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Associate Medical Director, Patient Safety PhysicianJob Title: Associate Medical Director, Patient Safety PhysicianGlobal Career Level: EIntroduction to role:Are you ready to make bold moves in the field of oncology? As an Associate Medical Director, Patient Safety Physician, you will play a pivotal role in transforming the way cancer is treated. You will work independently or alongside senior safety physicians to evaluate adverse events and manage the safety profile of marketed products. Your expertise will be crucial in authoring regulatory documents and predicting the clinical implications of safety data. Join us in pushing the boundaries of science and making a meaningful difference in patients' lives!Accountabilities:As an Associate Medical Director, Patient Safety Physician, you will be responsible for signal detection, evaluation risk management activities, and labeling. You will provide medical input into the identification and utilization of information sources for signal evaluation, collaborate with external providers, and discuss data evaluation results with key stakeholders. Your strategic input will be vital in regulatory requests and safety evaluation documents. Additionally, you will contribute to regulatory reports and submissions, participate in external meetings, and maintain readiness for audits or inspections. Your collaboration across functions and cultures will drive innovation and process improvement.Essential Skills/Experience:<ul><li>Medical degree (eg MD, MBBS)</li><li>At least 2 years of clinical experience post-registration</li><li>High level of medical competence, with an ability to balance this with industry standards to achieve business goals</li><li>Minimum 3 years of Patient Safety experience (Pharmacovigilance) (with clear evidence of delivery)</li><li>Total of 6 to 11 years of experience</li></ul>Desirable Skills/Experience:<ul><li>Able to work across TAs and Functions</li><li>Experience of supervising Patient Safety colleagues</li><li>A demonstrated ability to understand epidemiological data</li></ul>Skills and Capabilities:<ul><li>Commitment to Customers and Integrity</li><li>Strategic Leadership</li><li>Acts Decisively</li><li>Drives Accountability</li><li>Works Collaboratively</li><li>Develops People and Organisation</li><li>May train or mentor junior level staff within given role</li></ul>Technical:<ul><li>Drug Development Experience and Application of Disease and TA knowledge</li><li>Integrative thinking</li><li>Excellence in pharmacovigilance</li><li>Patient Benefit risk assessment</li></ul>Core:<ul><li>Conceptual thinking</li><li>Influencing</li><li>Initiative</li><li>Innovation</li><li>Business relationship management</li></ul>When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.At AstraZeneca, you'll be part of a global team dedicated to eliminating cancer as a cause of death. With one of the broadest oncology pipelines in the industry, you'll have the opportunity to work on groundbreaking drug modalities and innovative approaches. Our collaborative environment fosters courage and curiosity, empowering you to take smart risks and challenge the norm. We are committed to making a meaningful impact on patients' lives through science-driven solutions.Ready to make a difference? Apply now and join us on our mission to transform cancer treatment!Date Posted27-Oct-2025Closing Date15-Nov-2025AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.<h4>Experience Level</h4>Mid Level

Astrazeneca India Private Limited

Clinical Nurse Specialist

Associate I Medical Writer<ul><li>Knowledge of safety guidelines and regulations for medical devices and/or pharmaceutical development and post-market surveillance</li><li>Familiarity with medical terminology and working with large databases.</li><li>Proven ability to analyze, interpret, and discuss safety information relating to multiple therapeutic areas.</li><li>Strong interpersonal, effective communication (written and verbal), and presentation skills.</li><li>Strong organization and time management skills</li><li>Demonstrates attention to detail and accuracy.</li><li>Self-motivated, ability to work under pressure, demonstrating initiative and flexibility.</li><li>High learning agility, ability to work independently and meet targeted timelines in a team-centric environment.</li><li>Experience with (safety or others) issue management</li></ul>ATTENTION: Current Alcon Employee/Contingent WorkerIf you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.<a href="https://wd5.myworkday.com/alcon/d/inst/1422$3/rel-task/3001$14.htmld" rel="noopener noreferrer" target="_blank">Find Jobs for Employees</a><a href="https://wd5.myworkday.com/alcon/d/inst/1422$130/rel-task/3001$14.htmld" rel="noopener noreferrer" target="_blank">Find Jobs for Contingent Worker</a>  Alcon is an Equal Opportunity Employer and takes pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital status, disability, or any other reason.<h4>Experience Level</h4>Mid Level

Alcon Laboratories India Pvt Ltd

Healthcare Transcriptionist

Dialysis Nurse- Position: Dialysis Nurse
- Location: Fortis Hospitals, Bannerghatta Road, Bangalore
- Responsibilities include providing care to patients undergoing dialysis treatment.
- The role may involve monitoring patient conditions, administering medications, and collaborating with healthcare teams.
- Candidates should have a strong understanding of dialysis procedures and patient management.
- The job may require working in a fast-paced environment and handling multiple patients.
- Further details on experience and qualifications are not specified.

