Aster DM HealthCare Global Centre is looking for Staff Nurse to join our dynamic team and embark on a rewarding career journey. Provide high-quality patient care. Assist with the continuous development of staff. Identify hazards in the workplace and provide solutions. Treat emergency injuries. Develop programs to maintain health and safety. Identify work-related risks. Document all injuries and illnesses.

Aster DM HealthCare Global Centre is looking for Specialist to join our dynamic team and embark on a rewarding career journey. Diagnosing and treating illnesses, medical conditions, and injuries. Ordering, performing, and interpreting diagnostic tests. Collecting, recording, and maintaining patients' information and histories. Prescribing and administering treatments, therapies, medications, vaccinations, and other specialized medical care. Explaining procedures and discussing test results or prescribed treatments with patients and family members. Monitoring patients' conditions and progress. Directing, coordinating, consulting with, and referring patients to nurses, students, assistants, specialists, therapists, and other medical staff. Advising patients, parents, and guardians on diets, activities, hygiene, and disease prevention. Conducting research and remaining up to date on current trends, discoveries, and developments in the field

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines. Our 109,000 colleagues serve people in more than 160 countries. CORE JOB RESPONSIBILITIES REQUIRED Business generation & development: Achieve monthly, quarterly, half yearly and yearly sales target by promoting companys products ethically to customers as per the business plan, also ensure Doctor / Customer Call average as per the customer management plan of the division Organizing Camps (CME) as per the division strategy and customer needs Facilitate the process of successful new product launch. To create and update customer list as per the therapy and product of the division. Ensure Ipad adoption (if applicable) as per division norms and adherence to CLM calls Brand Management: Prescription audit for Abbott brands and other competitors brands Generate POBs for Abbott brands as per the business plan REQUIRED EXPERIENCE BSc/ B. Pharm or Any Graduate with minimum 2 years of prior experience as a Medical Representative PREFERRED EXPERIENCE Candidate with prior/current experience in the same therapy. Candidates from MNC and top Indian Pharma companies will have added advantages. Fluent and confident in communication LOCATION: India > Mumbai : BKC Building t

As a Therapy Business Manager you will be responsible for the development and performance of all sales strategies in assigned market. Further you will drive primary sales, secondary sales and ensuring brand presence in defined markets. You will supervise/manage the distributor network to achieve desired sales objectives thereby ensuring achievement of financial and ethical objectives of the division as per the business strategy. To achieve this you will have authority to develop your customer management plan, approve expiry products issue credit note for distributors under your control, recommending appointment and credit limits of distributors, develop, execute & plan your resource utilization and participate in Strategy Execution review meetings to ensure alignment. You have a very important role to play in Divisions success. Roles and Responsibilities in detail Territory Business Planning: Plan for the monthly and quarterly business. Plan demand generation and fulfillment Monitor actual Sales and mid-course corrections and inputs to reduce variance against expectations Prescription audit for Abbott brands and other competitors brands To create and update customer list having specified number of doctors /chemist (Trade) as per the therapy /product requirement and maintain the same in physical/electronic format. Business generation & development: Achieve monthly, quarterly, half-yearly, and yearly Sales targets by promoting companies products ethically to customers as per the business plan Having science base discussions with doctor and chemist for promotion of the product in the clinic and at the chemist place Organizing Camps (CME) as per the division strategy and customers need Execute the customer management plan to ensure that all the customers are covered as per the plan. Lead and execute strict adherence to Abbott Code of Business conduct Set examples on implementation of the code of business conduct, RCPA, Pharmacovigilance to ensure compliance Demonstrate and promote professional behavior in line with Abbott Values of Pioneering, Achieving, Caring, and Enduring Ensure a high level of customer service and manage any difficult customer situations. Division and business strategy will be shared with you on time to time base which you will have to execute to the fullest To attend and participate in Strategy meetings, briefing sessions, doctors meets, workshops, training programs, and any other programs undertaken by the company to equip you or activities for the performance of your job or promote the sales of products of the company or to improve company image. Meet minimum KPIs as follows: 100% coverage of Doctors. Customer Call average as per the customer management plan of the division /therapy. Market intelligence collection, retailer level inventory management calls as per the product profile and marketing strategy of the therapy /division. Experience/Training Required 2+ Years of experience. Candidate with prior/current experience in the same therapy. Candidates from MNC and top Indian Pharma companies will have added advantages. Fluent and confident in communication. LOCATION: India > Mumbai : BKC Building t

