8 internal Medicine Jobs nearby Pune

As an experienced and motivated Adjunct Faculty member with a strong background in medicine, nutrition, or related life sciences, your role will involve supporting content development and academic writing. This fully remote position offers flexibility while contributing to the creation of high-quality educational materials, research summaries, and scientific communications. Ideally suited for fresh MBBS graduates preparing for their MD, PhD students, or fresh PhDs in specialities listed below in qualifications. **Key Responsibilities:** - Develop educational content for courses, workshops, and publications in the fields of nutrition, exercise science, molecular biology, and allied health. - Write, edit, and review scholarly articles, research summaries, and academic materials. - Ensure scientific accuracy, clarity, and adherence to academic standards in all written materials. - Collaborate virtually with faculty, researchers, and instructional teams to translate complex concepts into accessible content. - Stay updated with recent research and advances in relevant fields to inform content creation. **Required Qualifications:** - MBBS. - MD specialities - Path, Internal Medicine, OB-GYN, Paediatrics, Family Medicine, Preventive Healthcare, Community Medicine, Physical Therapy, Sports Medicine, Public Health, Endocrinology. - PhD in Nutrition, Exercise Science, or related discipline. - Proven track record of academic publications in peer-reviewed journals. - Demonstrated experience in academic writing, scientific communication, or content development. - Strong command of scientific writing standards, referencing, and ethical research reporting. **Preferred Skills:** - Experience in curriculum or educational content development. - Ability to simplify complex scientific concepts for diverse audiences. - Familiarity with digital content tools and platforms for academic publishing. In addition to the above, there are multiple positions available for this fully remote role, offering flexibility in work location and hours. If you are interested and suitable for the role, please send your resume and cover letter to career@fittr.com with the subject line: Application for (Position Name) (Your Name).,

Role Overview: As an Associate Specialist in Data Visualization at our Human Health Division, you will be pivotal in developing compelling data visualization solutions to enable actionable insights and facilitate intuitive information consumption for internal business stakeholders. Your role will involve collaborating with various teams to create user-centric visuals and dashboards, empowering stakeholders with data-driven insights and decision-making capabilities. Key Responsibilities: - Develop user-centric scalable visualization and analytical solutions using complex data sources to create intuitive and insightful dashboards. Apply best practices in visualization design to enhance user experience and business impact. - Collaborate with Data Viz leads and stakeholders to define key metrics, KPIs, and reporting needs. Participate in workshops to develop user stories, wireframes, and interactive visualizations. - Partner with data engineering, data science, and IT teams to develop scalable business-friendly reporting solutions, ensuring adherence to data governance, privacy, and security best practices. - Identify opportunities for automation and streamline manual reporting processes through modern visualization technologies and self-service analytics enablement. - Ensure timely delivery of high-quality outputs, create and maintain SOPs, KPI libraries, and other essential governance documents. - Continuously innovate on visualization best practices and technologies by reviewing external resources and marketplace trends. Qualifications Required: - 2+ years of experience in business intelligence, insight generation, data visualization, infographics, and interactive visual storytelling. - Hands-on expertise in BI and visualization tools such as Power BI, PowerApps, Qliksense, MicroStrategy, and ThoughtSpot. - Experience in data engineering and modeling, including ETL workflows, Dataiku, Databricks, Informatica, and database technologies like Redshift and Snowflake, with programming skills in SQL and Python. - Experience in pharmaceutical commercial analytics, agile ways of working, and good problem-solving and communication skills. - Basic understanding of product management principles, focusing on developing user-centric, scalable analytical solutions aligned with business needs. - Strong learning agility and adaptability to new tools, technologies, and business environments while enhancing analytical and technical skills. Additional Company Details: Our Human Health Division maintains a patient-first, profits-later ideology, comprising sales, marketing, market access, digital analytics, and commercial professionals dedicated to bringing medicines to customers worldwide. We value diversity and inclusivity, encouraging respectful challenges and collective problem-solving. As an equal opportunity employer, we are committed to fostering an inclusive and diverse workplace.,

