326 Endocrinology Jobs - Page 2

KAILASH HOSPITAL, GREATER NOIDA is looking for Senior Resident- Pediatric to join our dynamic team and embark on a rewarding career journey Patient Care: Provide comprehensive medical care to patients under the supervision of attending physicians Perform physical examinations, diagnose medical conditions, develop treatment plans, and monitor patient progress Clinical Supervision: Supervise and provide guidance to junior residents, interns, and medical students in their clinical duties Assist in their training, evaluation, and professional development Hospital Rounds: Conduct regular hospital rounds to assess patients, review test results, and discuss treatment plans with the healthcare team Coordinate and communicate patient care plans with nurses, specialists, and other healthcare professionals Medical Procedures: Perform or assist in various medical procedures, such as venipuncture, wound care, suturing, and bedside procedures Ensure adherence to sterile techniques, safety protocols, and best practices Medical Documentation: Maintain accurate and up-to-date medical records, including patient history, physical examination findings, treatment plans, and progress notes Ensure compliance with legal and regulatory requirements Patient Education: Educate patients and their families about their medical conditions, treatment options, and preventive measures Provide counseling on lifestyle modifications, medication management, and post-discharge care instructions Interdisciplinary Collaboration: Collaborate with other healthcare professionals, including nurses, pharmacists, therapists, and social workers, to ensure coordinated and holistic patient care Participate in interdisciplinary team meetings and contribute to care planning Continuity of Care: Facilitate smooth transitions of care between inpatient and outpatient settings Coordinate follow-up appointments, referrals, and discharge planning to ensure continuity of care and optimal patient outcomes Medical Research and Education: Stay updated with the latest medical advancements, evidence-based practices, and clinical guidelines Engage in research activities, present at conferences, and contribute to medical education and scholarly activities Quality Improvement: Participate in quality improvement initiatives to enhance patient safety, clinical outcomes, and healthcare delivery Identify areas for improvement, implement evidence-based practices, and contribute to quality assurance programs Professional Development: Engage in continuing medical education (CME) activities, attend conferences, and pursue opportunities for professional growth Maintain licensure and board certification requirements

Neurosurgeon Required at Bhiwani Haryana Salary 6 to 7 Lakhs + Accommodation Azamgarh UP Team Work Salary 5 to 6 Lakhs + Accommodation Sirsa Haryana Salary 6 to 7 Lakhs + Accommodation Required Candidate profile Gurdaspur Punjab Salary 6 to 7 Lakhs + Accommodation Batala Punjab Salary 6 to 7 Lakhs + Accommodation Doctor couple can be adjusted in their respective branch

General & Laparoscopic Surgeon Required at Gohana Haryana Salary 3.5 to 4 Lakhs + Accommodation Bhiwani Haryana Male Required Salary 3.5 Lakhs + Accommodation Ambedkar Nagar UP Salary 3.5 Lakhs + Veraval Gujarat Salary 3 Lakhs + Accommo Required Candidate profile Gadchiroli Maharashtra Peripheral Location Salary 3.5 Lakhs + Accommodation + Food Charkhi Dadri Haryana Male Required Salary 3.5 Lakhs + Accommodation

MD Medicine required at Bhiwani Haryana Salary 3.5 to 4 Lakhs + Accommodation Rohtak Haryana Salary 3.5 Lakhs + Accommodation Rewari Haryana Salary 3.5 to 4 Lakhs + Accommodation Jagdishpur UP Salary 3.5 to 4 Lakhs + Accommodation Required Candidate profile Azamgarh UP Salary 3.5 Lakhs + Share + Accommodation Ambedkar Nagar UP Salary 3.5 Lakhs + Jhajjar Haryana Salary 3.5 to 4 Lakhs + Accommodation Varanasi UP Salary 2.5 to 3 Lakhs

Cardiologist Required at Chandigarh Salary 5 Lakhs + Share Goalpara Assam Salary 10 Lakhs + Share + Accommodation Rohtak Haryana Salary 8 Lakhs + Accommodation Lucknow UP Salary 6 to 7 Lakhs Tohana Haryana Salary 8 Lakhs + Share + Required Candidate profile Bathinda Punjab Salary 6 Lakhs + Share + Accommodation Gurdaspur Punjab Salary 7 to 8 Lakhs for 5 Years + Experience Hoshiarpur Punjab Salary 8 Lakhs + Accommodation + Share

Psychiatrist Required Azamgarh UP Salary 2.5 Lakhs + Accommodation *Benefits:* - Doctor couples can be placed at the same location. - Assistance in finding suitable jobs based on preferred locations.