Senior Specialist, Medical Advisor Oncology The Senior Specialist Oncology will be responsible for providing strategic support and expertise in oncology to drive the development and implementation of medical affairs initiatives. This key role will involve collaborating with cross-functional teams, including clinical development, marketing, and regulatory affairs, to ensure the successful launch of oncology pipeline. The Senior Specialist Oncology will also be responsible for building and maintaining relationships with key opinion leaders (KOLs), lead data generation initiatives, participating in scientific conferences, and contributing to the overall medical affairs strategy. Key Responsibilities: People Manager Role - Senior Specialist Oncologist will manage 2 field-based medical advisors focusing on West and South region of India. Provide strategic guidance and expertise in oncology for the development and execution of medical affairs plans focusing on Lung Cancer, GU Cancers and Hematology portfolio Collaborate with cross-functional teams to support the successful launch and commercialization of oncology products. Serve as a subject matter expert in oncology for internal teams, including clinical development, marketing, and regulatory affairs. Build and maintain strong relationships with key opinion leaders (KOLs) in the oncology field. Stay up-to-date with the latest scientific advancements, clinical trial data, and competitive landscape in oncology. Contribute to the development of scientific communications, including publications, presentations, and educational materials. Represent the company at scientific conferences, symposiums, and advisory boards. Provide support and training to the sales and marketing teams on oncology products and disease management. Collaborate with external stakeholders, including healthcare professionals, patient advocacy groups, and professional organizations. Ensure compliance with all applicable regulations and guidelines, including pharmacovigilance reporting and medical information requests. We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we follow the science that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe. Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry professionals ensuring the scientific value of our products is realized. We engage and train internal employees to ensure that they thoroughly comprehend the science behind the medicine and review further unmet medical needs to bolster collaboration and further differentiate our portfolio. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Not Applicable Shift: Valid Driving License: Hazardous Material(s): Job Posting End Date: 04/15/2025 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Interested candidates share your resume to sanjay.behera@thyrocare.com or whatsapp to 8928285213 Key Responsibilities: Sample Preparation and Handling: Prepare and process samples (e.g., liquids, solids, environmental samples) for ICPMS and LCMS analysis. Prepare standards, reagents, and calibration solutions as needed for ICPMS and LCMS analyses. Ensure accurate and thorough labeling, storage, and disposal of samples, chemicals, and waste in compliance with safety regulations. ICPMS & LCMS Operation: Operate, calibrate, and maintain ICPMS and LCMS systems, ensuring high-quality data output. Perform routine analyses using ICPMS and LCMS techniques for the detection of metals, ions, and compounds in a variety of sample types. Prepare and run samples using ICPMS and LCMS, ensuring accuracy, precision, and efficiency. Troubleshoot instrument-related issues, optimizing performance as needed. Data Analysis and Reporting: Analyze data generated from ICPMS and LCMS instruments, ensuring accuracy and completeness of results. Interpret complex analytical data and compile reports for review by senior laboratory staff or clients. Document and track results in laboratory information management systems (LIMS) or appropriate software. Quality Control and Compliance: Ensure quality control standards are maintained throughout testing, including calibration, validation, and cross-checking results. Follow established laboratory protocols and regulatory guidelines (e.g., GLP, ISO standards) to ensure accurate and reliable data. Maintain and manage calibration standards, quality control samples, and blank samples to meet the required analytical accuracy. Instrumentation Maintenance and Troubleshooting: Conduct routine maintenance and calibration of ICPMS and LCMS instruments, ensuring they are functioning optimally. Troubleshoot and resolve instrument issues, collaborating with engineers or senior lab staff when necessary. Monitor instrument performance, ensuring that diagnostic or preventative maintenance is conducted according to schedules.

Roles and Responsibilities Provide high-quality patient care to pediatric patients in NICU, PICU, and pediatrics departments. Participate in quality improvement initiatives to enhance patient outcomes and hospital processes. Desired Candidate Profile MD Pediatrics degree from a recognized institution (DNB preferred). Excellent communication skills for effective interaction with patients' families. Ability to work flexibly under pressure during emergency situations.

