ResponsibilitiesTo provide medical cover, routine and emergency, during hours of duty and work in conjunction with the other specialties / teams for ensuring patient care.Qualification & Experience0 - 5 Years experienceQualificationMBBS /MD/DNB (Medicine or Anaesthesia)/DA

ResponsibilitiesProfessional approach to be adapted with all patients, staff and visitors. To provide medical cover, routine and emergency, during hours of duty and work in conjunction with the other specialties to serve the institute. To be able to perform procedures like Central line, IV Channelization, Intubation etc. To be able to operate instruments like Ventilator. Following all Clinical safety, hygiene, infection control protocols (e.g. wearing gloves when required, aprons, maintaining hand hygiene, etc). To be available to monitor patients as and when required or when requested. Required to identify the complex health problems of the patients and report immediately to the concerned doctor. Supervise daily clinical management of all patients under the guidance of Consultants. Should be able to prescribe pain management medicines. Effective communication with patients, family, colleagues and other health care workers. Treatment sheets to be complete with diagnosis (capital letters). Each treatment sheet should be dated, named and signed by the writing doctor. Doctors should refer to the progress notes while writing treatment sheets. To assist the Consultants for rounds apart from taking independent rounds themselves and should follow up the patients for any further care (change in plan of Treatment). Required to accompany Consultants for rounds and taking notes as required Preparing the discharge summary. Being responsible for assessment of the new patients admitted. Required to follow the on-call and duty rota based on the department’s requirement. To be part of the Quality Improvement Initiative and protocols of the organization. Qualification & Experience2 - 5 YearsQualificationMBBS, MD/DNB (Emergency Medicine)

ResponsibilitiesTo attend any new patient (admission) within prescribed time frameTo examine & take a proper history of the patient (If he is in a position to give it on his own) or from his relative.Check any previous records, if available.Charts down all the details in the history sheet.Inform the respective consultant about the admission follow his orders.Instruct the nursing staff about the necessary orders to be carried out.If there’s a transfer in-patient from the ICU. Read the transfer summary/ clinical notes carefully and act accordingly.Inform the respective consultants whenever seems significant.Shift Duty:To take rounds and examine individual patients at least once in every shift and as & when needed. Inform the respective consultant/ Registrars if any new findings.To put the notes in clinical sheet.To enter the relevant details of each and every patient accordingly.Attend rounds with the respective consultants and carry out the necessary changes in the order. Enter them in the treatment sheet.Fill the Medicine Card and Non Drug Order sheetTo instruct the nursing staff about orders and follow them upTo follow up with all the investigations to be seen and trace their results. Note down investigation results in the investigation sheet.To Document Verbal Orders correctly in clinical notes if given by consultants.To respond to emergency calls and to activate code blue if any medical emergency is encountered beyond your control.To identify the critical status of patient and shift him to critical care area in time.Always contact primary consultant if found necessary at any point of time.Discharges:Prepare discharge summaries well in advance according to the policy.Pre Surgical & Post Surgical Patients:To follow pre-operative orders in the treatment sheet. To check whether the consents (Surgical, Anesthesia, etc) for the surgery has been taken from the patient. If not inform the respective person.To get the PAC done. To carry out all the pre-operative orders.Inform the consultant over phone during night shift about patient status who are scheduled for surgery next day.To attend patients complaints. To calm the patients if they are apprehensive. Inform the consultant if needed.General:To attend camps according to the policy.To work as per Policies and procedures of organization.To get the cross referral form filled abd call cross consultants according to the policy.Use capital letters for medicines (Generic Names/ Salt) and always put sign, name, date and time with every entry you make.To take care about completeness of records To act accordingly as per communicated by hospital management team.Skill Sets:Verbal Ability/Communication Skill: Ability to comprehend verbal instructions given by the supervisor or head of the department.To give accurate and tactful explanations to patients. Problem solving/ Decision-makingTo think independently and exercise own judgment in consensus with the supervisor.Qualification & Experience Able to work accurately and with minimal supervision.Ability to comprehend written instructions given by the Doctors and the other related departmental personnel.Ability to plan & organize ones work schedule effectively.Speaking and listening are essential requirements to understand and carry out the instructions given by the supervisors and other related departmental personnel.Affinity to work in team.Verbal Ability/Communication Skill: Ability to comprehend verbal instructions given by the supervisor or head of the department.To give accurate and tactful explanations to patients. Problem solving/ Decision-makingTo think independently and exercise own judgment in consensus with the supervisor.Enthusiasm.Open-mindedness.