Role Overview: As the Supervisor of Data Support Operations at our company, you will be responsible for leading a support team to ensure the accuracy, integrity, and regulatory compliance of data processes that support various teams and roles within the Data Operations and Biorepository Support department. Your role will involve managing a team focused on data entry and coordination, optimizing workflows, and enhancing data quality through collaboration with cross-functional teams. Key Responsibilities: - Oversee data modification requests initiated via the Ticketing System. - Manage E-portal requests initiated via the Ticketing System. - Investigate and resolve data discrepancies in collaboration with project collaborators. - Review and validate supporting documentation and mapping files for data changes. - Conduct impact assessments to ensure accurate and complete data updates. - Coordinate with requestors to confirm additional sample updates when necessary. - Create and manage modification batches in BSI with traceability and audit readiness. - Ensure data updates are accurately reflected in inventory systems and communicate resolution status to stakeholders. - Prepare draft correspondence to document actions taken to correct data errors. - Prepare and analyze reports from the BSI to identify potential errors in data. Data Governance: - Train data entry personnel in proper protocol operation as needed. - Manage data entry processes and establish guidelines, training programs, and quality assurance measures. - Collaborate with Biorepository teams to align priorities and streamline workflows. - Drive process improvement initiatives focusing on automation and simplification. - Ensure compliance with Good Clinical Practices (GCP) and relevant regulatory standards. Leadership: - Lead cross-functional and organization-wide initiatives. - Provide training, support, and mentorship to team members. - Foster a collaborative and goal-oriented team culture. - Assign tasks, set expectations, and provide constructive feedback. - Maintain effective communication with internal stakeholders and project teams. - Assess project timelines and resource needs, offering strategic input. Qualifications: Minimum Requirements: - Minimum 6 years of relevant experience. - At least 3 years in a leadership or supervisory role. - Proficiency in clinical research operations and data management. - Strong understanding of drug, device, and biologic development processes. - Experience with clinical database systems and data quality standards. - Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook). - Excellent organizational, written, and verbal communication skills in English. Preferred Qualifications: - Background in clinical, scientific, or healthcare disciplines. - Familiarity with data privacy regulations (e.g., GDPR, HIPAA). - Experience with Power BI, Power Query, and/or Power Automate. - Knowledge of Laboratory Information Management Systems (LIMS) and Biospecimen Inventory Systems. - Experience using Smartsheet for project tracking and collaboration.,

As a Document Control Specialist at Precision for Medicine, your role involves the maintenance and management of controlled documents and records. You will also provide administrative support to the quality assurance team. Your key responsibilities will include: - Facilitating the electronic document control process for Quality System Documents, ensuring proper document formatting and organization - Collaborating with owners, reviewers, and approvers to ensure right-first-time review and compliance with internal standards - Assisting in Quality Systems Procedure revision during integration processes - Assigning training workflows for new procedures and employees - Maintaining document security and coordinating Periodic Review of Documents - Conducting training for new and existing employees on the electronic quality management system - Locating, reviewing, submitting, and reconciling document/record requests during audits - Ensuring timely response to documentation requests during audits and preparing welcome packet folders for audits - Updating procedure binders and preparing Dossiers on Employees Training Binders Qualifications Required: - Bachelor's degree - 1-3 years of experience with ISO 9001/13485 standards - Working knowledge of quality and documents in a clinical research organization - Document Control certification within the first year - Ability to meet deadlines, proficiency in Microsoft Office suite, and fluency in English language If you require a reasonable accommodation due to a disability or need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.,

As a SAS Programmer at Precision for Medicine, you will play a crucial role in supporting the success of clinical trials through your SAS programming skills. Your responsibilities will include: - Developing and maintaining SAS programming to support the review of clinical data as part of a cross-functional data review and cleaning approach - Providing collaborative input to design SAS outputs for metrics, reconciliation reports, tools, listings, and standard patient profiles - Supporting the development of complex proprietary patient profiles for efficient data review and monitoring - Ensuring on-time delivery of projects, communicating project status to internal teams - Developing, testing, and validating SAS programs for client-related and cross-functional projects - Troubleshooting and resolving SAS program issues - Developing and maintaining SAS programming validation documents - Participating in demonstrations, trainings, and SOP development - Providing leadership for cross-functional initiatives and training project team members - Communicating with study sponsors, vendors, and project teams regarding data and project issues - Conducting software demonstrations, training sessions, and presenting at project meetings Qualifications: Minimum Required: - Bachelor's degree or equivalent in local country or relevant experience - Minimum of 3+ years of experience in clinical, scientific, or healthcare discipline Other Required: - Broad knowledge of drug, device, and biologic development and effective data management practices - Proficiency in Base SAS, SAS/STAT, SAS/ACCESS, SAS Macro Language - Proficiency in Microsoft Office applications - Excellent organizational and communication skills - Experience in utilizing clinical database management systems (EDC) Preferred: - Experience in Object-Oriented Programming, scripting languages, R, SQL - Oncology and/or Orphan Drug therapeutic experience Please note that any data provided as a part of this application will be stored in accordance with Precision for Medicine's Privacy Policy. For California applicants, please refer to the CA Privacy Notice. If you require a reasonable accommodation to complete the application process, please contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.,