Fortis Healthcare Limited

Dialysis Technician

Staff Nurse - NursingAssessment of patientsMonitoring of patientsEnsure safety of the patientAssist the Doctor in proceduresAdministering of medication following the 6 RightsCarry out investigation orders on timeMeeting the hygienic needs of the patient


 Dear Candidate,


 We are delighted to introduce you to Apollo Hospitals, a leading healthcare provider in India. With a long-standing heritage spanning many decades, Apollo Hospitals has established itself as a trusted name in the healthcare field, consistently delivering exceptional care with compassion.


 Renowned for our state-of-the-art medical facilities, advanced technology, and a highly skilled and dedicated team of healthcare professionals, Apollo Hospitals is committed to providing quality care and ensuring patient satisfaction in everything we do.


 Our organization strives to offer comprehensive healthcare services across various specialties and disciplines. From primary care to specialized treatments, we provide a wide range of medical services to cater to the diverse needs of our patients. Our hospital is equipped with cutting-edge technology, modern infrastructure, and an experienced team of doctors, nurses, and support staff who collaborate to deliver the highest standards of healthcare.


 At Apollo Hospitals, we believe in fostering continuous learning and innovation. We prioritize research and development to remain at the forefront of medical advancements, enabling us to provide the latest treatments and therapies to our patients. We also emphasize preventive care and wellness programs, promoting a healthy lifestyle and helping individuals maintain optimal health.


 Furthermore, Apollo Hospitals holds a strong commitment to social responsibility. Through various initiatives, we strive to make quality healthcare accessible to all members of society, regardless of their socio-economic background. We actively participate in community health programs, awareness campaigns, and outreach activities to promote healthcare education and support underserved populations.


 As you join our team, we invite you to embody the values and culture of Apollo Hospitals. Our core principles include prioritizing patient-centric care, fostering teamwork, upholding integrity, and embracing compassion in all that we do. Together, we have the power to make a significant impact on the lives of our patients and contribute to the progress of healthcare in our community.


 We are excited about the opportunity to collaborate with you, harnessing your skills and expertise to deliver exceptional care and service to our patients. If you have any inquiries or would like to explore more about Apollo Hospitals, please don't hesitate to contact our team.


 Thank you for joining the Apollo Hospitals family. We are thrilled to begin this journey together, striving for excellence in healthcare.