Mumbai, India (hybrid role: 3 days office, 2 days home per week) Salary: Competitive + Benefits + Bonus If you are an agile, committed, and detail-oriented pharmacovigilance professional with 8+ years of total PV experience, including a minimum of 4-5 years in authoring aggregate safety reports and Risk Management Plans (RMPs) and have additional experience overseeing ICSR compliance activities at both local and global levels, then we would love to hear from you. Join us to help improve peoples lives and make healthcare better for everyone! Why Pharmanovia? Pharmanovia is a dynamic, fast-growing international pharmaceutical company with a portfolio of over 20 brands across more than 160 markets. Our mission is to improve patient health globally through the revitalisation of niche, tried-and-trusted medicines. Our core behaviours are: We act decisively but we never compromise on quality. We keep our promises and do as we say. We value our heritage and foster an entrepreneurial spirit. We reinvest in our future - in our products, our brands and our people. We give back to our communities. Since its inception in 2013, Pharmanovia has grown consistently year on year, focusing on delivering high-quality branded prescription medicines to patients, prescribers, and healthcare providers across the world. Our growth has enabled the company to reinvest in its products, brands, people, and to give back to its communities. A people business with a strong, supportive culture that encourages innovation and entrepreneurial spirit, our team comprises over 300 employees and 29 nationalities, operating from offices in the UK, Denmark, Netherlands, Switzerland, Italy, Spain, Germany, U.A.E., India, China, Australia and Singapore. We are an agile, committed, and innovative global specialty pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the life cycle management of iconic medicines. We seek to extensively engage with clinical communities to communicate product improvements and prioritise environmental, social, and governance considerations across the business and workforce. Pharmanovias therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology. Main responsibilities & duties: Prepare and author aggregate safety reports and regulatory documents, including PADERs, Summary Evaluation Reports (SERs), and Serious Adverse Reaction (SAR) reports Prepare and author Risk Management Plans (RMPs) Provide strategic oversight and operational management of SDEAs, including authoring, reviewing, and ensuring ongoing compliance Ensure compliance with ICSR submission timelines and partner obligations Develop and maintain internal processes to support core pharmacovigilance activities Support and participate in pharmacovigilance audits and regulatory inspections Contribute to product labelling activities based on safety data and evolving benefit-risk profiles Monitor and assess regulatory intelligence updates and implement necessary changes to PV systems and practices Assist with pharmacovigilance risk assessments and due diligence activities for new products or partnerships Develop, track, and report key performance indicators (KPIs) to senior leadership for informed decision-making Collaborate cross-functionally with internal leadership teams to ensure PV oversight aligns with broader business goals About you: Candidates with progressive pharmacovigilance experience, specifically in authoring aggregrate reports, RMPs, as well as management and oversight of SDEAs and ICSR compliance activities, should have the skills and experience required for the role. We are also looking for: Bachelors degree in Pharmacy (Masters degree desirable) 8+ years of experience in pharmacovigilance with minimum 4-5 years of experience in authoring aggregate reports/RMPs is essential. Experience in working with core pharmaceutical companies desirable Strong knowledge of PV regulations at local and global level Experience in management of SDEAs Experience in ICSR review and compliance monitoring Organised and inquisitive, with problem solving skills Solid time management skills, the ability to multitask and see the big picture Strong technical skills Adaptability and resilience What we offer: We offer a competitive salary plus bonus and rewards package including holiday, health & wellbeing program, employee recognition awards, social events, pension scheme and hybrid working. By applying for this role, your details will be sent to Ortolan People, who are engaged to provide recruitment support in processing applications. We will endeavour to respond to all applicants within three working days. Occasionally for roles with a very high volume of applicants, this may not be possible. Enter Your Details Please fill out all form fields and upload your CV If you would like to know more about Ortolan People and how we can help you reduce your ongoing recruitment costs, get in touch! Hope started operating in 2013 and we had a lot of positions that we needed to fill. We initially relied on recruitment agencies and did a little bit of our own direct advertising, but wanted to explore more cost effective recruitment methods. We decided to try some e-recruiters to see how they could help. Ortolan were by far the best and also the most cost effective of the suppliers that we tried and we now ask for their help with virtually all of our external recruitment needs, because they provide a very personal and tailored service, have people, rather than computers, working on their candidate searches and short lists. Using Ortolan has significantly reduced our expenditure on attracting candidates, but has also meant that we have had a much broader range of people applying to work for us than before. I d highly recommend trying Ortolan to see how they can help you. Peter Spargo, HR Manager, Hope Construction Materials Ltd Nick Benson Chief Executive I am a solicitor who as well as having had a 10 year career as a British Army officer has also run a number of successful businesses. I have worked in large law firms, small start-up businesses and have been the CEO of a NASDAQ listed international leisure company. Drawing on this broad base of experience I co-founded Ortolan Group in 2007, driven by the opportunity to provide innovative and high quality recruitment services at a sensible price point. Today I help to manage the business and also spend a lot of time working as a solicitor with our sister company, Ortolan Legal. Because of my background, I tend to lead on all of our legal recruitment work. I occupy my spare time raising Tamworth pigs and flying. Cindy Parry Senior Consultant Having spent most of my working life in Recruitment and HR, I sold my successful Recruitment Business in 2009 to a large national High Street agency. Having missed the recruitment industry too much to stay away! I joined Ortolan in 2013 and I now head up their Permanent Recruitment Division. I live in Cheshire with my husband and unruly pack of 4 very large dogs, and as I don t work Mondays love to spend long weekends out and about in the countryside with the dogs, and ever so occasionally shopping for handbags and shoes! Jane Johnstone Senior Consultant After attaining an engineering degree and working for British Gas designing distribution systems, I had a change of career and joined British Aerospace as a computer programmer. I then spent twenty years working for major IT solutions vendors in a range of roles (product and sales support, professional services, technical management), before I had my next change of career into recruitment in 2008, when I moved from South East to Derbyshire. In my spare time I like to explore the Peak District, then reward myself with a pub lunch!