As an Assistant Doctor in Ayurveda specializing in skin conditions, your role will involve supporting Ayurvedic doctors in providing care for patients with skin issues, assisting in treatments, and managing patient care. Key Responsibilities: - Assisting in Consultations: - Support Ayurvedic doctors during patient consultations for skin issues. - Help document patient history and treatment plans. - Treatment Assistance: - Assist in administering Ayurvedic treatments such as Panchakarma for skin. - Prepare herbal medicines and oils as per prescriptions. - Patient Care: - Provide basic care and guidance to patients with skin conditions. - Educate patients on diet and lifestyle based on Ayurvedic principles for skin health. - Clinic Management: - Help manage patient records and appointments. - Ensure clinic hygiene and prepare for treatments. Qualification Required: - BAMS (Bachelor of Ayurvedic Medicine and Surgery) qualification is preferable. - Experience in Ayurvedic practice and skin treatments would be beneficial. In this role, your knowledge of Ayurvedic principles, skin disorders, and treatments will be essential. You should also be familiar with herbal medicines and Panchakarma therapies. Good communication skills for patient interaction and attention to detail for treatments and medicines are necessary for success in this position. Additionally, you will be involved in Ayurvedic skin treatments such as Panchakarma, which are cleansing therapies for skin rejuvenation. You will also work with herbal medicines for internal and external applications to address skin issues, as well as provide diet and lifestyle advice based on Ayurveda for skin health. This is a full-time job that requires in-person work at the designated location.,

As a RWE-HEOR-Patient Analytics Specialist at Improzo, you will be responsible for leveraging Patient Analytics, Real-World Evidence (RWE), and Health Economics & Outcomes Research (HEOR) methodologies to drive impactful insights and support life sciences clients in optimizing patient outcomes, decoding patient journeys, and refining healthcare strategies. Your role will involve applying advanced analytical techniques to generate evidence, drive patient-centric insights, influence healthcare decision-making, and support market access strategies. **Key Responsibilities:** - **Patient Journey Analytics & Segmentation:** Lead comprehensive patient journey mapping initiatives, utilizing advanced analytics to identify patient phenotypes, treatment pathways, adherence patterns, and care gaps across diverse therapeutic areas. - **Predictive Patient Modeling:** Develop and deploy machine learning models for patient risk stratification, treatment response prediction, and personalized care pathway optimization using multi-modal healthcare data sources. - **Patient-Reported Outcomes Analysis:** Design and execute sophisticated analyses of patient-reported outcomes (PROs), quality of life measures, and patient satisfaction data to quantify treatment impact from the patient perspective. - **Real-World Data Integration & Patient Cohort Development:** Apply advanced statistical modeling and epidemiological methods to analyze claims data, EMRs, wearable device data, and patient registries with a focus on patient-level insights and longitudinal patient analytics. - **Health Economics Through Patient Lens:** Conduct patient-centered economic evaluations, including cost-per-patient analyses, patient lifetime value modeling, and healthcare resource utilization studies to support value-based care initiatives. - **Advanced Patient Analytics Solutions:** Lead the design and implementation of AI/ML applications for patient behavior prediction, treatment optimization algorithms, and patient engagement analytics to inform precision medicine strategies. - **Client Engagement & Patient-Centric Strategy:** Collaborate with clients to translate patient analytics insights into actionable healthcare strategies, focusing on patient outcomes improvement, care personalization, and patient experience enhancement. - **Project Leadership & Innovation:** Manage complex patient analytics projects end-to-end while fostering innovation in patient data science methodologies and contributing to thought leadership in patient analytics. - **Team Development & Knowledge Sharing:** Mentor team members in patient analytics techniques and contribute to internal capability building in patient-centered research methodologies. **Qualifications:** - **Education:** Bachelor's or Master's degree in Data Science, Biostatistics, Health Informatics, Digital Health, Epidemiology, Health Economics, Public Health, or related quantitative fields with an emphasis on patient-centered research. - **Experience:** 3-9 years of experience in Patient Analytics, Digital Health Analytics, RWE, and HEOR, preferably within the pharmaceutical, consulting, or healthcare industries. **Additional Details:** Improzo is dedicated to improving life by empowering customers through quality-led commercial analytical solutions. The company's core values framework, CARE, emphasizes Customer-Centricity, Adaptability, Respect, and Execution. The collaborative environment at Improzo offers leadership opportunities in cutting-edge patient analytics, RWE, and HEOR initiatives, career development in the rapidly growing field, exposure to innovative healthcare technologies, and professional development support including conferences, certifications, and advanced training in patient analytics, RWE, and HEOR methodologies.,