 Sincerely,


 Team HR<h4>Experience Level</h4>Senior Level

Apollo Hospitals Enterprise Limited

Staff Nurse

Literature Review Advisor<h4>Job Title: Literature Review Advisor</h4>Career Level - CIntroduction to role:Are you ready to make a difference in the pharmaceutical industry? As a Literature Review Advisor, you'll be at the forefront of ensuring the quality and accuracy of comprehensive literature reviews within the pharmaceutical sector. Working closely with the local PS team, you'll provide technical and operational support to the Literature Review Team, ensuring compliance with company and regulatory standards. Your role will involve building relationships with internal and external collaborators, supporting drug development, regulatory submissions, and clinical practice through insightful literature-based analysis. Dive into a dynamic environment where your analytical skills and understanding of pharmaceutical research methodologies will shine!<h4>Accountabilities:</h4><ul><li>Literature Review Procedures</li><li>Ensure the quality and comprehensiveness of literature searches, including the use of AstraZeneca databases.</li><li>Conduct reconciliations ensuring the accuracy of pharmacovigilance data that is transferred and received.</li><li>Oversee the identification, collection, and analysis of relevant scientific publications, clinical studies, and regulatory reports.</li><li>Keep up to date with industry developments, particularly automation and technology changes, to ensure AstraZeneca leads the way in conducting literature searches.</li><li>Collaboration &amp; Cross Functional Support</li><li>Collaborate with cross-functional teams (Marketing Company collaborators, R&amp;D, regulatory, medical affairs, clinical operations) to provide literature-based insights that inform drug development and regulatory strategies.</li><li>Work closely with subject matter experts to develop clear, concise, and scientifically sound literature materials, summaries, and reports.</li><li>Collaborate with external collaborators and/or academic institutions on literature review-related tasks.</li><li>Regulatory &amp; Compliance Adherence</li><li>Actively contribute to maintaining the core components of Good Pharmacovigilance Practice by contributing to all safety-related processes and brand activities within countries of remit and being audit and inspection ready.</li><li>Support external service providers to meet company and local regulatory PV requirements.</li><li>Complete all required patient safety trainings in adherence to internal processes and external regulations, obtaining access to relevant systems such as Safety Database, Regulatory systems, Human Resources systems, Quality Management Systems, and other global or local systems commercial databases as appropriate.</li><li>Maintain current and in-depth knowledge of:</li><li>Global and local procedural and guidance documents.</li><li>Marketed status of products in the local country and reference documents (i.e., Core Data Sheet).</li><li>Conditions, obligations, and other commitments relating to product safety or the safe use of AstraZeneca products.</li></ul><h4>Essential Skills/Experience:</h4><ul><li>Pharmacovigilance knowledge excellence</li><li>Good Pharmacovigilance Practice</li><li>Knowledge of health authority’s regulations</li><li>Cross functional collaborative approach</li><li>Effective and lateral thinking</li><li>Problem solving</li><li>Vendor management</li><li>Excellent attention to detail</li><li>Excellent written and verbal communication skills</li></ul><h4>Desirable Skills/Experience:</h4><ul><li>Influencing and Conflict Resolution skills</li><li>Medical knowledge in company Therapeutic Areas</li><li>Project management</li><li>Successful participation in above-market projects</li><li>Audit &amp; Inspection experience</li></ul>When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.AstraZeneca is where technology meets science to transform lives! Our work directly impacts patients by empowering the business to perform at its peak. With brand new digital technology platforms and data analytics, we drive exponential growth and redefine the industry. Here, you can innovate, take ownership, and explore new solutions in a environment. Join us on our journey to become a digital and data-led enterprise!Ready to make an impact? Apply now to join our team!Date Posted22-Oct-2025Closing Date23-Oct-2025AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.<h4>Experience Level</h4>Entry Level

Transcriptionist

Registrar - Radiology

 Dear Candidate,


 We are delighted to introduce you to Apollo Hospitals, a leading healthcare provider in India. With a long-standing heritage spanning many decades, Apollo Hospitals has established itself as a trusted name in the healthcare field, consistently delivering exceptional care with compassion.


 Renowned for our state-of-the-art medical facilities, advanced technology, and a highly skilled and dedicated team of healthcare professionals, Apollo Hospitals is committed to providing quality care and ensuring patient satisfaction in everything we do.


 Our organization strives to offer comprehensive healthcare services across various specialties and disciplines. From primary care to specialized treatments, we provide a wide range of medical services to cater to the diverse needs of our patients. Our hospital is equipped with cutting-edge technology, modern infrastructure, and an experienced team of doctors, nurses, and support staff who collaborate to deliver the highest standards of healthcare.


 At Apollo Hospitals, we believe in fostering continuous learning and innovation. We prioritize research and development to remain at the forefront of medical advancements, enabling us to provide the latest treatments and therapies to our patients. We also emphasize preventive care and wellness programs, promoting a healthy lifestyle and helping individuals maintain optimal health.


 Furthermore, Apollo Hospitals holds a strong commitment to social responsibility. Through various initiatives, we strive to make quality healthcare accessible to all members of society, regardless of their socio-economic background. We actively participate in community health programs, awareness campaigns, and outreach activities to promote healthcare education and support underserved populations.


 As you join our team, we invite you to embody the values and culture of Apollo Hospitals. Our core principles include prioritizing patient-centric care, fostering teamwork, upholding integrity, and embracing compassion in all that we do. Together, we have the power to make a significant impact on the lives of our patients and contribute to the progress of healthcare in our community.


 We are excited about the opportunity to collaborate with you, harnessing your skills and expertise to deliver exceptional care and service to our patients. If you have any inquiries or would like to explore more about Apollo Hospitals, please don't hesitate to contact our team.


 Thank you for joining the Apollo Hospitals family. We are thrilled to begin this journey together, striving for excellence in healthcare.