Medpace is currently looking for Clinical Trial Manager (CTM) to lead global clinical research studies. This position is fully office-based in our Mumbai, India office. Medpace is a scientifically led organization involved in full services for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials. Responsibilities The Clinical Trial Manager position performs project lead role for multiservice global clinical trials. The position interacts with sponsors and manages the timeline and project deliverables. This role coordinates for all services contracted for the study. CTMs are also responsible for leading cross functional team of clinical monitoring, study start-up, regulatory, contract, safety, medical monitoring etc. CTM may need to attend bid defense meetings and support business development team in winning new business. Qualifications Bachelor’s degree in a health related field (Master’s degree or PhD is preferred); At least two years of clinical trial management experience in Asia Pacific region ideally in a CRO environment; Experience in Cardiovascular, Renal & Metabolic Disease (CVRM) studies required; Excellent communication skills including good written and spoken English; and Flexible, accountable and comfortable in working in a global environment. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Associate Manager, Pharmacovigilance Mumbai, India (hybrid role: 3 days office, 2 days home per week) Salary: Competitive + Benefits + Bonus If you are an agile, committed, and detail-oriented pharmacovigilance professional with 8+ years of total PV experience, including a minimum of 4-5 years in authoring aggregate safety reports and Risk Management Plans (RMPs) and have additional experience overseeing ICSR compliance activities at both local and global levels, then we would love to hear from you. Join us to help improve peoples' lives and make healthcare better for everyone! Why Pharmanovia? Pharmanovia is a dynamic, fast-growing international pharmaceutical company with a portfolio of over 20 brands across more than 160 markets. Our mission is to improve patient health globally through the revitalisation of niche, tried-and-trusted medicines. Our core behaviours are: We act decisively but we never compromise on quality. We keep our promises and do as we say. We value our heritage and foster an entrepreneurial spirit. We reinvest in our future - in our products, our brands and our people. We give back to our communities. Since its inception in 2013, Pharmanovia has grown consistently year on year, focusing on delivering high-quality branded prescription medicines to patients, prescribers, and healthcare providers across the world. Our growth has enabled the company to reinvest in its products, brands, people, and to give back to its communities. A people business with a strong, supportive culture that encourages innovation and entrepreneurial spirit, our team comprises over 300 employees and 29 nationalities, operating from offices in the UK, Denmark, Netherlands, Switzerland, Italy, Spain, Germany, U.A.E., India, China, Australia and Singapore. We are an agile, committed, and innovative global specialty pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the life cycle management of iconic medicines. We seek to extensively engage with clinical communities to communicate product improvements and prioritise environmental, social, and governance considerations across the business and workforce. Pharmanovia's therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology. Main responsibilities & duties: Prepare and author aggregate safety reports and regulatory documents, including PADERs, Summary Evaluation Reports (SERs), and Serious Adverse Reaction (SAR) reports Prepare and author Risk Management Plans (RMPs) Provide strategic oversight and operational management of SDEAs, including authoring, reviewing, and ensuring ongoing compliance Ensure compliance with ICSR submission timelines and partner obligations Develop and maintain internal processes to support core pharmacovigilance activities Support and participate in pharmacovigilance audits and regulatory inspections Contribute to product labelling activities based on safety data and evolving benefit-risk profiles Monitor and assess regulatory intelligence updates and implement necessary changes to PV systems and practices Assist with pharmacovigilance risk assessments and due diligence activities for new products or partnerships Develop, track, and report key performance indicators (KPIs) to senior leadership for informed decision-making Collaborate cross-functionally with internal leadership teams to ensure PV oversight aligns with broader business goals About you: Candidates with progressive pharmacovigilance experience, specifically in authoring aggregate reports, RMPs, as well as management and oversight of SDEAs and ICSR compliance activities, should have the skills and experience required for the role. We are also looking for: Bachelor's degree in Pharmacy (Master's degree desirable) 8+ years of experience in pharmacovigilance with minimum 4-5 years of experience in authoring aggregate reports/RMPs is essential. Experience in working with core pharmaceutical companies desirable Strong knowledge of PV regulations at local and global level Experience in management of SDEAs Experience in ICSR review and compliance monitoring Organised and inquisitive, with problem solving skills Solid time management skills, the ability to multitask and see the big picture Strong technical skills Adaptability and resilience What we offer: We offer a competitive salary plus bonus and rewards package including holiday, health & wellbeing program, employee recognition awards, social events, pension scheme and hybrid working. By applying for this role, your details will be sent to Ortolan People, who are engaged to provide recruitment support in processing applications. We will endeavour to respond to all applicants within three working days. Occasionally for roles with a very high volume of applicants, this may not be possible.