Role Overview: You will be a Pharmacy Support professional with a minimum of 2 years of experience in prescription reading and a solid understanding of pharmaceutical drugs and medicines. Your role will involve accurately interpreting and processing medical prescriptions, validating prescription details, providing pharmaceutical support to internal teams and clients, handling drug-related queries, maintaining updated records, collaborating with cross-functional teams, and ensuring timely completion of pharmacy-related tasks. Key Responsibilities: - Accurately read, interpret, and process medical prescriptions. - Validate prescription details and ensure alignment with regulatory and clinical guidelines. - Provide pharmaceutical support to internal teams and clients, ensuring clarity and accuracy in drug-related information. - Handle queries related to drug usage, dosage, and side effects as per standard protocols. - Maintain updated records and documentation in accordance with company and regulatory standards. - Collaborate with cross-functional teams including medical, technical, and client support teams when needed. - Ensure timely and accurate completion of assigned pharmacy-related tasks. Qualification Required: - Strong understanding of medications, dosages, therapeutic classes, and pharmacy practices. - Proficient in interpreting handwritten and digital prescriptions. - Familiarity with healthcare IT systems is a plus. - Minimum of 2 years in a pharmacy support, prescription processing, or clinical operations role. - Excellent verbal and written English communication skills. - Ability to clearly document and communicate pharmaceutical information.,

\  Greetings !  We are in Search of Qualified CA for Managing Direct Taxation activities of the Organization:  Company Profile : The multidivisional organization having diversified interests in Ethical Formulations, Bulk Drug, Ayurvedic Medicine, Healthcare, Herbal Products and Bio-technology, seeds andTissue Culture.  Position : Sr. Manager Taxation.  Location : Vile Parle-Mumbai  Qualification : Chartered Accountant(CA)  Experience : Qualified CA with an exposure to Plan , Mange & Control the Direct Taxation activities of the Manufacturing concern, Preferably Pharma.  Job Description 1. Direct Taxation a. Tax Compliance & Return Filing Prepare and file Income Tax Returns (ITR) of the company. Ensure TDS compliance (deduction, deposit, returns 24Q, 26Q). Handle advance tax calculations and timely payments. Reconcile Form 26AS, TDS certificates, and ledger balances.  b. Tax Audits and Assessments Coordinate with auditors for Tax Audit under Section 44AB. Prepare and maintain Tax Audit Report (Form 3CD). Handle Income Tax scrutiny/assessment proceedings, respond to notices, and liaise with tax consultants.  c. Tax Planning & Advisory Optimize tax liability through legal tax planning. Analyze impact of amendments in direct tax laws (Finance Act changes). Guide business decisions with tax cost projections.  2. Personal Accounts (Promoters / Directors / Key Individuals) Managing personal accounts of promoters or directors, responsibilities may include: a. Bookkeeping & Personal Accounting Monitor personal books of accounts of directors/promoters (using Tally, Excel, or similar tools). Track investments, assets, liabilities, and cash flows.  b. Personal Tax Compliance File personal Income Tax Returns. Manage HUF accounts, capital gains, rental income, and interest/dividend tracking.  3. Internal Controls & Coordination Ensure compliance with internal financial controls. Coordinate with statutory auditors, internal auditors, and tax consultants. Manage tax records and ensure data is audit-ready.  4. MIS and Reporting Prepare tax-related reports for management (monthly, quarterly). Maintain tax liability schedules, contingent liabilities, and tax provision working. Support in Board presentations or reports related to taxation and personal accounts.  5. Other Duties Assist in GSTR-9/9C reconciliation Keep up with CBDT circulars, case laws, and notifications. Training junior accountants on direct tax matters.  Interested Candidates with relevant experience, please share your updated CV on smartopening@gmail.com along with following summary: Current Organization: Current Location: Exposure to Direct Taxation (Years) Exposure to Finalization & Financial Reporting (Years) Present CTC Expected CTC Notice Period  Regards Asha You may speak with P R Sawant on 8355998309 Please share this mail with your colleague, friend, having required exposure & looking out for change.

You will be responsible for underwriting management and ensuring compliance with regulatory guidelines. Your key responsibilities will include: - Underwriting cases at an average of 30 medical or 45 non-medical cases per day. - Performing quality checks at an average of 50 medical and 65 non-medical cases per day. - Scrutinizing all documents for completeness and verifying supporting evidence. - Carrying out risk assessment and approving cases if all requirements are met, or requesting further information if needed. - Making decisions on both standard and non-standard cases. - Coordinating with other departments to ensure completeness of decisions. - Adhering to predefined quality parameters and underwriting philosophy. In terms of compliance, you will need to: - Ensure compliance with IRDA guidelines, internal guidelines, and ISO requirements. - Identify any gaps and implement measures for gap resolution. - Maintain acceptable audit ratings in all compliance and audit reviews. - Assist in internal/external audits and closure of audit reports. Qualifications required for this role include: - Graduation/Post Graduation in Science/Pharmacy/Medicine/Life Science/Microbiology. - Minimum 6 months to 2 years of related experience. - Good technical knowledge of Life underwriting, including Protection Underwriting. Desired qualifications include: - Underwriting and related technical certifications like AALU, ALMI, and MBA/Diploma in Insurance. - Strong business writing skills and ability to make effective presentations. - Knowledge of Insurance business and Financial services operations. Please note that this role is for the position of Executive & Sr. Executive Medical Underwriter in the Healthcare & Life Sciences department.,