SUMMARY Job Title: Process Executive Location: PAN India Eligibility Criteria: MBBS (Bachelor of Medicine, Bachelor of Surgery) Other eligible qualifications include Nursing, BDS, PharmD, BHMS, BAMS, BUMS, BYNS, B.V.Sc & AH, Bachelor of Occupational Therapy, Bachelor of Science in Biotechnology, Bachelor of Technology in Biomedical Engineering, Bachelor of Science in Microbiology (Non-Clinical), Bachelor of Science in Cardiac or Cardiovascular Technology, Bachelor of Perfusion Technology, Bachelor of Respiratory Therapy, Bachelor of Science in Nutrition and Dietetics, Bachelor of Science in Genetics, and related fields. Key Responsibilities: Engage in limited customer interaction with guidance. Comprehend domain processes, functions, and terminologies (e.g., SOP, QC checklists). Enter information from source documents into clinical/safety databases, ensuring accuracy and meeting deadlines. Handle critical or sensitive transactions as necessary. Code activities on assigned projects within specified timelines and with efficiency. Import uncoded terms into databases and export coded medical terms from coding platforms. Requirements Requirements: Strong understanding of medical terminology and coding practices. Excellent attention to detail and accuracy. Ability to work efficiently within specified timelines. Good communication and interpersonal skills.

1. To attend to patient complaints, queries related to the treatment and inform the on call RMOs/registrars/Consultants 2. To educate and counsel patient on the treatment whenever required. 3. To ensure the completeness of discharge summaries on time and get it verified from the registrar/consultant 4. To trace the investigation reports and update the tracker. 5. To inform panic value reports and ensure action taken. 6. To ensure completeness of consent and medication reconciliation forms. 7. To fill the TPA and any other forms required for insurance purpose 8. To book the appointments with other centers for any investigations if required. 9. To keep a record of all the admissions, discharges, sentinel events, code blues and update the medical services every day. 10. To ensure the nursing staff follow the required orders 11. To attend patients calls and inform on call Rmos / Registrars/ consultants. 12. To coordinate with the other supportive departments like CT scan, Radiology, blood bank, laboratory. 13. To ensure completeness of documentation. 14. To inform the referral doctors as per advised by Consultants. 15. To facilitate the discharge process 16. To conduct periodic audits for compliance to documentation as and when required by the Medical services 17. To keep a record of all the admissions, discharges, sentinel events, code blues and update the medical services every day.

Cardiac CT Technician

The Position Country Medical Director, India A healthier future. It s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That s what makes us Roche. As a Country Medical Director, you will drive scientific, medical and clinical excellence and innovation through strategic leadership, strong cross-functional interactions and continuous engagement with the scientific community and key health care ecosystem stakeholders. This leads to accelerated adoption of Roche s transformative medicines as standard of care. You will ensure medical compliance and superior patient outcomes while fostering a high performance culture and continuous professional development of the Medical team. You will be part of the affiliate s leadership team. Your Opportunity Strategic Leadership As part of the affiliate leadership team the CMD has a shared responsibility for the affiliate enterprise strategy, short, mid and long term outcomes with an E2E perspective, prioritization and adequate resourcing as well as impactful delivery of the agreed business objectives Ensure business success through competitive medical strategies built from fit for purpose evidence generation, value demonstration, scientific data positioning and dissemination whilst maintaining integrity and preserve the company s reputation Represent Roche and our scientific positions and portfolio as appropriate among key external stakeholders eg. eco-system representatives including politicians, policy makers, scientific partnerships, media interactions, patient advocacy, other pharma companies (individual or association). It is understood that for selected key customers the CMD serves as the primary point of contact with the ambition to drive positive healthcare system changes and where feasible earlier adoption of our transformative medicines Act as a role model mastering our VACC framework and ensure medical team members work effectively cross-functional for the benefit of the pipeline and on-market portfolio centered on patients and anchored in our innovation science Establish and maintain highest medical and scientific rigor in all areas, particularly in our current 5 Therapeutic Areas and 11 Diseases with E2E leadership Build scientifically sound medical teams capable of making portfolio differentiating decisions that translate into clinical practice adoption and broad access to our portfolio in full alignment with country opportunities and challenges Ensure medical and scientific contribution to the development of competitive and differentiating local and global strategies and appropriate locally adapted execution of tactics across the entire life cycle of our portfolio - overall balancing rigor and speed Enhance local and cross-country scientific activities to accelerate advocacy, community engagement, clinical adoption and access to our portfolio Support and foster integrated Outcome-based customer experience based on customers needs informing scientific and medical interventions that catalyze clinical practice adoption and advocacy Ensure timely and qualified input to inform and shape global asset and disease strategies including the integrated evidence plans to maximize the value demonstration of our assets across the life cycle, which requires adequate staffing for timely execution and preparation locally and ensure that learning and materials are passed on to subsequent launch wave countries License to Operate Champion Assurance of medical compliance as the local delegate of authority of Roche`s Pharma CMO Accountable for for purpose cross-functional teams Accountable for the appropriate approval process of non-promotional and promotional materials ensuring compliance with applicable local and global requirements. Accountable for the strategic and appropriate provision of medical Grants, Sponsorships and Donations. Developing Digital Health solutions locally has high complexity and compliance risks, thus, the CMD is accountable to ensure adherence to quality standards, rules and regulations. Ensures considerations of the risks, the portfolio fit and/or desired return of investment rests with the affiliate leadership team Who you are Attained MBBS, MD or PhD in the relevant area of study with significant experience in the pharmaceutical industry (15+ years) in a range of leadership and medical roles, with at least 5+ yrs in a leadership position Have a strong understanding of pharmaceutical business with profound Medical Affairs experience including medical scientific and strategic aspects of drug development and commercialization and Medical Compliance including experience and knowledge on GCP, GVP, Medical Device regulations and Healthcare Compliance Worked in a senior management function and has cross functional domain expertise Possess strong scientific acumen and should be respected externally as a scientific thought leader Ability to lead teams in an agile way and creating a working culture that is transparent and values driven and ensures personal growth of employees Fluency in English essential Possess board-certification including clinical experience in TAs/DAs of priority to the company and expertise in digital health is a plus Understanding of the local health care system, incl. regulatory and payer environment Who we are "

