1006 Physiology Jobs - Page 11

About Us We are the independent expert in assurance and risk management. Driven by our purpose, to safeguard life, property, and the environment, we empower our customers and their stakeholders with facts and reliable insights so that critical decisions can be made with confidence. As a trusted voice for many of the world’s most successful organizations, we use our knowledge to advance safety and performance, set industry benchmarks, and inspire and invent solutions to tackle global transformations. About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About The Role As part of our continued growth, we are looking to recruit technical and experienced In-Vitro Diagnostic Medical Device Assessors and Lead Auditors. The successful candidates will be responsible for planning and conducting audits / assessments against the manufacturing of medical devices, in accordance with ISO 13485, IVDR 2017/746 and MDSAP standards, enabling the delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards. Key Accountabilities: Assessor Conduct assessments (either desk-based or on client’s sites) in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer communication. Conduct Technical File reviews specific for products being authorized. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete specific projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification decisions within target timescales and in line with DNV policies and accreditation/approval requirements. Key Accountabilities: Auditor Responsible to carry out audits of the manufacturer's quality management system (QMS) and of its suppliers and/or subcontractors when appropriate and to draw up records and reports on the corresponding audits. Conduct surveillance audits including follow-up activities in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer relationships. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification recommendations within target timescales and in line with DNV policies and accreditation/approval requirements. Project manage auditing teams, as appropriate, to maximize efficiencies, enhance client satisfaction and ensure compliance with standards. What we offer Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. *Benefits may vary based on position, tenure/contract/grade level* DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity. About You Assessors and Auditors shall have a technical college degree in a relevant product or medical area, as described below. In-Vitro Diagnostic devices: Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology Education In addition to a relevant educational degree, candidates must have a minimum 4 years’ work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the design, manufacturing, testing or use of the device in which they are qualified to Audit or Assessment, and/or experience as an assessor or auditor in a notified body. Specifically: Auditor - Practical experience in the quality management system and specific production process/technologies for the IVD medical devices. Assessor - Practical experience in conducting and/or assessing performance evaluation data or related scientific aspects with in-vitro diagnostic medical devices in one or more of the following areas Microbiology, Immunology, Genetic testing/Cancer Biology and Molecular Biology. A PhD in a relevant area for in-vitro diagnostic medical devices can substitute 3 years of work experience provided it includes 2 years’ experience in design, manufacture or testing. In addition to the above, knowledge of the following would be preferred: An excellent working knowledge of medical device management systems, standards and medical device compliance/auditing techniques. Work experience in positions with significant QA Regulatory or management systems responsibility. Experience with Harmonized medical device standards for In-Vitro diagnostic medical devices. Experience with Risk Management EN ISO 14971. Medical device experience from auditing/work. Experience auditing against recognized standards. Experience of working under own initiative and in planning and prioritizing workloads. Should have a flair for technical writing, essential for exhaustive report writing.

About Us We are the independent expert in assurance and risk management. Driven by our purpose, to safeguard life, property, and the environment, we empower our customers and their stakeholders with facts and reliable insights so that critical decisions can be made with confidence. As a trusted voice for many of the world’s most successful organizations, we use our knowledge to advance safety and performance, set industry benchmarks, and inspire and invent solutions to tackle global transformations. About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About The Role DNV Product Assurance AS is one of the leading Notified Bodies for IVD medical devices. The unit is entitled to carry out tasks related to conformity assessment of IVD medical devices with Regulation (EU) 2017/746 In Vitro Medical Devices before such products are placed on the market. The role of Clinical Assessor is to assess performance data supporting safety and performance of IVD medical devices. Main Tasks In This Role Are Performing assessment and preparing reports of clinical performance aspects of legal manufacturers' technical documentation according to the requirements given in the Regulation (EU) 2017/746. Evaluation of the summary of safety and performance reports for high-risk IVD medical devices. Review and approval of performance evaluation report and other relevant performance documentation for accuracy and compliance with the requirements in the Regulation (EU) 2017/746. Education And Competencies Required Clinical Assessors shall have a technical college degree in a relevant product or medical area, as described below. Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology What we offer A competitive compensation and benefit package DNV training and qualification program A professional community in a prestigious technological company Possibilities to work with interesting and challenging projects Access to an extensive competence network Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share.DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity. About You Candidates must have a minimum 4 years’ work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the Assessment of Performance evaluation data, including Scientific Validity and Clinical Performance, or conducting performance evaluation studies for IVD devices. A PhD in a relevant area for IVD medical devices can substitute 3 years of work experience provided that it includes 2 years’ experience in Performance evaluation. Personal Qualities Analytical approach. Strong communication skills. Customer focus. Excellent reporting skills. Ability to work independently and efficiently. Ability to form recommendations on certification in complex cases.