 Sincerely,


 Team HR

Medical Transcriptionist

Ward Secretary - OperationsJob Purpose                                      Qualification:Graduate; 1st division in 10th, 12th and Graduate, Diploma/Graduate/ Certificate CourseRelevant Experience:    <ul><li>1- 4 years of experience in Computer and typing knowledge.</li></ul>Responsibilities<ul><li>To receive the patient in the ward.</li><li>To inform the housekeeping and Executive in charge regarding new admission.</li><li>To keep a track of the approvals from the insurance company.</li><li>To obtain billing clearance before the patient goes for surgery.</li><li>To prepare a list of all the pending investigation reports and hand it over to the diagnostic counter.</li><li>To update the Activity chart of the patient on a daily basis.</li><li>To send the Activity chart to the billing department one day in advance of the proposed discharge of the patient.</li><li>To explain the discharge procedure to the patients.</li><li>To enter the track-sheets for the discharges and hand it over to the executive in charge on a daily basis.</li><li>To collect the feedback forms from the patients and forward it to Quality department.</li><li>To collect /dispatch blue folder from the medical records.</li></ul> Requirements and skills<ul><li>Familiarity with professional and technical emerging knowledge</li><li>Problem solving skills and ability to multi-task.</li><li>Compassionate with good communication skills.</li><li>Excellent teamwork skills</li><li>Graduate, Diploma/Graduate/ Certificate Course</li></ul>


 Dear Candidate,


 We are delighted to introduce you to Apollo Hospitals, a leading healthcare provider in India. With a long-standing heritage spanning many decades, Apollo Hospitals has established itself as a trusted name in the healthcare field, consistently delivering exceptional care with compassion.


 Renowned for our state-of-the-art medical facilities, advanced technology, and a highly skilled and dedicated team of healthcare professionals, Apollo Hospitals is committed to providing quality care and ensuring patient satisfaction in everything we do.


 Our organization strives to offer comprehensive healthcare services across various specialties and disciplines. From primary care to specialized treatments, we provide a wide range of medical services to cater to the diverse needs of our patients. Our hospital is equipped with cutting-edge technology, modern infrastructure, and an experienced team of doctors, nurses, and support staff who collaborate to deliver the highest standards of healthcare.


 At Apollo Hospitals, we believe in fostering continuous learning and innovation. We prioritize research and development to remain at the forefront of medical advancements, enabling us to provide the latest treatments and therapies to our patients. We also emphasize preventive care and wellness programs, promoting a healthy lifestyle and helping individuals maintain optimal health.


 Furthermore, Apollo Hospitals holds a strong commitment to social responsibility. Through various initiatives, we strive to make quality healthcare accessible to all members of society, regardless of their socio-economic background. We actively participate in community health programs, awareness campaigns, and outreach activities to promote healthcare education and support underserved populations.


 As you join our team, we invite you to embody the values and culture of Apollo Hospitals. Our core principles include prioritizing patient-centric care, fostering teamwork, upholding integrity, and embracing compassion in all that we do. Together, we have the power to make a significant impact on the lives of our patients and contribute to the progress of healthcare in our community.


 We are excited about the opportunity to collaborate with you, harnessing your skills and expertise to deliver exceptional care and service to our patients. If you have any inquiries or would like to explore more about Apollo Hospitals, please don't hesitate to contact our team.


 Thank you for joining the Apollo Hospitals family. We are thrilled to begin this journey together, striving for excellence in healthcare.


 Sincerely,


 Team HR<h4>Experience Level</h4>Mid Level

Ward Secretary

Technician - Laboratory Services

 Dear Candidate,


 We are delighted to introduce you to Apollo Hospitals, a leading healthcare provider in India. With a long-standing heritage spanning many decades, Apollo Hospitals has established itself as a trusted name in the healthcare field, consistently delivering exceptional care with compassion.


 Renowned for our state-of-the-art medical facilities, advanced technology, and a highly skilled and dedicated team of healthcare professionals, Apollo Hospitals is committed to providing quality care and ensuring patient satisfaction in everything we do.


 Our organization strives to offer comprehensive healthcare services across various specialties and disciplines. From primary care to specialized treatments, we provide a wide range of medical services to cater to the diverse needs of our patients. Our hospital is equipped with cutting-edge technology, modern infrastructure, and an experienced team of doctors, nurses, and support staff who collaborate to deliver the highest standards of healthcare.


 At Apollo Hospitals, we believe in fostering continuous learning and innovation. We prioritize research and development to remain at the forefront of medical advancements, enabling us to provide the latest treatments and therapies to our patients. We also emphasize preventive care and wellness programs, promoting a healthy lifestyle and helping individuals maintain optimal health.