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Research (CRA) Manager to join our Clinical Monitoring team in Navi Mumbai, India. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities Line management of Clinical Research Associates (CRAs); Recruitment, initial and continued training and development of CRAs; Oversight and Management of CRAs to ensure CRAs are meeting expectations of core monitoring responsibilities; Tracking and management of CRA resourcing/allocation of assignment; and Manage turnover and retention of CRAs to meet company objectives Qualifications Bachelor’s degree with 4-6 years pharmaceutical industry experience (clinical monitoring or study management), including 3 years as a CRA, and 1-2 years as a CRA Manager preferred; Advanced knowledge of Good Clinical Practice; Strong leadership, mentoring, and motivational skills; Effective written and verbal communication skills; Proficient knowledge of Microsoft® Office software; and Occasional travel for evaluation of CRAs (approximately 10%); Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

As a Senior Specialist in Endocrinology, you will be responsible for diagnosing, treating, and managing disorders of the endocrine system. This includes hormonal imbalances, metabolic diseases, and chronic endocrine conditions. The role involves direct patient care, interdisciplinary collaboration, education, and participation in clinical research. Key Responsibilities: Patient Evaluation and Diagnosis: Conduct comprehensive medical histories and physical examinations. Order and interpret diagnostic tests such as hormone levels, imaging studies, and biopsies. Diagnose endocrine conditions accurately through analysis of symptoms and medical data. Monitor patients growth, development, and overall health related to endocrine disorders. Treatment Planning and Management: Develop individualized treatment plans based on patient diagnosis, condition severity, and preferences. Prescribe and adjust medications to manage hormonal imbalances and related diseases. Educate patients on their conditions, treatment options, and necessary lifestyle modifications. Collaborate with allied health professionals (e.g., dieticians, psychologists) to provide holistic care. Chronic Disease Management: Monitor patients with chronic endocrine disorders such as diabetes, thyroid disease, and adrenal dysfunction. Design long-term strategies to improve health outcomes and prevent complications. Modify treatment plans based on patient progress and clinical findings. Train patients in self-management techniques like insulin use and hormone therapy. Research and Education: Stay abreast of the latest developments in endocrinology through ongoing education and literature review. Participate in clinical research and contribute to scholarly publications and medical conferences. Educate and mentor medical students, residents, and healthcare professionals. Collaboration and Consultation: Provide expert consultations to primary care physicians and other specialists. Work collaboratively in multidisciplinary teams to manage complex cases. Maintain open and clear communication with patients, families, and caregivers. Ensure thorough documentation and upkeep of medical records. Qualifications and Skills: Medical degree (MD or DO) from a recognized institution. Completed residency in Internal Medicine and fellowship in Endocrinology. Board certification or board eligibility in Endocrinology. Valid medical license to practice as an Endocrinologist. Strong clinical expertise in managing diverse endocrine disorders. Excellent communication and interpersonal skills. Empathetic approach to patient care with a focus on education and support. Detail-oriented with solid analytical and diagnostic abilities. Effective team player in multidisciplinary healthcare settings. Commitment to continuous learning and professional development. Proficiency in electronic medical record (EMR) systems.

We are a community based private clinic based at Kundara, Kollam looking for speciality or superspecialty doctors with some experience who wish to run their OP for part time 1 to 3 hours either during morning time or evening time Monday to Saturday once or twice a week. You can charge your OPD consultation fees preferable 200 to 250 (Max 300) Rs per patient and timing each week you can decide as per your convenience.This could be an additional income for you, if you are already working in other hospitals. Preferably looking for doctors in specialties like Allergy and Pulmonology, Cardiology, Neurology, Nephrology, Endocrinology, Gastroenterology, Speech therapy, Child Psychology, Gynaecology,, Dermatology and Cosmetology, or any other relevant specialty. We will provide OPD space and will add a reasonable small charge to each consultation. Clinic might be open hopefully in in 2 to 3 months time, when the consultations will start... But please feel to post your CVs directly to 8590273624 whatsapp... Selected doctors will be contacted in due time. Timings will be flexible as per your convenience. Job Types: Full-time, Part-time Pay: From ₹200.00 per month Education: Doctorate (Preferred) Experience: Physician: 1 year (Preferred) total work: 1 year (Preferred) Work Location: In person

*Please note this role is not for 2070 Health* About Decimal Health Decimal.Health is a boutique digital health innovation consultancy and venture studio. We are a clinician-led company with over two decades of experience in digital health. As consultants we craft bespoke strategies for clients in the healthcare sector, and as a studio we spine out companies - from research labs of a hospital to commercial ventures with a hospital. We pride ourselves on our nimble approach that connects strategy with action, going deeper than traditional consulting firms by leveraging our real-world experience to ensure practical and impactful solutions. Our Life Sciences Advisory & Internal Studio team partners with pharmaceutical and medical device companies, as well as innovative digital health startups, to navigate the journey from strategy to successful market implementation. Through our proven frameworks and deep understanding of stakeholder dynamics, we bridge the gap between innovation and real-world adoption in US healthcare. Role Overview Were seeking a passionate and experienced Consultant to join our Life Sciences Advisory & Internal Studio team. In this role, youll collaborate with pharmaceutical, medical device, and digit