Role & responsibilities Patient Care: Diagnose and treat patients presenting with various medical conditions. Conduct medical assessments, including physical examinations and patient histories. Order and interpret diagnostic tests, such as blood tests and imaging studies. Prescribe medications and develop treatment plans. Monitor the progress of patients and make adjustments to treatment as necessary. Provide appropriate referrals to specialists when required Clinical Rounds: Participate in clinical rounds with the medical team to discuss patient cases, treatment plans, and outcomes. Communicate effectively with other healthcare professionals, including nurses, specialists, and support staff, to ensure coordinated patient care Medical Records: Maintain accurate and up-to-date patient records, including electronic health records (EHR). Document patient encounters, assessments, diagnoses, and treatment plans Emergency Response: Respond to medical emergencies within the hospital, including code blue and code red situations. Administer life-saving interventions and assist in resuscitation efforts. Continuous Learning: Stay current with medical research, guidelines, and best practices. Engage in continuing medical education and professional development activities. Compliance and Ethics: Adhere to hospital policies, medical ethics, and regulatory requirements. Maintain patient confidentiality and privacy. Qualifications: Medical degree (MBBS or equivalent). Appropriate medical licensure or registration to practice medicine. Completion of internship and residency programs, if required. Strong clinical and diagnostic skills. Effective communication and interpersonal skills. Ability to work well in a team and under pressure. Commitment to patient safety and quality care. Willingness to work in shifts, including nights and weekends, as required by the hospital.

Position - Lab Technician Qualification Required- DMLT/ BSc MLT Experience- 1- 5 years Role & responsibilities To perform assigned analytical testing procedures in an accurate, precise, and timely manner in the assigned lab. To perform routine and non-routine activities pertaining to laboratory testing and reporting and maintaining external and Internal Quality control Maintain required records and documentation. Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result. Analyze specimens using approved testing procedures as per SOP's, review and release test results. Adhere to the laboratory's quality control policies, instrument and procedural calibrations and follow safety guidelines as per established organization protocols.

We are looking for a medical officer who has completed MBBS with KMC registration for the Bangalore location with 6 hours working.