As an Associate Consultant in Critical Care at one of the reputed hospitals in Mumbai, your role will involve delivering high-quality critical care services in alignment with hospital protocols and standards. You will be responsible for patient management in the ICU, leading clinical rounds, coordinating with multidisciplinary teams, ensuring adherence to quality benchmarks such as NABH and JCI, mentoring junior staff, and participating in research and innovation activities. **Key Responsibilities:** - Manage ICU admissions, interventions, and treatment plans - Ensure compliance with hospital protocols and patient safety standards - Collaborate with intensivists, specialists, and nursing teams - Monitor patient progress, documentation, and ensure timely discharges - Contribute to quality initiatives, audits, and infection control - Participate in teaching, training, and clinical research activities **Qualifications Required:** - MBBS with MD/DNB in Internal Medicine, Anesthesia, or Chest Medicine - Minimum 5-7 years post-PG experience, with at least 4-5 years in a critical care setup - Additional certifications preferred: DM/DNB in Critical Care, ISCCM Fellowship, European Diploma in Intensive Care, ACLS, ATLS If this opportunity excites you, please share your CV with priyanka.r@hireindians.com and contact us at +91 79821 32501.,

As a Regulatory Affairs Associate II at Teva Pharmaceuticals, your role involves preparing and revising high-quality US Gx labeling documents submitted under an ANDA and/or 505(b)(2). Your responsibilities include ensuring compliance with federal regulations, guidance documents, and internal procedures while meeting deadlines aligned with company objectives. Key Responsibilities: - Develop US labeling documents to align with company goals and submission requirements for assigned ANDAs and/or 505(b)(2)s, ensuring compliance with all legal and regulatory requirements. This involves QC, proofing, editing, and formatting of documents, as well as coordinating the review and approval of final submission documents. - Create compliant Structured Product Labeling (SPL) files, ensuring complete drug listing information and adhering to compliance requirements for importation, bulk listings, and related processes. - Establish and maintain SPL for assigned projects, ensuring product data elements align with required drug listing regulations and are submitted through FDA's Electronic Submission Gateway. - Prepare and compile full responses to the FDA via the appropriate filing mode, including side-by-side comparisons, SPL, and other necessary submission materials. - Perform quality reviews of labeling and submission documents by proofreading established files for content accuracy. - Work closely with external departments and Regulatory Operations to align with internal product/device strategy and process. - Attend project meetings to ensure labeling timelines are met and maintain an accurate project tracker for all assigned projects. Qualifications Required: - Bachelors in Pharmacy/Master in Science & Life Sciences with 4-5 years of experience in the Pharmaceutical Industry, or Master in Pharmacy with 3-4 years of experience. - Proven experience in regulatory affairs within the pharmaceutical, biotechnology, or medical device industry. - Ability to multi-task in a fast-paced work environment and possess exemplary oral and written communication skills. - Organized with keen attention to detail, ability to work independently as well as in a team environment with minimal supervision. - Knowledge of US FDA regulations and guidances related to US Gx labeling, US drug listing, and eCTD submission standards. - Proficiency in PC, Microsoft Office Suite, Microsoft Word, Microsoft Excel, and Adobe Acrobat Professional. Please note that this role offers you the opportunity to work with the world's leading manufacturer of generic medicines, contributing to the mission of making good health more affordable and accessible to millions around the world. Join us in our commitment to making a difference in global healthcare. As a Regulatory Affairs Associate II at Teva Pharmaceuticals, your role involves preparing and revising high-quality US Gx labeling documents submitted under an ANDA and/or 505(b)(2). Your responsibilities include ensuring compliance with federal regulations, guidance documents, and internal procedures while meeting deadlines aligned with company objectives. Key Responsibilities: - Develop US labeling documents to align with company goals and submission requirements for assigned ANDAs and/or 505(b)(2)s, ensuring compliance with all legal and regulatory requirements. This involves QC, proofing, editing, and formatting of documents, as well as coordinating the review and approval of final submission documents. - Create compliant Structured Product Labeling (SPL) files, ensuring complete drug listing information and adhering to compliance requirements for importation, bulk listings, and related processes. - Establish and maintain SPL for assigned projects, ensuring product data elements align with required drug listing regulations and are submitted through FDA's Electronic Submission Gateway. - Prepare and compile full responses to the FDA via the appropriate filing mode, including side-by-side comparisons, SPL, and other necessary submission materials. - Perform quality reviews of labeling and submission documents by proofreading established files for content accuracy. - Work closely with external departments and Regulatory Operations to align with internal product/device strategy and process. - Attend project meetings to ensure labeling timelines are met and maintain an accurate project tracker for all assigned projects. Qualifications Required: - Bachelors in Pharmacy/Master in Science & Life Sciences with 4-5 years of experience in the Pharmaceutical Industry, or Master in Pharmacy with 3-4 years of experience. - Proven experience in regulatory affairs within the pharmaceutical, biotechnology, or medical device industry. - Ability to multi-task in a fast-paced work environment and possess exemplary oral and written communication skills. - Organized with keen attention to detail, ability to work independently as well as in a team environment with minimal supervision. - Knowledge of US FDA regulations and guidance