About Us The Indian Centre for Climate & Societal Impacts Research (ICCSIR) is a non-profit, public-private partnership organisation based in Mandvi, Kutchh, Gujarat, India. Registered under Section-08 of the Indian Companies Act, 2013, ICCSIR focuses on an integrated, multidisciplinary approach to research in climate science and societal adaptation. Our goal is to promote socio-economic and political stability on a global scale in the 21st century through a deep understanding of climate evolution. Job Description Manager – Seaweed Operations will be responsible for the end-to-end management of all seaweed cultivation activities, growth monitoring, harvesting, and initial post-harvest processing. Responsibilities include managing cultivation processes, monitoring the growth and health of seaweed, ensuring sustainability practices, coordinating with researchers and field workers, and maintaining equipment. This role requires a hands-on leader with a deep understanding of marine biology, aquaculture principles, and practical experience in seaweed farming. The incumbent will ensure optimal growth, yield, and quality of seaweed while adhering to sustainable practices and operational efficiency. The role also involves analysing data, preparing reports, and staying up-to-date with industry trends and advancements. Responsibilities Seaweed Centre Management: Oversee the establishment and operation of Seaweed Centre facilities, including spore collection, sporophyte development, and seeding lines/substrates. Manage for optimal growth and health of juvenile seaweed. Ensure proper water quality parameters (temperature, salinity, nutrients, etc.) are maintained in the Seaweed Centre. Out planting & Farm Operations: Plan and execute seaweed out planting activities at designated farm sites. Manage the installation, maintenance, and repair of cultivation infrastructure (lines, buoys, anchors, nets, etc.). Conduct regular inspections of farm sites to assess seaweed growth, health, and detect potential issues (e.g., disease, fouling, predation). Growth & Health Monitoring: Implement robust monitoring programs to track seaweed growth rates, biomass, and overall health. Identify and address issues such as disease, pests, and environmental stressors. Maintain detailed records of cultivation parameters, growth data, and observations. Harvesting & Post-Harvest: Plan and supervise seaweed harvesting operations, ensuring efficient and sustainable collection. Oversee initial post-harvest handling, including cleaning, sorting, and preparation for further processing or transport. Implement best practices for maintaining seaweed quality post-harvest. Research & Development Support: Collaborate with R&D teams on trials for new species, cultivation techniques, and environmental adaptations. Provide practical insights and data from farm operations to inform research initiatives. Team Leadership & Management: Recruit, train, and supervise a team of cultivation technicians Foster a safe, productive, and collaborative working environment. Develop and implement training programs for staff on cultivation techniques and safety protocols. Safety & Compliance: Ensure strict adherence to all health, safety, and environmental regulations and company policies. Implement and maintain biosecurity protocols to prevent disease outbreaks. Manage equipment maintenance and ensure safe operation of all tools and machinery. Reporting & Documentation: Maintain accurate and detailed records of all cultivation activities, including planting schedules, harvest yields, environmental data, and operational costs. Generate regular reports on farm performance, challenges, and recommendations. Budget Management: Assist in the development and management of the cultivation budget, controlling costs while optimising production. Job Requirements Preference for 5+ years of experience in seaweed cultivation, aquaculture, or marine biology Minimum 3 years of proven experience in commercial seaweed cultivation, ideally in Ulva Lactuca. Strong understanding of seaweed life cycles, physiology, and environmental requirements. Practical experience with marine farming infrastructure and equipment. Ability to operate boats and other marine equipment (e.g., winches, pumps) safely. Knowledge in environmental science or sustainability practices Master’s in Marine Biology, Aquaculture, Oceanography, Fisheries Science, Biology, Botany, Environmental Science, or related field Ability to work independently and in a team environment Strong data analysis and report writing skills Excellent organisational and team management abilities Effective communication and coordination skills Prior experience in project management is a plus