 Furthermore, Apollo Hospitals holds a strong commitment to social responsibility. Through various initiatives, we strive to make quality healthcare accessible to all members of society, regardless of their socio-economic background. We actively participate in community health programs, awareness campaigns, and outreach activities to promote healthcare education and support underserved populations.


 As you join our team, we invite you to embody the values and culture of Apollo Hospitals. Our core principles include prioritizing patient-centric care, fostering teamwork, upholding integrity, and embracing compassion in all that we do. Together, we have the power to make a significant impact on the lives of our patients and contribute to the progress of healthcare in our community.


 We are excited about the opportunity to collaborate with you, harnessing your skills and expertise to deliver exceptional care and service to our patients. If you have any inquiries or would like to explore more about Apollo Hospitals, please don't hesitate to contact our team.


 Thank you for joining the Apollo Hospitals family. We are thrilled to begin this journey together, striving for excellence in healthcare.


 Sincerely,


 Team HR

Laboratory Technician

Territory Manager<h4>Company Description</h4>Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable.  Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparencyDr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.<h4>Additional Information</h4>About the Department Global Generics India Global Generics India business journey began in 1986. In the last three decades, we have grown as a trusted name in the healthcare industry and rank as one of the top 10 Pharma Companies in the Indian Pharma Market (IPM) as per IQVIA MAT (November 2022). Our commitment to Lead Ahead has helped us move ranks from 16th position to 10th position (IPM) in the last four years. We are a fast-growing organisation with double-digit growth and significant market share in domestic markets. Currently, we rank among the top 5 in oncology, anti-allergy and gastrointestinal diseases and the top 10 in a few other therapy areas. Our focus is on leveraging our digital capabilities, collaborations, innovations and inorganic opportunities to become the top 5 companies in the Indian Pharma Market. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/ <h4>Experience Level</h4>Mid Level

Dr Reddys Laboratories

Territory Manager

Regional Medical Advisor<h4>Company Description</h4>Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable.  Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparencyDr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.<h4>Job Description</h4>Job Summary We are looking for the Primary scientific face of the organization to ‘Thought Leaders’ &amp; physicians for a given therapy area. You will be responsible for Identification, mapping and profiling of thought leaders of given geography and therapy area, on an ongoing basis. Roles &amp; 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 &amp; 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. <h4>Qualifications</h4>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. Skills &amp; attributes –  Technical Skills  • 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. Behavioural Skills • Integrity driven decision making skills  • Collaboration and teaming with ability to work in a matrix environment  • Strategic thinking &amp; sound analytical skills  • Big picture orientation with attention to detail  • Sense of urgency &amp; desire to excel  • Intellectual curiosity  • Self-awareness and adaptability  • Result oriented and performance driven  • Excellent interpersonal &amp; communication skills to effectively interact with a broad range of audience.<h4>Additional Information</h4>About the Department Global Generics India Global Generics India business journey began in 1986. In the last three decades, we have grown as a trusted name in the healthcare industry and rank as one of the top 10 Pharma Companies in the Indian Pharma Market (IPM) as per IQVIA MAT (November 2022). Our commitment to Lead Ahead has helped us move ranks from 16th position to 10th position (IPM) in the last four years. We are a fast-growing organisation with double-digit growth and significant market share in domestic markets. Currently, we rank among the top 5 in oncology, anti-allergy and gastrointestinal diseases and the top 10 in a few other therapy areas. Our focus is on leveraging our digital capabilities, collaborations, innovations and inorganic opportunities to become the top 5 companies in the Indian Pharma Market. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/ <h4>Experience Level</h4>Mid Level

Medical Representative

Premium Billing Analyst•	Primary skills:Domain-&gt;Healthcare-&gt;Healthcare - ALL,Technology-&gt;Oracle Industry Solutions-&gt;Oracle Revenue Management &amp; Billing(ORMB) •	Ability to work with clients to identify business challenges and contribute to client deliverables by refining, analyzing, and structuring relevant data
•	Awareness of latest technologies and trends
•	Logical thinking and problem solving skills along with an ability to collaborate
•	Ability to assess the current processes, identify improvement areas and suggest the technology solutions 
•	One or two industry domain knowledge A day in the life of an Infoscion
•	As part of the Infosys consulting team, your primary role would be to actively aid the consulting team in different phases of the project including problem definition, effort estimation, diagnosis, solution generation and design and deployment 

•	You will explore the alternatives to the recommended solutions based on research that includes literature surveys, information available in public domains, vendor evaluation information, etc. and build POCs 

•	You will create requirement specifications from the business needs, define the to-be-processes and detailed functional designs based on requirements.