As a Quality Review Specialist at Fortrea, your role involves ensuring the delivery of high-quality service to both internal and external clients in a safe and cost-effective manner. You will be responsible for complying with various legal requirements related to health and safety regulations. Key Responsibilities: - Perform quality review of assigned cases and compile quality metrics to identify trends. - Address periodic client quality reviews and assist in preparing corrective and preventive actions. - Ensure implementation of Corrective and Preventive Action (CAPA) results in coordination with project managers. - Review various cases and safety reports for global regulatory submissions. - Manage and review adverse events, product quality complaints, and medical information to required standards. - Assist in process reviews, training schedules, and process improvement initiatives. - Respond to medical information queries and product quality complaints via various communication channels. - Execute drug safety data management processes and guide safety associates as required. - Perform any other support activities as assigned, such as tracking information, ongoing quality control, and reconciliation of data. Qualifications Required: - Bachelors/Masters/PhD degree in relevant fields such as Medicine, Pharmaceutical Sciences, Life Sciences, etc. - Relevant work experience of at least two years in the pharmaceutical industry, with a focus on Pharmacovigilance/Safety writing. - Knowledge of medical terminology, Good Clinical Practice (GCP), ICH Guidelines, and worldwide regulatory requirements. - Proficiency in Microsoft Office applications. Preferred Qualifications: - Experience in generating quality metrics, authoring Corrective and Preventive Action Reports. - Knowledge of Medical Device reporting. Physical Demands/Work Environment: - Office Environment with occasional travel as necessary. Please note that Fortrea may consider relevant experience in lieu of educational requirements. If this opportunity aligns with your expertise and career goals, we encourage you to apply and become a valuable part of our team.,

As a member of the Customer Care Team at Kuehne+Nagel, you will contribute to the delivery of customer excellence by developing and diversifying business in alignment with financial and volume targets. Your impact will be felt through various activities that focus on enhancing sales activities, fostering customer relationships, and ensuring high levels of service quality. Your collaboration with internal and external stakeholders will be crucial in achieving the following key objectives: - Own, monitor, and drive all sales activities for customers within your control, from preparing quotations to closing profitable deals. - Align sales efforts with CCL managers, pricing, and business development teams. - Monitor competition by gathering marketplace information on pricing and products. - Report customer feedback to the CCL team and support resolutions as necessary. - Align with CCL colleagues during the onboarding of new customers. - Maintain and update relevant customer information in internal systems. - Regularly review customer portfolios with CCL Managers and the team. - Focus on customer engagement, satisfaction, retention, and reactivation through high service quality. To excel in this role, you should bring: - Experience in sales within logistics, freight forwarding, or sea logistics. - Ability to identify, qualify, and convert prospects through a structured sales pipeline. - Skills in preparing accurate customer quotations and supporting pricing decisions. - Knowledge of market trends, competitor activity, and customer needs. - Strong collaboration skills with CCL managers, pricing, and business development teams. - Customer-focused mindset with experience in onboarding, engagement, satisfaction, and retention. - Ability to maintain updated customer information in internal systems. - Strong organizational and communication skills. - Proven ability to drive profitable and sustainable business growth. Joining Kuehne+Nagel will offer you the following benefits: - Global Industry Leader: Work for one of the top logistics and supply chain companies worldwide. - Career Growth Opportunities: Access strong internal development programs, training, and global mobility. - Diverse & Inclusive Culture: Collaborate with teams across the globe in a supportive and multicultural environment. - Innovative & Future-Focused: Be part of a company investing in sustainability, digitalization, and green logistics. - Competitive Benefits: Enjoy attractive compensation, flexible working options, and comprehensive benefits packages. At Kuehne+Nagel, your work extends beyond logistics to impact the lives of people worldwide through the delivery of essential goods and services. As a global leader committed to moving the world forward, we offer a safe and stable environment where your career can truly make a difference. Whether you are helping deliver life-saving medicines, developing sustainable transportation solutions, or supporting local communities, your contributions will be more significant than you can imagine.,