About Us We are the independent expert in assurance and risk management. Driven by our purpose, to safeguard life, property, and the environment, we empower our customers and their stakeholders with facts and reliable insights so that critical decisions can be made with confidence. As a trusted voice for many of the world’s most successful organizations, we use our knowledge to advance safety and performance, set industry benchmarks, and inspire and invent solutions to tackle global transformations. About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About The Role As part of our continued growth, we are looking to recruit technical and experienced In-Vitro Diagnostic Medical Device Assessors and Lead Auditors. The successful candidates will be responsible for planning and conducting audits / assessments against the manufacturing of medical devices, in accordance with ISO 13485, IVDR 2017/746 and MDSAP standards, enabling the delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards. Key Accountabilities: Assessor Conduct assessments (either desk-based or on client’s sites) in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer communication. Conduct Technical File reviews specific for products being authorized. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete specific projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification decisions within target timescales and in line with DNV policies and accreditation/approval requirements. Key Accountabilities: Auditor Responsible to carry out audits of the manufacturer's quality management system (QMS) and of its suppliers and/or subcontractors when appropriate and to draw up records and reports on the corresponding audits. Conduct surveillance audits including follow-up activities in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer relationships. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification recommendations within target timescales and in line with DNV policies and accreditation/approval requirements. Project manage auditing teams, as appropriate, to maximize efficiencies, enhance client satisfaction and ensure compliance with standards. What we offer Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. *Benefits may vary based on position, tenure/contract/grade level* DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity. About You Assessors and Auditors shall have a technical college degree in a relevant product or medical area, as described below. In-Vitro Diagnostic devices: Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology Education In addition to a relevant educational degree, candidates must have a minimum 4 years’ work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the design, manufacturing, testing or use of the device in which they are qualified to Audit or Assessment, and/or experience as an assessor or auditor in a notified body. Specifically: Auditor - Practical experience in the quality management system and specific production process/technologies for the IVD medical devices. Assessor - Practical experience in conducting and/or assessing performance evaluation data or related scientific aspects with in-vitro diagnostic medical devices in one or more of the following areas Microbiology, Immunology, Genetic testing/Cancer Biology and Molecular Biology. A PhD in a relevant area for in-vitro diagnostic medical devices can substitute 3 years of work experience provided it includes 2 years’ experience in design, manufacture or testing. In addition to the above, knowledge of the following would be preferred: An excellent working knowledge of medical device management systems, standards and medical device compliance/auditing techniques. Work experience in positions with significant QA Regulatory or management systems responsibility. Experience with Harmonized medical device standards for In-Vitro diagnostic medical devices. Experience with Risk Management EN ISO 14971. Medical device experience from auditing/work. Experience auditing against recognized standards. Experience of working under own initiative and in planning and prioritizing workloads. Should have a flair for technical writing, essential for exhaustive report writing.

About Us We are the independent expert in assurance and risk management. Driven by our purpose, to safeguard life, property, and the environment, we empower our customers and their stakeholders with facts and reliable insights so that critical decisions can be made with confidence. As a trusted voice for many of the world’s most successful organizations, we use our knowledge to advance safety and performance, set industry benchmarks, and inspire and invent solutions to tackle global transformations. About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About The Role DNV Product Assurance AS is one of the leading Notified Bodies for IVD medical devices. The unit is entitled to carry out tasks related to conformity assessment of IVD medical devices with Regulation (EU) 2017/746 In Vitro Medical Devices before such products are placed on the market. The role of Clinical Assessor is to assess performance data supporting safety and performance of IVD medical devices. Main Tasks In This Role Are Performing assessment and preparing reports of clinical performance aspects of legal manufacturers' technical documentation according to the requirements given in the Regulation (EU) 2017/746. Evaluation of the summary of safety and performance reports for high-risk IVD medical devices. Review and approval of performance evaluation report and other relevant performance documentation for accuracy and compliance with the requirements in the Regulation (EU) 2017/746. Education And Competencies Required Clinical Assessors shall have a technical college degree in a relevant product or medical area, as described below. Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology What we offer A competitive compensation and benefit package DNV training and qualification program A professional community in a prestigious technological company Possibilities to work with interesting and challenging projects Access to an extensive competence network Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share.DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity. About You Candidates must have a minimum 4 years’ work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the Assessment of Performance evaluation data, including Scientific Validity and Clinical Performance, or conducting performance evaluation studies for IVD devices. A PhD in a relevant area for IVD medical devices can substitute 3 years of work experience provided that it includes 2 years’ experience in Performance evaluation. Personal Qualities Analytical approach. Strong communication skills. Customer focus. Excellent reporting skills. Ability to work independently and efficiently. Ability to form recommendations on certification in complex cases.

