, PLCM, ensuring accuracy and completeness of documentation.Collaborate with cross-functional teams, including Quality Assurance, R&D, and Manufacturing, to gather necessary information for regulatory submissions.Assist in the review of labeling and promotional materials to ensure compliance with regulatory standards.Participate in regulatory intelligence activities, including monitoring regulatory updates and communicating relevant information to internal stakeholders.Provide administrative support as needed, including organizing meetings, preparing meeting agendas, and documenting meeting minutes.Any other related duties as assigned by Project Leader                                            Qualification & Experience Currently enrolled in Master of Pharmacy degree program in Pharmacy, Regulatory Affairs, Life Sciences, or a related field.Strong attention to detail and organizational skills.Excellent written and verbal communication skills.Ability to work independently and collaboratively in a fast-paced environment.Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).Prior experience or coursework in regulatory affairs or the pharmaceutical industry is preferred.

Responsibilities               New Projects has been added in my group to handle that projects these man power is required.                                                          Qualification & Experience M. Pharma or M.Sc.   

Responsibilities               Be a Subject Matter Expert in method development of HPLC and GC techniques.                                      Basic instrument operational skills.                                                 Qualification & Experience M .Pharm .        

Qualification & Experience                                                 Department : Paediatrics          Qualification : UG - MBBS, PG - Paediatrics