This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance s and defined regulatory strategies. He would even be responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. Your role at our organization is integral to helping the world meet new breakthroughs that affect generations to come, and we re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. Primary responsibilities include, but are not limited to: Regulatory Responsibilities: Provide input to global product and project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements and critically evaluating supporting documentation to assess acceptability and identify potential risks. Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements/variations, annual reports, registration renewals and responses to health authority questions per established business processes and systems. Liaise with global CMC, Our Manufacturing Division and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. Assess and communicate potential regulatory risks and propose mitigation strategies. Deliver all regulatory milestones for assigned products across the product lifecycle Identify and communicate potential regulatory issues to GRACS CMC management, as needed Technical Skills: Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills. Demonstrated understanding of related fields (eg, pharmaceutical manufacturing, analytical testing, and quality assurance). Proficient computer skills and previously demonstrated ability to operate in electronic document based GMP systems Leadership Skills: Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders. Demonstrated flexibility in responding to changing priorities or dealing with unexpected events. Capability to handle multiple priorities and balance work to achieve business goals. Demonstrated effective leadership, communication, and interpersonal skills Qualifications & Skills Bachelor s in Science, Engineering, or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry Minimum 5 - 7 yrs of Industry Pharmaceutical industry experience out of 4 years experience in managing CMC Regulatory submissions for small molecules/vaccines/biologics The candidate may be required to travel to other CMO sites on a need basis.

This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance s and defined regulatory strategies. He would even be responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. Primary responsibilities include, but are not limited to: Regulatory Responsibilities: Provide input to global product and project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements and critically evaluating supporting documentation to assess acceptability and identify potential risks. Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements/variations, annual reports, registration renewals and responses to health authority questions per established business processes and systems. Liaise with global CMC, Our Manufacturing Division and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. Assess and communicate potential regulatory risks and propose mitigation strategies. Deliver all regulatory milestones for assigned products across the product lifecycle Identify and communicate potential regulatory issues to GRACS CMC management, as needed Technical Skills: Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills. Demonstrated understanding of related fields (eg, pharmaceutical manufacturing, analytical testing, and quality assurance). Proficient computer skills and previously demonstrated ability to operate in electronic documentam based GMP systems Leadership Skills: Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders. Demonstrated flexibility in responding to changing priorities or dealing with unexpected events. Capability to handle multiple priorities and balance work to achieve business goals. Demonstrated effective leadership, communication, and interpersonal skills Qualifications & Skills Bachelor s in Science, Engineering, or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry Minimum 10 - 12 yrs of Industry Pharmaceutical industry experience out of 6 years experience in managing CMC Regulatory submissions for small molecules/vaccines/biologics. The candidate may be required to travel to other CMO sites on a need basis.

JD: 1) ECG Technician Support: Be available to provide real time support to ECG technicians if they have any technical or operation challenge 2) ECG Device Management: Keep track of the ECG devices and timely maintenance of them 3) ECG Training: Train field executive on how to effectively execute an ECG 4) Stakeholder Management: Coordinate with operation team, audit team and other key stakeholders to derive the best operational output Skills: 1) Candidate should know how to execute and interpret an ECG 2) Basic knowledge of google sheet/MS Excel Any past experience in PPMC/Insurance medical check up order execution will be an added advantage for the candidate Looking for immediate joiner Work from home also available Interested candidates share resume to whatsapp no. 8928285213 or mail to sanjay.behera@thyrocare.com

Job opening for Resident Medical Officer at Wockhardt Hospital Miraroad JOB DESCRIPTION OF RESIDENT MEDICAL OFFICER (RMO) Location- Mira Road Major Job Qualifications/Specific Skills Required Education: - MBBS Experience - Fresher or Experienced Technical competencies - Basic Life Support Behavioral Competencies - Good interpersonal skills - Good communication skills - People-oriented, flexible and adaptable - Decision making - Ability to handle pressure Job Summary - Prompt attention to patient - History Taking - Carry out pre-operative orders Key Responsibilities Principal Responsibilities - To attend any new patient (admission) immediately. - To take a proper history of the patient (If he is in a position to give it on his own) or from his relative. - Examine the patient. - Check any previous records, if available. - Charts down all the details in the history sheet. - Let the point or his relative go through all the details and take his signature on 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 theres a transfer in-patient from the ICU. Read the transfer summary carefully. See the point and examine him thoroughly. - Inform the respective consultants and carry out their orders. Inform the nursing staff if any changes. - To take rounds and examine individual patients. Inform the respective consultant/ Registrars if any new findings. - To follow up with all the investigations to be seen and trace their results. Inform the Registrar/ consultant. Note down investigation results in the investigation sheet. - To enter the treatment sheets for the following day. Cross check the same for the dosages of the medications. Confirm the investigations to be sending on the following day (As a cost of each and every investigation is very high). To take special precautions for any special investigations. - To enter pre-operative orders in the treatment sheet. To check whether the consent for the surgery has been taken from the patient. If not inform the respective person. To inform the Anesthetists on duty and instruct him / her about the patient. To carry out all the pre-operative orders. - To attend patients complaints. To calm the patients if they are apprehensive. Inform the consultant if needed. - To work with the hospital information system and other information technology resources and software as may be assigned on a periodic basis from time to time as per attached appendix Interested candidates can share their resume on nelson.dias@wockhardthospitals.com