Anaesthesiologist Required Gadchiroli Maharashtra Salary 3 to 3.5 Lakhs + Accommodation + Food Sonipat Haryana For ICU IDCCM Preferred Salary 3 to 4 Lakhs Bharatpur Rajasthan Salary 3.5 Lakhs + Acco Gurgaon Haryana Salary 2 Lakhs + Share Required Candidate profile Goalpara, Assam Salary 4 Lakhs + Accommodation Neemrana, Rajasthan Salary 3.5 - 4 Lakhs + Accommodation Bhiwani Haryana Salary 2.5 to 3 Lakhs + Accommodation

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com Looking to jump-start your career? We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry. We are offering a global fast track career where you can grow along with Indegene’s high-speed growth. We are purpose-driven. We enable healthcare organizations be future ready and our customer obsession is our driving force . We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work. If this excites you, then apply below. Medical Reviewer You will be responsible for : PRINCIPAL RESPONSIBILITIES: Responsible for medical review of ICSRs for accuracy, medical relevance, and overall consistency of information captured in the safety database against all the applicable supporting documents as per the client requirement Evaluate adverse events (AE) report for seriousness, listedness and ensures that all medically relevant information from the source documents is included Assessment of reported AE and serious adverse events (SAE) providing company causality assessment utilizing clinical and global introspection methodologies aligned with global regulations. Reviews the case narrative, coding, product/Indication, labeling in accordance with the respective reference safety documents, causality and medical history for medical completeness, accuracy, and overall medical content. Provide medical sign off on the case. Perform line listing review of non-serious cases and evaluates the coding and labelling and confirm the events are evaluated correctly Perform unblinding activities as applicable Ensure appropriate follow-up questions/questionnaires are sent out based on the case. Perform Literature Surveillance when required Medical review of Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements Provide aggregate reviews of safety information, including but not limited to clinical data, post marketing, and literature review Tracking of inconsistencies on activities performed by data entry and QC reviewer as per the checklist and provide unbiased feedback, suggestions, points of improvement for attaining quality standards as per client expectations Responsible for following international pharmacovigilance regulations, company and department SOPs and department and function working practices. Contribute to pharmacovigilance and risk management planning for designated products by preparation of safety surveillance strategy and tracking and evaluating potential issues. Review safety assessments, risk/benefits evaluations, provide inputs and value add from medical perspective at all stages of safety Review, author and update standard operating procedures (SOP) and support in global initiatives for ensuring enhanced quality and compliance Communicate the observations to the applicable stakeholders and ensure the appropriate root cause analysis (RCA)/corrective action and preventive action (CAPA) Ensures follow up information is requested on relevant reports Present QA data to the responsible internal stakeholders in an appropriate forum as required Attend all the internal trainings and client trainings and ensure compliance with applicable guidelines Attend all the Governance and team meetings as required and appropriate Qualification : MBBS is required ( MCI registration is mandatory ) Your impact: About you: Must have: Cognitive abilities including verbal reasoning, attention to detail, critical thinking, scientific accuracy, and analytical ability. Ability to understand the purpose and requirements of a project. Good comprehension skills. Good communication and interpersonal skills. Drive quality and ensure team meets deadlines and commitments. Excellent mentoring and training skills. Knowledge of disease pathology and physiology, pharmacology and therapeutics. Familiarity with pharmaceutical industry principles of drug development and pharmacovigilance is preferred but not required. Very good understanding and track record in pharmacovigilance that can be applied and executed. Sound knowledge in pharmacovigilance safety database and compliance activities. EQUAL OPPORTUNITY Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

We require doctors for Medical Colleges & Hospitals PAN India Qual: MD/MS, DNB, (All Dept) Position: Consultant, SR, AP, Associate Professor, Professor Department: Clinical & Non Clinical Vishakha Call/Whatsapp: 9041008939 weps.services17@gmail.com

Hiring SR/AP Professor Ophthalmology Pediatrician General Medicine Surgeon Orthopedic Gynecology Emergency Medicine Anesthesia Community medicine Radiology Pharmacology Forensic Biochemistry Physiology for Medical College in Jaipur & Udaipur

1. Academic Qualifications: MBBS degree from a recognized university/institution. MD (Physiology) from an NMC-recognized medical college. Key Responsibilities of Assistant Professor in Physiology A. Teaching & Academic Duties Teach MBBSstudents Conduct: Lectures , small group discussions , and practical sessions Demonstrations using lab equipment, charts, and digital simulation tools Assist in internal assessments, paper setting, and viva exams. B. Laboratory & Practical Responsibilities Supervise clinical physiology experiments such as: Blood pressure measurement Spirometry ECG interpretation Reflex testing Ensure proper functioning and calibration of lab equipment. Help students learn lab techniques, safety protocols, and analysis. C. Research Involvement Participate in departmental research initiatives or interdisciplinary projects. Assist senior faculty in: Research data collection and analysis Preparing abstracts and manuscripts for publication Present work in conferences or CME events. D. Departmental & Administrative Support Contribute to: Timetable preparation Maintaining teaching records , logbooks, and academic documentation Organizing seminars, journal clubs, student quiz sessions Help with NMC inspection documentation and departmental presentations.