Job description Roles and Responsibilities Provide high-quality patient care to patients with various medical conditions, including acute and chronic illnesses. Conduct thorough physical examinations, take medical histories, and order diagnostic tests as needed. Develop treatment plans for patients based on their individual needs and medical history. Collaborate with other healthcare professionals to ensure comprehensive care for patients. Stay up-to-date with latest medical research, guidelines, and best practices in internal medicine. Desired Candidate Profile 0-5 years of experience in general medicine or related field. Medical-MS/MD degree from a recognized institution. Strong knowledge of general medicine principles, diagnosis, and treatment options.

Medicine Specialistdiagnoses and treats a wide range of diseases and conditions, primarily in adults. Key responsibilities include conducting physical exams, interpreting diagnostic tests, developing and implementing treatment plans, prescribing medication, and collaborating with other healthcare professionals. They must also maintain accurate patient records and stay current with medical advancements through continuous learning. Core responsibilities    Patient care: Conduct thorough physical exams and patient interviews to diagnose and manage a wide range of medical conditions.    Treatment planning: Develop and implement personalized treatment plans, which may include prescribing medications, therapies, or surgical referrals.    Diagnostics: Order and interpret laboratory tests, imaging studies, and other diagnostic procedures to inform diagnoses.    Collaboration: Work closely with other healthcare professionals, such as nurses, specialists, and other physicians, to provide comprehensive and holistic care.    Communication: Clearly explain diagnoses, treatment options, and potential side effects to patients and their families.    Documentation: Maintain accurate and confidential patient records, including medical history, treatment plans, and progress notes.    Professional development: Stay up-to-date with the latest medical research, advancements, and best practices in internal medicine.    Preventative care: Advise patients on healthy habits and preventative measures to promote overall healthRequired qualifications    Doctor of Medicine or degree from an accredited institution.    Valid medical license to practice.    Board certification in a relevant specialty, such as Internal Medicine.    Residency training in their specialty.    Strong clinical, diagnostic, and analytical skills.    Excellent communication and interpersonal skills.

As a healthcare IT professional, you will be responsible for leading the end-to-end implementation of Hospital Management and Information System (HMIS) solutions for clients in Mumbai and other focused cities. Your key responsibilities will include: - Leading the implementation of HMIS solutions, including system configuration, customization, and integration with existing healthcare IT infrastructure. - Collaborating with clients to gather and analyze requirements, ensuring the HMIS meets their specific needs. - Developing and executing implementation plans, ensuring milestones are achieved on time and within scope. - Serving as the primary technical point of contact for HMIS implementation projects, providing expert guidance on system functionality and configuration options. - Troubleshooting technical issues and working closely with the technical support team to resolve challenges promptly. - Building and maintaining strong relationships with internal and external stakeholders, ensuring their needs and expectations are understood and addressed. - Conducting user training sessions for clients and internal staff to ensure a smooth transition to the new HMIS. - Providing ongoing support to end-users, addressing inquiries, and resolving technical issues in a timely manner. - Developing and maintaining comprehensive documentation for end-users and internal teams. - Conducting thorough testing of HMIS configurations to ensure system reliability, accuracy, and compliance with industry standards. - Collaborating with the project management team to ensure successful project delivery. - Communicating effectively with clients to manage expectations, address concerns, and ensure satisfaction with HMIS implementations. - Collaborating with clients to assess system performance, identify opportunities for improvement, and implement enhancements. Qualifications required for this role include: - Bachelors degree in information technology, Computer Science, Healthcare Informatics, or a related field. Masters degree is a plus. - Proven experience (minimum of 5-7 years) in implementing and configuring healthcare information systems, with a focus on HMIS. Prior Consulting experience is preferred. - In-depth knowledge of HMIS solutions, Tele-medicine, healthcare data standards, and regulatory requirements. - Strong technical proficiency in relevant technologies, databases, programming languages, and cloud deployments. - Excellent communication and presentation skills, with the ability to convey technical information to non-technical stakeholders. - Demonstrated ability to manage multiple projects simultaneously and adapt to changing priorities. - Relevant certifications in healthcare informatics or related fields are highly desirable.,