Role Description The Compliance Surveillance function at Deutsche Bank is a global function which focuses on the post-event detection of market manipulation, insider trading and other risks as defined by established DB standards and regulatory requirements. The focal point of our activities is the monitoring of communication, voice, and trade data. The successful candidate will join the Compliance Surveillance function in Deutsche India Private Limited. The role involves working closely with colleagues to support the Germany region. Your key responsibilities Conduct daily surveillance - primarily on trade data - to detect potential breaches such as insider trading, market manipulative actions. Perform research and investigations within defined service levels to identify the reason for potential violations. Document research results and escalate violations and/or suspicious activity according to firm policy and regulatory requirements. Work with members of the broader Surveillance team (mostly the German Surveillance team) to identify, analyze, investigate, and resolve issues. Work on ad-hoc Surveillance tasks as needed. Your skills and experience Degree level preferably in finance or economics. Knowledge of Financial Markets and Financial Instruments and understanding of related risks (e.g., market abuse) as well as interest in financial news. At minimum two years of experience in Banking with exposure to Financial Instruments and / or Compliance. Fluent in spoken and written English. Being familiar with Mandarin or Cantonese is a plus. Strong attention to details, analytical skills and sound judgement. Team player with good communication skills with the ability to work independently. Proficiency in MS Office.

The Compliance Surveillance function at Deutsche Bank is a global function which focuses on the post-event detection of market manipulation, insider trading and other risks as defined by established DB standards and regulatory requirements. The focal point of our activities is the monitoring of communication, voice, and trade data. The successful candidate will join the Compliance Surveillance function in Deutsche India Private Limited. The role involves working closely with colleagues to support the Germany region. Your key responsibilities Conduct daily surveillance - primarily on trade data - to detect potential breaches such as insider trading, market manipulative actions. Perform research and investigations within defined service levels to identify the reason for potential violations. Document research results and escalate violations and/or suspicious activity according to firm policy and regulatory requirements. Work with members of the broader Surveillance team (mostly the German Surveillance team) to identify, analyze, investigate, and resolve issues. Work on ad-hoc Surveillance tasks as needed. Your skills and experience Degree level preferably in finance or economics. Knowledge of Financial Markets and Financial Instruments and understanding of related risks (e.g., market abuse) as well as interest in financial news. At minimum two years of experience in Banking with exposure to Financial Instruments and / or Compliance. Fluent in spoken and written English. Being familiar with Mandarin or Cantonese is a plus. Strong attention to details, analytical skills and sound judgement. Team player with good communication skills with the ability to work independently. Proficiency in MS Office.

Hiring for Register Pharmacist Fresh can also apply Location - Navi Mumbai (Juinagar) Salary - 17k to 24k in-hand Rotational shifts Rotational week off Required - Good Communication Qualification - B Pharma , M Pharma , D Pharma (With Registration). Interested person can share your Resume, will Surely get back to you .