Greetings from Shiash Info Solutions! We are looking for experienced ED Fac/Profee Coders to join our team in Chennai. The ideal candidate should have a minimum of 2 years of experience in this field and be certified. Immediate joiners are preferable for this full-time on-site role. As an ED Coder at Shiash Info Solutions, your primary responsibility will be to handle day-to-day coding tasks associated with emergency department medical records. You will play a crucial role in ensuring accurate coding practices that comply with regulations and coding guidelines. To excel in this role, you should demonstrate proficiency in medical coding and classification systems such as ICD-10-CM and CPT. A strong knowledge of medical terminology, anatomy, and physiology is essential. Understanding healthcare regulations and compliance requirements is crucial for this position. Attention to detail and accuracy in coding practices are key attributes we are looking for. Additionally, effective communication skills and the ability to collaborate within a team environment are important. If you meet the qualifications and are interested in this opportunity, please share your resume with us at shiash.amaldia@gmail.com. For further inquiries, you can reach out to us at 6379869508. We look forward to receiving your application and potentially welcoming you to our team at Shiash Info Solutions in Chennai!,

Genpact (NYSE: G) is a global professional services and solutions firm delivering outcomes that shape the future. Our 125,000+ people across 30+ countries are driven by our innate curiosity, entrepreneurial agility, and desire to create lasting value for clients. Powered by our purpose the relentless pursuit of a world that works better for people we serve and transform leading enterprises, including the Fortune Global 500, with our deep business and industry knowledge, digital operations services, and expertise in data, technology, and AI. Inviting applications for the role of Business Analyst, Medical Coding In this role, you need to work as Medical coder for Provider Coding. Responsibilities Review medical records, patient medical history and physical exams, physician orders, progress notes, consultation reports, diagnostic reports, operative and pathology reports, and discharge summaries to verify the pertinent CPT and ICD 10 CM codes. To code on Medical reports by assigning appropriate CPT & ICD 10 CM codes based on the documentation and per the client specification. Follow project-specific guidelines without any deviation. Check the LCD policy per insurance specification. Performs assigned tasks/complete targets with speed and accuracy as per client SLAs Compliance with client/project guidelines, business rules, and training provided the company's quality system and policies. Communication / Issue escalation to supervisor if there is any in a timely manner. Willing to learn and keep self-updated with the updated codes. Work cohesively in a team setting. Assist team members to achieve shared goals. Qualifications we seek in you! Minimum Qualifications Must have relevant experience in Medical Coding any (ED, E/M, Urgent Care, Ancillary (Path/Lab/Rad) Thorough knowledge of CPT and ICD-10-CM/PCS, HCPCS Level II, Medicare, Medicaid, and Insurance guidelines. Coding certification: Mandatory CPC (AAPC) and/or CCS (AHIMA) Science graduate/BAMS/BHMS/BPT/BUMS and/or relevant equivalent and relevant work experience Preferred Qualifications/ Skills Relevant years general medical coding experience. Must possess computer skills including, but not limited to, Word, Excel, and PowerPoint. Experience with 3M and encoder preferred. Experience with an EPIC preferred. Must be able to use the internet and other electronic resources for the purpose of research. Advanced understanding of Professional coding guidelines, medical terminology, pharmacology, body systems/anatomy, physiology, and concepts of disease processes Job Business Analyst Primary Location India-Gurugram Schedule Full-time Education Level Bachelor's / Graduation / Equivalent Job Posting Apr 1, 2025, 8:46:35 PM Unposting Date Ongoing Master Skills List Operations Job Category Full Time,

Assign codes to diagnoses and procedures, using ICD and CPT codes - Ensure codes are accurate and sequenced correctly in accordance with Government and Insurance regulations - Follow up with the provider on any documentation that is insufficient or unclear - Communicate with other clinical staff regarding documentation - Search for information in cases where the coding is complex or unusual - Receive and review patient charts and documents for accuracy - Review the previous day's batch of patient notes for evaluation and coding - Ensure that all codes are current and active Skills/Experience : - Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Nursing - Strong knowledge of Anatomy, Physiology and, Medical terminology - 2-4 Years- experience in Medical Coding - Certification is preferred - Fluent verbal communication abilities - Knowledge of Healthcare terminology and ICD/CPT codes - Strong reporting skills - Familiar with Microsoft Excel - Excellent typing and accuracy

Designation : Medical Coder Full Time Opportunity Location : Multiple Job Description : Assign codes to diagnoses and procedures, using ICD and CPT codes - Ensure codes are accurate and sequenced correctly in accordance with Government and Insurance regulations - Follow up with the provider on any documentation that is insufficient or unclear - Communicate with other clinical staff regarding documentation - Search for information in cases where the coding is complex or unusual - Receive and review patient charts and documents for accuracy - Review the previous day's batch of patient notes for evaluation and coding - Ensure that all codes are current and active Skills/Experience : - Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Nursing - Strong knowledge of Anatomy, Physiology and, Medical terminology - 2-4 Years- experience in Medical Coding - Certification is preferred - Fluent verbal communication abilities - Knowledge of Healthcare terminology and ICD/CPT codes - Strong reporting skills - Familiar with Microsoft Excel - Excellent typing and accuracy