•	You will support configuring solution requirements on the products; understand if any issues, diagnose the root-cause of such issues, seek clarifications, and then identify and shortlist solution alternatives

•	You will also contribute to unit-level and organizational initiatives with an objective of providing high quality value adding solutions to customers. 

If you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you!

Infosys

Billing Specialist

Senior Process Analyst - RCMHuron helps its clients drive growth, enhance performance and sustain leadership in the markets they serve. We help healthcare organizations build innovation capabilities and accelerate key growth initiatives, enabling organizations to own the future, instead of being disrupted by it. Together, we empower clients to create sustainable growth, optimize internal processes and deliver better consumer outcomes. Health systems, hospitals and medical clinics are under immense pressure to improve clinical outcomes and reduce the cost of providing patient care. Investing in new partnerships, clinical services and technology is not enough to create meaningful and substantive change. To succeed long-term, healthcare organizations must empower leaders, clinicians, employees, affiliates and communities to build cultures that foster innovation to achieve the best outcomes for patients. Joining the Huron team means you’ll help our clients evolve and adapt to the rapidly changing healthcare environment and optimize existing business operations, improve clinical outcomes, create a more consumer-centric healthcare experience, and drive physician, patient and employee engagement across the enterprise. Join our team as the expert you are now and create your future.As a Senior Process Analyst, you will be involved in the full lifecycle of RCM. Responsibilities include working in RCM functions like EOB review, Payment Posting, Correspondence review, Bad Debt, Appeals process, Denial management and Account receivables. Strong analytical skills and typing speed is a must. Daily productivity targets to be met. Excellent communication skills, attention to detail, and strong technical and problem solving skills are essential aspects of this role.JOB DETAILS: • Good comm skills with neutral accent • Good English Written and Listening skills • Willing to work in US shift timings • Net typing speed of 30 words per min &amp; above with an accuracy rate of 90% + • Good knowledge about MS Office tools • Solve complex scope wise problems with little or no supervision from lead • Interact with key stakeholders • Develop in-depth knowledge of business processes facilitated by our software products • Develop in-depth knowledge of operational processes around the scope of work. • Troubleshoot deployment and environmental issues, resolve issues in a timely manner across multiple projects. QUALIFICATIONS: • 2+ years of industry experience • 2+ year Experience in AR Calling with EPIC is a must. Proficiency in Excel and typing is a must. Familiarity with Cerner applications and other related applications • Ability to adapt quickly to new and changing technical environments as well as strong analytical, problem solving and quantitative abilities. Solid verbal and written communication skills are required. Graduate in Commerce, computer applications . Education/Certifications: • Graduate<h4>Position Level</h4>Senior Analyst<h4>Country</h4>India<h4>Experience Level</h4>Senior Level