Qualification & Experience           MBBS / BHMS / BAMS         Fresher’s & Experience in ICU/Ward preferred                        

Qualification & Experience          Department Reproductive Medicine               Qualification MS/DNB/Fellowship in Reproductive Medicine with 3 -5 years experience                        

Responsibilities• You will be responsible for the engagement of identified key thought leaders through medical affairs activities, in alignment with the overall strategic plan?• You will be responsible to execution of strategic medical affairs plan including but not limited to medical education, product education, medical evidence generation, advisory boards, pre-license activities and special projects??• You will be a therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, patients’ treatment trends and studies in the therapeutic areas in which the Company is?? involved, with defined audience of leading specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other Stakeholders) and to be considered a trusted scientific counterpart?• You will be responsible with therapy area lead to support optimal patient outcomes through communication of data, information, knowledge and insights in support of healthcare professional needs and organizational goals??• You will have to represent the organization in various internal & external scientific platforms??• You will have to gather deep insights on disease trends and treatment patterns from key thought leaders and conveying them back to the therapy lead and commercial teams.??• You will need to proactively conduct disease trend analysis in identified disease segments and contribute effectively to the development of annual Medical Affairs Strategy Plan?• You will be receiving and processing scientific information requests received from physicians?• You will have to ensure that all activities in the region are conducted in alignment to organisation’s COBE (Code of Business Ethics) Policy and compliance guidelines.• You will need to collaborate with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in reputed journals.• You will be responsible for devising an optimal training plan to ensure the flow of the latest medical developments to the sales and marketing teams.• You will jointly be responsible with the therapy area lead to support optimal patient outcomes through communication of data, information, knowledge, and insights in support of healthcare professional needs and organizational goals.• Representing the organization in various internal and external scientific platforms will be among your responsibilities.• You will be responsible for developing the Medical Affairs strategic plan for identified therapeutic areas and products.• Your ability to convert insights on disease trends and treatment patterns from key thought leaders into viable and formidable strategic plans to shape the therapeutic areas of interest will be vital.• You will be responsible for identifying knowledge gaps, practice gaps, and data gaps and developing strategic medical action plans, including but not limited to medical education, product education, evidence generation, and special projects, will fall under your responsibility.• Collaborating with thought leaders to conduct therapy-specific reviews, meta-analysis, case studies, case series, patient-reported outcomes, and publishing them in reputable journals will be part of your role.• Handling complex questions from healthcare professionals related to GGI products or disease areas to satisfaction will be a key responsibility.• You will be responsible for ensuring that all activities in the therapeutic area are conducted in alignment with Dr. Reddy's COBE (Code of Business Ethics) Policy and compliance guidelines will be essential.• You will be responsible for ensuring that all promotional, physician, and patient education materials are approved within stipulated timelines and in alignment with Dr. Reddy's Promotional Material approval policy.• As a product pipeline champion, you will have the ability to identify unmet needs through active stakeholder interactions and actively contribute to the new product ideation and development of differentiated products. Qualification & Experience• Educational Qualification- MBBS with full time post-graduate qualification of at least 2-years’ duration in any discipline of medicine/ M.B.B.S with M.B.A. from a reputed institute • Minimum work experience- Fresh postgraduate or up to 2 years of experience in Field based Medical Affairs.• Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data?• Experience with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer relationship?• Experience with complex business environments preferred?• Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards.

ResponsibilitiesPreparation, review and approval of of Standard Operating Procedures (SOPs).Preparation, review and approval of various protocols and reports, including:Confirmatory Batch ProtocolHold Time ProtocolProcess Evaluation (Pre-validation) ProtocolTrial ProtocolProcess Performance Qualification/Validation ProtocolStability ProtocolPreparation of Master Production Records (MPRs) such as:Master Formula Record (MFR)Manufacturing Instructions (MI)Production Order Raw Materials (PORM)Good process knowledge of OSD and semi solids processes.Good Expert in MES - PASIX Design and troubleshooting Designing of Master Batch Records (MBRs) in PASIX, ESP, GMBR, PVL, and PMBR based on MPR/PIS/MPC for new products as well as site transfer products, following SOPs and GMP requirements.Document circulation to cross-functional teams (CFT), follow-up for review, corrections, and approval.Creation and modification of Bill of Materials (BOM) and Recipes in SAP.Follow-up for BOM and Recipe-related tasks for Exhibit, Validation, and Commercial products.Creation of codes in SAP, such as:Coated, Core, Blend, Enteric, Sub Coating and Drug LoadingCreation of reservations in SAP.Inter and intra communication for sending BOM messages to CFTs. Qualification & ExperienceB.Pharm/M.Pharm/M.ScMES Design Exposure good to have

Qualification & Experience                MBBS/BHMS/BAMS with experience or Freshers.                   Experience or Freshers           

Qualification & Experience                                       MBBS / BHMS / BAMS                                          

Qualification & Experience           Qualifications: Fellowship in Fetal Medicine                  Experience : 3 years