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com. Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization. Brief Team/department Description Our Supply Chain team at Azurity is growing, and we’re looking to strengthen it with passionate and driven team member. If you're eager to be part of a dynamic, global, and fast-growing organization—where a positive mindset, personal development, and making a meaningful impact on people’s health are valued—we could be the perfect match. As Senior Supply Planner, you’ll collaborate across departments and play an active role in shaping the future of our company. Principle Responsibilities Create and maintain the supply plan for CMOs on monthly basis considering the inventory, open orders (firmed and planned) to identify and communicate status to internal and external stakeholders. Based on supply plan, issue Purchase Orders and forecast to CMOs, monitor the deliveries of purchase orders according to requested dates. Proactively manage supply constraints to minimize the business impact. Provide accurate and complete supply planning parameters & purchasing conditions for all SKUs, act as the Expert User for the key planning Master Data. Set and maintain all required Master Data and ensure its integrity and correctness. Create and maintain a strong working relationship with internal and external partners. Oversee the successful launch of new products into the market, ensuring timely supply, regulatory compliance, and effective coordination with manufacturing and distribution teams. Propose stock holding levels within supply chain through a detailed understanding of the key planning parameters and E2E process (safety stock, lead times, supply reliability, demand variability, service objectives) and in line with Working Capital targets. Perform monthly inventory reconciliations and ensure inventory accuracy and minimize discrepancies. Qualifications And Education Requirements Bachelor’s degree in Supply Chain Management or a related field. Minimum of 3 years of relevant experience in Planning, Operations, or Manufacturing, including direct interaction with Contract Manufacturing Organizations (CMOs). Demonstrated ability to work in a fast-paced environment with shifting priorities and evolving business needs. Prior experience in the pharmaceutical industry is preferred. Familiarity with Oracle ERP systems; functional knowledge is an advantage. Strong analytical and problem-solving skills, with excellent communication abilities. Proven track record of effective collaboration with both internal cross-functional teams and external partners. Strong time management skills with the ability to prioritize tasks efficiently. Quick learner with a proactive and adaptable mindset By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.

Neurologist Required at Bathinda Punjab Salary 5 Lakhs Varanasi UP Salary 4 Lakhs Doctor couple can be adjusted in their respective branch

General & Laparoscopic Surgeon Required at Gohana Haryana Salary 3.5 to 4 Lakhs + Accommodation Ambedkar Nagar UP Salary 3.5 Lakhs + Gadchiroli Maharashtra Peripheral Location Salary 3.5 Lakhs + Accommodation + Food Required Candidate profile Veraval Gujarat Salary 3 Lakhs + Accommodation Doctor couple can be adjusted in their respective branch

Job Title: Endocrinologist Location: Apollo Sugar Clinic, Nashik, Maharashtra Job Description: Seeking a qualified Endocrinologist to manage diabetes, thyroid, hormonal, and metabolic disorders with a patient-centric approach. Qualifications: DM/DNB in Endocrinology Valid medical registration/license Strong clinical expertise and patient communication skills

Job Title: Endocrinologist Location: Apollo Sugar Clinic, Nashik Job Type: Full-time Salary- Can be Discussed. Job Summary: We are seeking a highly skilled and experienced Endocrinologist to join our team at Apollo Hospital in Nashik. The Endocrinologist will diagnose and treat patients with endocrine disorders, including diabetes, thyroid disorders, and hormonal imbalances. The ideal candidate should have a strong clinical background, excellent communication skills, and a commitment to providing the highest quality of patient care. Key Responsibilities: Diagnose and treat patients with endocrine disorders, including but not limited to diabetes, thyroid disorders, adrenal disorders, and hormonal imbalances. Conduct comprehensive patient evaluations, including medical history, physical examinations, and laboratory tests. Develop and implement individualized treatment plans for patients based on their specific conditions and needs. Educate patients about their conditions, treatment options, and self-management strategies. Work closely with other medical professionals, including nurses, dietitians, and other specialists, to provide holistic patient care. Maintain accurate and complete patient records in compliance with hospital policies and relevant regulations. Qualifications: Medical degree (DM OR DNB ) with specialization in Endocrinology and Diabetes metabolism. Valid medical license to practice as an Endocrinologist in the state of Maharashtra. Experience in diagnosing and treating endocrine disorders. Strong communication and interpersonal skills. Ability to work well in a team and collaborate with other healthcare professionals. Commitment to providing high-quality patient care. Job Types: Full-time, Permanent, Part-time Pay: ₹100,000.00 - ₹400,000.00 per month Schedule: Day shift Evening shift Morning shift Application Question(s): DM or DNB in endocrinology is mandatory , have you completed the course ? Application Deadline: 25/07/2025 Expected Start Date: 25/07/2025