Huron Eurasia India Private Limited

Process Analyst

Executive, Formulation Dev-ARPL-FD AR
About Apotex Inc.Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.For more information visit: <a href="http://www.apotex.com/">www.apotex.com</a>. <h4>Job Summary</h4><ul><li>This role will develop experimental approaches and will be responsible for analyzing scientific results from experiments. Generating accurate, reliable data by following established procedures and practices to support product development.</li><li>Responsible for formula optimization experiments and process optimization trials by employing the concept of Identification of Quality Target Product Profile (QTPP), Critical Material Attributes (CMAs), Critical Process Parameters (CPPs) and its effect on drug product Critical Quality Attributes (CQAs) during the initial drug product development stage.</li><li>Responsible for assisting in execution of early development, scale-up, stability, submission, placebo batches to develop new and modified product formulations, and for packaging – filling and/or sealing – quality pharmaceutical products in a variety of finished goods formats. The Technician works and ensures that all operations are performed in accordance with applicable procedures.  The person is an expert at basic skills in Formulation Development.</li></ul><h4>Job Responsibilities</h4><ol><li>Executes process evaluation, experimental, optimization, Bio / Submission batches and scale-up trials and batches as per instructions.</li><li>Weighs, mixes, screens and blends raw materials to produce experimental trials, pilot and small-scale batches for compressed, enteric coated, and film coated tablets, capsules, pellets, powders, liquids and others as required.</li><li>Dismantles, cleans, sanitizes and assembles, as required, formulation development rooms and equipment according to established SOPs and Technical Manuals to ensure GMP compliance and meet schedule requirements.</li><li>Performs in-process quality tests on trials and production batches for weight, hardness, thickness, friability, disintegration, etc. as required.</li><li>Delivers in-process samples to the designated area. Maintains in-process testing lab.</li><li>Completes and signs off all process documentation required during the execution of a batch.</li><li>Recognizes out of normal situations and uses conventional problem-solving skills to identify the root cause and troubleshoot problems, provides feedback to the supervisor, and seeks assistance as required.</li><li>Recommends modifications to methodology used in trials and optimization where there are opportunities to improve processes / procedures.</li><li>Reviews trial and batch documentation for correctness and completeness before forwarding to Supervisor.</li><li>Deducts raw materials from inventory where required.</li><li>Participates in operating the current Packaging equipment within specifications.</li><li>Conducts basic troubleshooting of the entire Packaging operations.</li><li>Works as a member of a team to achieve all outcome</li><li>Works in a safe manner collaborating as a team member to achieve all outcomes.</li><li>Responsible for development and design of formulations for multiple products selected for development &amp; conducting meeting with multidisciplinary teams.</li><li>Conducts relevant patent searches on formulations. Reviews scientific literature and makes recommendations for formulation development strategies.</li><li>Attends appropriate trainings, seminars, and presentations to maintain expertise in formulations and related areas.</li><li>Communicates with buyers and peers to ensure that APIs, excipients, tooling etc. are available for the project in required quantities, as and when needed.</li><li>Liaises with the plant operation supervisors and scheduler to ensure that experimental trials / registration batches are planned and executed in a timely manner.</li><li>Liaises with the documentation groups to ensure that early development trial documents, process evaluation and process optimization documents required for execution.</li><li>Coordinates with lab for sample requirement and provides timelines for testing of samples.</li><li>Coordinates with documentation for timely project manufacturing and packaging documents.</li><li>Coordinates with documentation for timely regulatory submission of scale-up documents.</li><li>Possesses a detailed understanding of the theoretical principles for major manufacturing and a working knowledge of the equipment used in the manufacturing processes and ensures successful execution of experimental trials / registration batches on floor.</li><li>Investigates formulation/process issues, finds root causes, plans corrective action.</li><li>Works as a member of a team to achieve all outcomes.</li><li>Works in a safe manner collaborating as a team member to achieve all outcomes.</li><li>Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance and Passion.</li><li>Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.</li><li>All other relevant duties as assigned.</li></ol><h4>Job Requirements</h4><ul><li>Education
<ul><li>Diploma or in Chemistry, Pharmaceutical Technology, Engineering, or related science would be an asset. </li></ul></li><li>Knowledge, Skills and Abilities
<ul><li>Excellent working and theoretical knowledge of different pharmaceutical solid oral dosage forms such as immediate release, controlled release &amp; delayed release dosage forms</li><li>Detailed understanding of the theoretical principles for major manufacturing processes and equipment.</li><li>Strong verbal and written English communication skills.</li><li>Experience using computers, preferable in MS Office (Word, Excel, PowerPoint, Outlook).</li><li>Well-developed interpersonal and team skills.</li><li>Knowledge of GMP, GLP, GDP, Safety, FDA and TPD guidelines.</li><li>Multi-tasking and project management skills.</li></ul></li></ul><ul><li>Experience
<ul><li>4-6 years of working experience in a pharmaceutical development environment with related experience in formulation development of solid oral dosage forms for regulated market, scale up and/or technology transfer.</li></ul></li></ul>At Apotex, we are committed to fostering a welcoming and accessible work environment, where all everyone feels valued, respected, and supported to succeed. We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation. <h4>Experience Level</h4>Executive Level

Apotex Pharmachem India Pvt Ltd

Product Executive

Medical Transcriptionist- Job Title: Medical Transcriptionist
- Location: Bangalore
- The role involves transcribing medical reports and documents.
- Candidates should be proficient in medical terminology.
- Attention to detail is crucial for accuracy in transcription.
- Familiarity with transcription software may be beneficial.
- The job may require working with healthcare professionals to ensure clarity in documentation.
- No specific experience requirements are mentioned, making it suitable for various candidates.
- The job is located in IHL-Rajajinagar, Bangalore.

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