Designation : Medical Coder Full Time Opportunity Location : Multiple Job Description : Assign codes to diagnoses and procedures, using ICD and CPT codes - Ensure codes are accurate and sequenced correctly in accordance with Government and Insurance regulations - Follow up with the provider on any documentation that is insufficient or unclear - Communicate with other clinical staff regarding documentation - Search for information in cases where the coding is complex or unusual - Receive and review patient charts and documents for accuracy - Review the previous day's batch of patient notes for evaluation and coding - Ensure that all codes are current and active Skills/Experience : - Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Nursing - Strong knowledge of Anatomy, Physiology and, Medical terminology - 2-4 Years- experience in Medical Coding - Certification is preferred - Fluent verbal communication abilities - Knowledge of Healthcare terminology and ICD/CPT codes - Strong reporting skills - Familiar with Microsoft Excel - Excellent typing and accuracy

Assign codes to diagnoses and procedures, using ICD and CPT codes - Ensure codes are accurate and sequenced correctly in accordance with Government and Insurance regulations - Follow up with the provider on any documentation that is insufficient or unclear - Communicate with other clinical staff regarding documentation - Search for information in cases where the coding is complex or unusual - Receive and review patient charts and documents for accuracy - Review the previous day's batch of patient notes for evaluation and coding - Ensure that all codes are current and active Skills/Experience : - Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Nursing - Strong knowledge of Anatomy, Physiology and, Medical terminology - 2-4 Years- experience in Medical Coding - Certification is preferred - Fluent verbal communication abilities - Knowledge of Healthcare terminology and ICD/CPT codes - Strong reporting skills - Familiar with Microsoft Excel - Excellent typing and accuracy

Position Responsibilities – Thorough understanding of the contents of medical record in order to identify information to support coding. Basic knowledge of anatomy & physiology of human body and diseases in order to understand etiology, pathology, symptoms, signs, diagnostic studies, treatment modalities, and procedures to be coded. Basic understanding of claims form and reimbursement process. Abstracts pertinent information from patient medical records. Assigns ICD-10-CM, CPT/HCPCS codes, and modifiers. Utilizing CCI edits, LCD policies, CPT and Clinical guidelines while assigning codes. Reviews denials for coding lapses and suggests coding changes for corrective and preventive (root cause) action by DHT (denial handling team) team. Actively reviews denials and research to create claims scrubber edit which will prevent specific coding denials permanently. Notifies Coding Manager/Account Manager or designated individual when reports are incomplete, and code assignments are not straightforward or documentation is inadequate and updates relevant logs. Keeps self-updated of coding guidelines and federal reimbursement requirements, actively participates in and contributes to coding team presentations on Advance/Refresher Coding topics Abides by Standards of ethical coding as set forth by American Academy of Professional Coders (AAPC) and American Health Information Management Association (AHIMA) and adheres to official coding guidelines. Position Qualifications – Must be a graduate, preferably in Life Science, with basic training in medical transcription or medical coding, or coding certificate program with AAPC/AHIMA certification status (CIRCC/CPC/COC)/CCS) preferred. Must be ICD-10 certified.

Renai Medicity is looking for Senior Neuro Surgeon to join our dynamic team and embark on a rewarding career journeySpecializes in the surgical treatment of conditions affecting the brain, spinal cord, and nervesResponsibilities include evaluating patients, ordering and interpreting diagnostic tests, developing treatment plans, and performing surgeries.Prescribing medication and performing follow-up evaluations.Must have strong surgical skills, as well as a thorough understanding of anatomy, physiology, and medical technologies.

Renai Medicity is looking for Trauma Surgeon to join our dynamic team and embark on a rewarding career journeyA surgeon is a medical doctor who specializes in performing surgical procedures to treat injuries, diseases, and deformities through operative techniques. Surgeons undergo extensive training, typically completing medical school followed by a residency program focused on surgery. They possess advanced knowledge of human anatomy, physiology, and medical technology. Surgeons work in various specialties such as general surgery, orthopedic surgery, neurosurgery, cardiovascular surgery, and more. Their responsibilities include diagnosing patients, planning and performing surgical procedures, collaborating with other medical professionals, and providing post-operative care. Surgeons require excellent technical skills, decision-making abilities, and communication skills to effectively manage complex medical conditions and ensure the best possible outcomes for their patients.