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com. Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization. Brief Team/department Description We are seeking a motivated and detail-oriented Data Analyst to join our dynamic Supply Chain team. This is an exciting opportunity to contribute to critical decision-making by leveraging data to optimize our supply chain. You will be involved in building data processing models, developing dashboards and generating insights that directly impact efficiency, cost-effectiveness, and the timely delivery of life-saving medications. Principle Responsibilities Assist in the collection, cleaning, and preparation of datasets from various sources relevant to supply chain operations (e.g., demand forecasts, inventory levels, master data). Develop and maintain data processing methods using appropriate tools and technologies (advanced excel, PowerBi, DAX language) to ensure data quality and accessibility. Create and maintain dashboards and visualizations using Power BI and Microsoft Tools (Microsoft Lists, Power Automate, etc). Collaborate with the Supply Chain team to understand business needs and translate them into analytical requirements. Support ad-hoc data analysis requests and contribute to the generation of reports to support decision-making. Drive continuous improvement of business processes, related reports, and metrics. Support the team in leading edge thinking to identify future opportunities in Systems, Tools and Processes. Qualifications And Education Requirements Bachelor’s degree in data science, Statistics, Supply Chain Management, Computer Science, Engineering or a related discipline. Proficiency in DAX programming language and use of Microsoft Suite (Lists, Power Automate, Flows & Forms). Strong analytical and problem-solving skills with the ability to interpret complex data. Strong attention to detail and a commitment to data accuracy. Basic understanding of Supply Chain in the Pharmaceutical industry and inventory management Familiarity with forecasting techniques and inventory optimization concepts is a strong advantage. By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.

*Please note this role is not for 2070 Health* About Decimal Health Decimal.Health is a boutique digital health innovation consultancy and venture studio. We are a clinician-led company with over two decades of experience in digital health. As consultants we craft bespoke strategies for clients in the healthcare sector, and as a studio we spine out companies - from research labs of a hospital to commercial ventures with a hospital. We pride ourselves on our nimble approach that connects strategy with action, going deeper than traditional consulting firms by leveraging our real-world experience to ensure practical and impactful solutions. Our Life Sciences Advisory & Internal Studio team partners with pharmaceutical and medical device companies, as well as innovative digital health startups, to navigate the journey from strategy to successful market implementation. Through our proven frameworks and deep understanding of stakeholder dynamics, we bridge the gap between innovation and real-world adoption in US healthcare. Requirements Role Overview We're seeking a passionate and experienced Consultant to join our Life Sciences Advisory & Internal Studio team. In this role, you'll collaborate with pharmaceutical, medical device, and digital health companies to develop and execute transformative digital health strategies. You'll be part of a team that shapes how innovative solutions reach and positively impact patient care. Key Responsibilities Execute and contribute to strategic life sciences advisory engagements (60-70% of role), incl.: Digital health strategy development for life sciences companies (pharma, biotech, medical device) and digital health companies aiming to partner with life sciences companies Partnership strategy and initiation support Market analysis and opportunity assessment Stakeholder engagement & workshop facilitation with clinical, commercial, and digital teams Support internal studio initiatives (20-30% of role) focused on creating scalable solutions Participate in development of methodologies and frameworks for digital health adoption Collaborate with cross-functional teams across US and India offices Contribute to thought leadership initiatives and business development activities Support client relationship management and project delivery primarily life sciences companies Qualifications Master's degree required (PhD is a plus) in one of the following: Business/related field with 4-5+ years healthcare advisory experience Medical/Life Sciences with 4-5+ years business advisory experience Demonstrated expertise in healthcare consulting or life sciences industry Strong understanding of US digital health landscape and healthcare innovation Experience in therapeutic areas such as oncology, neurology, rare diseases, or endocrinology is highly valued Excellent analytical, strategic thinking, and problem-solving skills Outstanding communication and presentation abilities, with high proficiency in English Experience working with global teams across time zones Proven ability to manage complex projects and stakeholder relationships Genuine passion for improving healthcare through innovation What sets this role apart: unique learning & impact opportunities Navigate the fascinating complexity where clinical science, digital innovation, and business strategy converge See your strategic recommendations transform into real-world solutions that improve patient outcomes Work alongside seasoned healthcare innovators who've led transformations at leading US health systems Collaborate with digital innovators, clinical leaders, and business strategists in a single week Gain unparalleled insights into digital health innovation through our position at the intersection of pharma, health systems, and startups Build relationships with decision-makers shaping the future of healthcare delivery Contribute to shaping not just client solutions, but Decimal's own evolution as we grow What We're Looking For Beyond the qualifications listed above, we seek individuals who bring: Natural curiosity and humility to tackle complex healthcare challenges Ability to thrive in ambiguity and drive impact in a growing organization Self-directed problem-solving balanced with strong team orientation Clear communication and relationship-building skills Passion for healthcare innovation with a commitment to excellence without ego Benefits Team environment You'll be joining a collaborative team that: Values thoughtful discourse and evidence-based decision making Embraces both strategic thinking and pragmatic execution Maintains high standards while supporting each other's growth Focuses on meaningful impact over internal politics Celebrates collective wins and learns together from challenges Location Remote, India What We Offer Opportunity to shape the future of healthcare through digital innovation Work with leading pharmaceutical, medical device companies, and innovative startups Collaborative, mission-driven environment Professional development and growth opportunities Competitive compensation package