Role Overview: As a Medical Science Liaison (MSL) at Alkem Laboratories Limited, you will play a crucial role in scientifically engaging, collaborating, and aligning with various external stakeholders to create value, address patient needs, and enhance the practice of medicine for improved patient access and outcomes. Your responsibilities will include leveraging scientific evidence during engagements, identifying impactful insights, contributing to product strategy, generating evidence plans, and collaborating with field matrix colleagues to support healthcare systems strengthening. Key Responsibilities: - Act as a strategic scientific partner by gathering insights for Patient Journey mapping, launch excellence roadmap, and integrated evidence generation plans - Serve as a Medical, Clinical, and Scientific expert on assigned therapeutic areas and Alkem Laboratories Ltd. compounds - Identify and map external stakeholders aligned with the medical strategy, and establish innovative partnership models for transforming clinical practice - Communicate relevant evidence to stakeholders in a timely manner to facilitate informed decision-making - Respond to unsolicited information requests from stakeholders regarding marketed and pipeline compounds - Manage administrative tasks efficiently, including customer relationship management, compliance training, and expense reporting - Travel nationally to engage with Key Opinion Leaders (KOLs) regularly, especially during new product launches - Play a key role in internal customer connections and contribute to equity and revenue building efforts - Promote and adhere to Ethics and Compliance Professional Practices Policy Qualifications Required: - Qualified Medical Professional with MBBS, BAMS, or BDS degree - Pharmacists, individuals with a Master's or post-graduate degree in health/life sciences are encouraged to apply; Doctoral degree (MPharm, PharmD, PhD) preferred,

Role Overview: You will be responsible for monitoring and managing all aspects of updating Reference Safety Documents such as CCDS, SmPC, PI, PIL, datasheets, and product monographs for all ADVANZ PHARMA products globally. You must ensure the maintenance of these documents in accordance with applicable guidelines. Your role will involve writing and managing global reference safety documents like CCDS and regional reference safety documents like SmPC for innovator drugs, branded drugs, generics, and biosimilars. Key Responsibilities: - Act as a subject matter expert in global labeling requirements, driving continuous improvement initiatives, and upholding high-quality standards. - Manage safety-related variations and maintain product information, ensuring effective communication with stakeholders. - Review and approve scientific documents such as SmPC and PIL for marketed products. - Provide scientific responses to Health Authorities related to the company's products and support submissions with appropriate data. - Coordinate and execute global labeling compliance activities across multiple regions to meet regulatory requirements. - Establish successful relationships with internal and external stakeholders. - Identify gaps in reference safety document management and lead remedial actions. - Participate in the preparation of drafts for SOPs and WIs to ensure consistency and accuracy. - Stay updated on changing PV requirements globally, focusing on Rest of World territories. - Collaborate with internal and external stakeholders to ensure Pharmacovigilance and Regulatory compliance. - Drive operational efficiencies across various teams and functions. - Maintain documentation as per Good Documentation Practices (GDP). Qualifications Required: - Post-graduate qualification in any discipline within Life sciences or Pharmacy. Additional Company Details: ADVANZ PHARMA is a global pharmaceutical company dedicated to improving patients" lives by providing specialty, hospital, and rare disease medicines. With a focus on being a partner of choice for commercializing medicines in Europe, Canada, and Australia, the company collaborates with biopharma and pharmaceutical development firms. Headquartered in London, UK, with a presence in over 20 countries, ADVANZ PHARMA's product portfolio includes innovative medicines, generics & biosimilars, and originator brands across various therapeutic areas. The company values entrepreneurship, speed, and integrity in achieving its ambition with the passion of its dedicated employees.,

**Job Description:** **Role Overview:** As an Intensivist/Jr. Intensivist at Surana Sethia Hospital And Research Centre in Mumbai, your primary responsibility will involve providing critical care to patients in the Intensive Care Unit (ICU). You will be in charge of managing life-support equipment, monitoring patients" condition, and working collaboratively with other medical professionals to ensure comprehensive patient care. Additionally, you will be expected to perform invasive procedures, interpret diagnostic tests, and actively participate in multi-disciplinary rounds. **Key Responsibilities:** - Provide critical care to patients in the Intensive Care Unit (ICU) - Manage life-support equipment and monitor patients" condition - Collaborate with other medical professionals for comprehensive patient care - Perform invasive procedures and interpret diagnostic tests - Participate actively in multi-disciplinary rounds **Qualifications Required:** - Strong skills in patient care, critical care management, and life support techniques - Proficiency in performing invasive procedures and interpreting diagnostic tests - Excellent communication and collaboration skills - Ability to work effectively in a high-pressure, fast-paced environment - MD/DNB/FCPS/DA/IDCCM/CTCCM-Internal Medicine, Emergency Medicine, or Anesthesia with Critical Care specialization - Valid medical license to practice in India - Experience in an Intensive Care Unit (ICU) setting is preferred,