Greetings from QI SPINE CLINIC !!! Overview We are seeking a dedicated and skilled Physiotherapist to join our healthcare team. The ideal candidate will be passionate about patient care and possess a strong understanding of medical terminology, physiology, and anatomy. This role involves working with patients of various ages, including paediatrics, to assess their physical conditions and develop tailored treatment plans aimed at improving mobility and quality of life. Responsibilities Conduct thorough assessments of patients' physical conditions and needs. Develop individualised treatment plans based on assessment findings. Implement therapeutic exercises and interventions to enhance patient recovery. Educate patients and their families on injury prevention and rehabilitation techniques. Maintain accurate patient records and documentation in compliance with hospital protocols. Collaborate with multidisciplinary teams to ensure comprehensive patient care. Stay updated with advancements in physiotherapy practices and medical knowledge. Requirements A recognised degree in Physiotherapy or equivalent qualification. Strong knowledge of medical terminology, physiology, and anatomy. Experience in paediatrics is advantageous but not mandatory. Excellent communication skills to effectively interact with patients and healthcare professionals. Ability to demonstrate empathy and provide high-quality patient care. Previous experience working in a hospital setting is preferred but not essential. A commitment to continuous professional development and learning. We invite qualified candidates who are eager to make a difference in the lives of others through effective physiotherapy practices to apply for this rewarding opportunity. Job opening- for CONSULTING PHYSIOTHERAPIST with us India's first chain of clinics dedicated to Spine Rehabilitation with German Technology. Location : Bangalore: Malleshwaram, Indira Nagar, Jayanagar SHIFT TIMINGS: Any 8 hrs Shift between 7am to 9pm Any 6 days working / 1 day week off SALARY – up to 4.5 LPA for MPT, & up to 3.5 LPA for BPT (depending on Clinical Knowledge & experience) 10% TDS applicable which is 100% recoverable when filing ITR TRAINING will be given on MTD Techniques, Mckenzie, Maitland, Mulligan, Neuro dynamics Kinetic Controls, etc. RESPONSIBILITIES AND DUTIES: Diagnosing and treating patients with musculoskeletal problems Recommending the services and products to the patients for their treatment. 1.5 YEARS BOND IS APPLICABLEQUALIFICATIONS AND SKILLS 1) Must have 0 - 1 year of experience in practicing physiotherapy and treating patients with musculoskeletal problems 2) Fresher are most welcome. 3) Bachelors in Physiotherapy (completed 6 months internship) or Masters in physiotherapy 4) Fluency in English is a must There will be 2 rounds of Interview- 1) CLINICAL 2) MANAGEMENT Kindly share your CV on 7304649270 Regards, Rosanne Talent Acquisition Team

Applications are invited for the post of Senior Resident in the following disciplines: Anatomy, Physiology, Biochemistry, Pharmacology & Microbiology Eligibility for Senior Resident: 1. Postgraduate degree in the subject Doctor of Medicine (MD) or Diplomate of National Board (DNB) in the subject. 2. Postgraduate Medical degree in Master of Science (MSc) with Doctor of Philosophy (PhD) shall be eligible for appointment as a Senior Resident. For further information kindly contact at 82889-69200 Mail your CV at principal@dmch.edu by 25th July 2025

About the Role We are looking for a highly skilled Biology Subject Matter Expert (SME) to develop high-quality content for NEET preparation . The ideal candidate should have in-depth knowledge of Botany and Zoology , a strong understanding of conceptual clarity , and a passion for developing high-quality, error-free content for students. Key Responsibilities Develop error-free and conceptually strong content for NEET Biology . Create questions, solutions, and explanations aligned with the latest NEET syllabus and exam pattern . Design full-syllabus tests, practice sheets, and concept notes to enhance students’ problem-solving skills. Review and improve existing content to maintain high accuracy and clarity . Work closely with the DTP and faculty team to ensure high-quality content presentation. Develop video solutions/hardcopy solutions for digital content, if required. Qualifications & Skills Bachelor's or Master’s degree in Biology, Life Sciences, or a related domain . Freshers & experienced candidates who have a strong understanding of the NEET syllabus, difficulty level, and exam trends are welcome to apply. Strong expertise in Human Physiology, Plant Physiology, Genetics, Ecology, and other core NEET Biology topics . Note: This is a content expert position , not a teaching role. If you are looking to grow as an educator , please do not apply Job Type: Full-time Pay: ₹18,000.00 - ₹25,000.00 per month Benefits: Food provided Provident Fund Schedule: Morning shift Work Location: In person