The role of the Medical Office is to bring medical, regulatory, scientific and drug safety related insights and expertise to ADVANZ PHARMA and to be subject matter experts across the following functional areas: global regulatory affairs, global medical affairs, global healthcare compliance, global patient safety and global clinical development. This entails engaging and collaborating with regulatory agencies, healthcare organizations, healthcare professionals and customers both internal and external - and generating and communicating relevant, meaningful, and impactful data, and securing and maintaining marketing authorizations across the ADVANZ PHARMA portfolio. In so doing, the Medical Office represents the voice of the patient in all matters; works to ensure that products and marketing authorizations are supported by relevant, up to date data and retain a positive benefit/risk profile; helps to drive our scientific credibility and reputation as a company; enables stakeholders to make informed choices for patients; operates with due regard to all relevant regulations and compliance requirements. About the Role As ADVANZ PHARMA continues to strengthen its position as the partner of choice for specialty, hospital, and rare disease medicines, we have an exciting opportunity for Specialist Regulatory Affairs LCM Strategic Growth Products. Main purpose of the job is to ensure adequate and prompt life cycle maintenance activities for Marketing Authorization s (MA) held by ADVANZ PHARMA based on portfolio assigned with a focus on supply continuity and compliance with regulatory requirements. Provide supportive role to New Product Introduction team during Translation and Product label/mock up finalization to secure necessary approvals. In case of DCPs, responsible for managing the national phase procedure with respective health authorities. Become the primary point of contact for Health Authorities following grant of Marketing Authorisation; as we'll become the single point of contact for the organization. This role will shadow the New Products Introduction Manager (Product Lead) to seek necessary knowledge of the new MA procedure and all the HA interactions that occurs during this procedure with an intent to identify specific negotiations, key commitments made and also identify potential post approval activities that might be necessary to either support a product launch or maintain continuity of supplies. This role will start working with NPI function, necessary stakeholders internal (such as Quality, Supply Chain, Technical, Medical or Commercial) and external (such as developer) to plan, strategize and execute all necessary post approval activities which will include but not limited to the following: Renewal Application and Annual Maintenance Variation Application Notification of Change in Marketing Status, sunset clause exemptions where applicable Notification of drug shortages Tracking and fulfillment of regulatory commitments made including any Specific Obligations for Conditionally /Exceptionally approved products. PIP Modifications, PIP compliance and associated label update Orphan Designation Maintenance (where applicable) Updation of NBO technical package (where applicable) This role will be assigned specific molecules, Primarily Innovative Medicines (but may as we'll extend other categories) and will become the LCM product lead for the assigned molecules globally, in all markets where there are registrations/Marketing Authorization available. This role will be expected to maintain and discuss/align Regulatory submission Plan, Regulatory Post Approval Strategy with cross functional teams. This role will be nominated to be involved being part of cross functional meetings such as Change Control Meeting, SNOP meeting etc for their assigned molecules. This role will be supported by Subject Matter Experts from the New Products Team (for Biosimilars and Specialty Generic Products) and Innovative Medicines team (for NCE and Biologics) for strategy formation and review. This role hence should be able to collaborate and work very closely with these functions throughout the life cycle of the products. This role will also contribute to the preparation of meeting packages for Scientific Advice, as and when needed and drive readiness preparation and participate in scientific advice as may be necessary to determine any post approval regulatory strategy. This role will support any market expansion activity by either driving or supporting a new product application of assigned molecules (already approved in EU, UK) to newer territories. This will be decided on a case-by-case basis. This role will be also responsible for maintaining Hand over document that would be used for further transition of responsibilities to LCM Established Products at a later stage for Innovative Medicines and Specialty Generic Products. While, ideally responsibilities of any approved products acquired through M&A will not sit with this role, howe'ver, depending on the nature of the products acquired, this role may be involved and become responsible for due diligence and integration. For example, any asset which is a Conditional Marketing Authorisation or has an Exceptional Circumstances status at the time of acquisition, would best sit with the LCM Strategic Growth team. Actively participate in continuous improvement initiatives, share ideas and thoughts, actively involve in implementation of such initiatives. Act as process owner for some regulatory procedures as and when delegated. Support line managers for readiness of any health authority inspection as and when delegated. Ensure timely completion of assigned Deviation and CAPAs. We are looking for highly motivated individuals who are passionate about making a meaningful difference to patients lives. For this role, you will also have the following: Qualifications: Graduate or post-graduate in any discipline of Science, preferably life science / Pharmacy. Knowledge, Skills & Experience: Significant experience of handling life cycle management of pharmaceuticals in EU/UK and other regulated markets (such as Canada, Australia and New Zealand) as an individual contributor. Good understanding of ICH Clinical and Safety guidelines should be able to interpret guidelines and apply them in practical situations independently we'll versed with EU/UK Regulatory procedures and processes. Good understanding and hands on experience of working on CTD. Experience interacting with EU/UK regulatory authorities Scientific advice meetings/ Pre-submission meetings. Experience of handling Innovative Medicines post approval changes such as PIP modifications and label expansions. Hands on experience of document management and change control management systems. Strong Project Management and Communication skills. Pleasant personality with collaborative approach, strategic mindset & Positive attitude. Demonstrate sense of drive and urgency through work. Be able to take decisions based on facts available, trend and suggest solutions to line manager (solution oriented). Excellent communication skills verbal and written; Ability to present to senior stakeholders confidently Ability to work under pressure and flexibility to adapt to evolving business situation. Inspired by our values of entrepreneurship, speed and integrity. Learning agility and scalability , with a desire to continuously improve and develop as ADVANZ grows. Work collaboratively across all business functions with an open, honest, and respectful cooperation. Ability to have fun and thrive in a growing, unique, and inclusive work environment.