This position typically refers to any employee within the EPD Medical organization with medical/scientific qualifications and training who provides scientific/medical support to EPD in a non-sales capacity, where the provision of such scientific/medical support includes significant contact with Abbott customers in the field. This definition is not intended to apply to those employees whose primary job function relates to the monitoring or management of clinical studies. Reporting into the Senior Manager RMA / Head RMA this position participates in the initiation, oversight and follow-up of assigned clinical studies and medical projects initiated within the EPD Medical Organization, ensuring that activities are carried out in accordance with relevant processes and procedures. The RMA interfaces with other key members of the EPD Medical Organization - for example, Medical Managers, Clinical Research Managers and Medical Advisors - relevant to the therapeutic area for which the RMA has responsibility. The RMA assists relationships and advances the scientific credibility of the Company with established and emerging Regional/National Opinion leaders, responds to requests for scientific and medical information, and provides key scientific information updates to Regional and National Opinion leaders, as appropriate. The RMA develops, and maintains, key scientific knowledge that will enable credible dissemination of scientific information and informed scientific dialogue with physicians and opinion leaders, and the development of professional working relationships. JOB RESPONSIBILITIES: Ensure that all activities and interactions are conducted with due regard to all applicable local, global and national laws, regulations, guidelines, codes of conduct, Company policies and accepted standards of best practice. Provide scientific and technical support for, and help maintain professional and credible relationships with, key opinion leaders and academic centers to ensure access to current medical and scientific information on the products and areas of therapeutic interest. Ideate, design, develop and deliver innovative and engaging high science activities for Physicians and Key Opinion Leaders, to help drive Therapy Shaping in the area the RMA is assigned to, in collaboration with the Medical Affairs the Commercial team. Assist in the initiation, oversight and follow up of assigned clinical studies and medical projects initiated within the relevant therapeutic area for which the RMA carries responsibility (e.g. post marketing clinical activities such as registry/database projects, epidemiological surveys, post-authorization studies (phase IV), IIS projects, etc.): all activities to comply with applicable local laws , guidelines, codes of practice, SOPs, and , ID SOPs. Deliver high science , unbiased and accurate scientific presentations to physicians, individually or in groups (meetings, clinical sessions, etc.), when requested. Participate in the selection process to identify appropriately qualified physicians the Company would wish to engage in collaborative efforts - such as potential research collaborations, or lecture/meeting support ( Round Tables , Congresses, Symposia, etc.); and to ensure a high level of scientific or educational integrity in these collaborative efforts. TECHNICAL COMPETENCIES: Therapeutic Area Expertise Management Skills Communication Skills Compliance Process Improvement Skills Problem/Conflict Solving Ability Priority Setting Relationship Building KEY INTERFACES: EPD medical personnel: Clinical Research Managers, Clinical Operations Managers, Medical Advisors; Medical Information team / specialists; EPD Pharmacovigilance / drug safety personnel Marketing department across therapeutic area Sales organization of the geographic area of responsibility. Administrative personnel of the Medical Department and of the Business Unit. Healthcare personnel (including; physicians, nurses, pharmacists). Patients (through Patient Awareness Programs) Participating Research Investigators Key Opinion leaders Institutions and Scientific or Medical Societies

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Responsible for conducting patient consultations, performing medical examinations, and interpreting diagnostic tests. Formulate accurate diagnoses, develop treatment plans, and prescribe medications as necessary. In addition to providing direct patient care, contribute to the development and implementation of hospital policies, participate in medical research, and engage in continuous professional development. Effective communication with patients, their families, and other healthcare professionals is vital for fostering a positive patient experience. MBBS, MD, and valid MMC Registration

Qualification - MBBS / BAMS Experience - 0-2 Years Job Duties & Responsibilities: To take daily rounds independently during assigned shifts and to countersign over all documentation done in progress sheet by Floor Managers. Routine rounds and coordination with consultants and documentation of their instructions / orders To evaluate and communicate with the consultants in case of critical clinical conditions/investigations for immediate actions. Filling the consent forms for ward procedures and counseling the Patient/relatives as and when required. Blood Requisition Form and Compatibility Reports to be filled/evaluated and countersigned properly. Transcribe and sign the daily medication orders in drug chart as per NABH guidelines. Patient Narcotics Sheet and Form 3E to be filled as per requirement. Perform minor procedures at the ward whenever required (e.g. wound dressing, suture/ catheter insertion/removal, etc.) Facilitate internal/external transfer of patients with necessary documentation. To facilitate TPA approvals in coordination with the TPA department. Preparation of discharge summary wherein Course in the Hospital, Condition at Discharge, Medication on Discharge and When to Obtain Urgent Care to be filled. All Discharge Summaries to be Signed by RMO before handing over to patient/relatives. Flexibility in doing Rotational Shifts as per the Hospitals needs. To be available for Camps arranged by the hospital. Q be present in the assigned floor/ wing during their shift. In case they have to leave the assigned floor for any reason during duty hours they should inform the Nursing Incharge and Medical Coordinator.Q