Job Responsibilities 1. To analyse and prepare working plan for the territory basis the data provides/ market research 2. To be able to follow up, monitor and achieve targets of the territory 3. Implementation & execution of all strategies 4. Stakeholder engagement- doctors, stockist, retailers, chemists and institutions pharmacy 5. Discipline and punctual with set timelines for multiple internal processes 7. Basic computer skills- excel working, word & email exchanges 6. Fast learner and adaptable to change in market 7. Strong communication skills (verbal)- English and local language 8. Effective in-clinic performance 9. Basic understanding and ability to explain anatomy physiology and product portfoli0 10. Organizing Camps (CME) as per the division strategy and customer needs 11. Prescription audit for Abbott brands and other competitors' brands 12. Generate POBs for Abbott brands as per the business plan Experience 2+ years of experience Fresher with good communication skills and analytical skills may also consider Required Qualification B.Sc. / B.Pharma. Preferred Candidate Candidate with prior / current experience in same therapy. Candidate from MNC and Top Indian pharma companies will have added advantage

About Us: We are an early-stage MedTech startup on a mission to design and develop accurate, affordable, and accessible medical equipment for India and the global market. Our work sits at the intersection of biomedical innovation, user-centric design, and social impact. We are building a platform to reimagine healthcare delivery, especially in under-served markets. As the core team member, you will play a pivotal role in shaping the technical foundation, culture, and direction of our company. You will get an opportunity to build & lead a team from scratch. Key Responsibilities: • Lead end-to-end design and development of innovative medical devices from concept to prototype and production. Build required team. • Translate clinical needs and healthcare challenges into technical specifications and product architecture. • Oversee design validation, risk analysis, and regulatory compliance (IEC 60601, ISO 13485, etc.). • Collaborate with external consultants, design partners, hospitals, and manufacturing teams. • Manage and mentor junior engineers as the team grows. • Participate in grant proposals, product strategy, and roadmap discussions with the founders. • Support regulatory submissions (CDSCO, FDA, CE) and quality system setup. • Stay updated on emerging biomedical technologies and trends. Required Qualifications & Skills: • M.Tech / M.E. in Biomedical Engineering or related field (preferred); exceptional candidates with B.Tech + significant experience will also be considered. • 5–7 years of hands-on experience in design & development of medical devices (preferably Class I or II). • Strong foundation in biomedical instrumentation, electronics, sensors, or mechanical aspects of device design. • Experience in CAD tools (SolidWorks, Creo), circuit design, embedded systems, or signal processing (as per specialization). • Exposure to product lifecycle management, prototyping, testing, and DFM (Design for Manufacturing). • Familiarity with clinical workflows, anatomy/physiology, and user-centric healthcare design. • Understanding of regulatory frameworks, standards, and risk management. Preferred Attributes: • Startup mindset: hands-on, self-driven, curious, and outcome-oriented. • Strong problem-solving and systems thinking abilities. • Ability to work independently in an unstructured, early-stage environment. • Passion for improving healthcare access and quality through innovation. • Strong communication and collaboration skills. What We Offer: • Founding team role with equity/ESOP potential. • Opportunity to shape next-generation MedTech solutions with real-world impact. • Exposure to leading hospitals, research institutes, and design collaborators. • A culture of innovation, purpose, and long-term vision.

⛔ This position is no longer available. University: McGill University Country: Canada Deadline: June 15, 2025 The Department of Kinesiology and Physical Education (KPE) at McGill University invites applications for the SASSI Postdoctoral Fellowship in sport science. This position is designed for recent or soon-to-be PhD graduates seeking to advance research in human sport performance within a dynamic academic environment. The fellowship aims to support research projects that enhance the understanding, facilitation, and optimization of sport performance, with a preference for endurance sport science. Foundational research with indirect ties to sport may also be considered if the impact on sport science research is clearly described. Requirements – PhD (recent or near completion) in Kinesiology, Exercise Science, Physiology, Human Performance, Sports Medicine, or a related field – Demonstrated research experience relevant to sport science – Strong communication and collaboration skills Fellowship Details – Duration: 2 years – Salary: $50,000 annually (includes benefits; unionized position) – One position available Application Deadline: June 15, 2025 Apply online: https://lnkd.in/e4y_JnPp Interested candidates are encouraged to apply and to share this opportunity with peers or colleagues who may be interested. The position will also be posted on the SASSI website and shared with incoming and current graduate students. Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/register Also See Fully Funded PhD Position in High-Performance Swimming Research Ph.D. Opportunities in Neuromechanics and Artificial Intelligence for Human Movement Research PhD or MSc Position in Permafrost Carbon Cycling PhD Program in Analytics for Economics and Management (AEM) Postdoctoral and PhD Opportunities in Exoskeleton Control, Mechatronic Design, and Biomechanics