ENDOCRINOLOGIST JOB IN PALAKKAD, KERALA, INDIA Designation: CONSULTANT ENDOCRINOLOGIST Qualification: MD., DM Endocrinology 0 To 3years Experienced Male or Female Malayalam speaking Doctors preferred Duty Time: 8Hrs duty Type of Duty: OP/IP/ICU

ENDOCRINOLOGIST JOB IN PALAKKAD, KERALA, INDIA Designation: CONSULTANT ENDOCRINOLOGIST Qualification: MD., DM Endocrinology 0 To 3years Experienced Male or Female Malayalam speaking Doctors preferred Duty Time: 8Hrs duty Type of Duty: OP/IP/ICU

About Gini Health: Gini Health is a 24/7 advanced care hospital with ICU and emergency services, offering top-quality care in internal medicine, endocrinology, and critical care. We're led by a team of India’s most respected doctors, including Dr. Anil Bhansali, former HOD of Endocrinology at PGIMER Chandigarh. From managing complex IPD and ICU cases to offering cutting-edge outpatient diagnostics and chronic care, Gini is setting a new standard for patient-centric, outcome-driven healthcare in North India. We’re not just treating illness, we’re building a system of prevention, rapid response, low readmission, and compassionate care. The Opportunity: We are hiring full-time Medical Officers (MBBS) to be part of our expanding IPD and ICU team in Mohali. You will work directly with specialists gaining hands-on experience in both acute and chronic patient management. You’ll play a key role in managing ICU and IPD admissions, supporting emergency and OPD care, and using EMR, structured protocols, and data to deliver superior outcomes. Key Responsibilities: Manage IPD/ICU rounds, patient admissions, and shift duties Monitor vitals, coordinate with consultants, and implement treatment plans Support in OPD consultation and emergency walk-ins Maintain and update Electronic Medical Records (EMR) accurately Conduct patient and family counselling regarding treatment, recovery, and follow-up Participate in regular team huddles, audits, and quality care discussions Eligibility: MBBS with 1–5 years experience in hospital (IPD/ICU preferred) Solid clinical judgment and willingness to take initiative Proficient with digital records and hospital workflows Strong communicator with empathy and teamwork skills Why Join Gini? Learn from a world-class team of doctors and specialists Hands-on experience in critical care, internal medicine, and endocrinology Exposure to new-age hospital protocols, patient journey mapping, and outcome measurement Fast-growing environment with opportunities for career advancement and research

The clinical embryologist must be knowledgeable in mammalian embryology, Reproductive endocrinology, genetics, molecular biology, biochemistry, Microbiology and in vitro culture techniques. The embryologist must also be familiar with ART. Qualification: A medical graduate or have a postgraduate degree or a doctorate in an appropriate area of life sciences. (In the case of a clinic in existence for at least one year before the promulgation of these rules, a person with a B.Sc. or BVSc degree but with at least three years of first-hand, hands-on experience of the techniques mentioned below and of discharging the responsibilities listed below, would be acceptable for functioning as a clinical embryologist. Such persons would also be eligible to take a test to be designed and conducted by an appropriate designated authority.) He / she must be familiar with the following: Principles and practice of semen analysis and cryopreservation of semen. Cytology of mammalian and human oocyte to identify stages of oocyte maturation accurately . All aspects of embryology including developmental biology. Cell biological techniques used in cell and tissue culture. Molecular biology and genetics of human reproduction. Micromanipulation of sperm and oocytes for carrying out ICSI and single-cell biopsies of embryos for preimplantation genetic diagnosis. Principles and functioning of all the equipment used in the laboratory. In vitro fertilization of oocytes after processing the gametes. Principles and practice of embryo freezing. The responsibilities of the clinical embryologist would be: To ensure that all the necessary equipments are present in the laboratory and are functional. To perform all the procedures pertaining to processing, handling and culturing of gametes and embryos in the laboratory and hand over the embryo to the gynaecologist. To maintain records of all the procedures carried out in the laboratory. Essential: Qualification: Medical graduation / Post graduation degree. Experience – min 3 years exp in clinical embryology. Job Type: Full-time Work Location: In person