581 Hematology Jobs - Page 11

Challenging. Meaningful. Life-changing. Those aren t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers. bms. com/working-with-us . Position: Senior Specialist, Biostatistics Location: Hyderabad At Bristol Myers Squibb, we are inspired by a single vision - transforming patients lives through science. In oncology, hematology, cell therapy, immunology and cardiovascular disease and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Position Summary The Senior Specialist, Biostatistics is a member of cross-functional study/project teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. These individuals develop collaborative relationships and work effectively with the Biostatistics Lead, and other cross functional team members. Key Responsibilities Contributes to designing clinical trials to address study hypotheses and objectives. Authors and/or reviews protocol synopsis, protocol, statistical analysis plan, data presentation plan, case-report forms, clinical study reports, associated publications, and other study level specification documents under supervision. Performs and/or validates preplanned or ad hoc statistical analyses with guidance as needed. Presents & interprets results to GBDS and/or cross-functional team members. Translates scientific questions into statistical terms and statistical concepts into layman terms. Compliant with BMS processes and SOPs, adherence to global and project standards within an indication or therapeutic area and responsible for quality of deliverable. Continually develops technical knowledge of statistical methodology and how it is appropriately applied in trial design and data analysis for clear, concise, high-quality results. Effectively communicates the GBDS Mission and Vision in a fashion that generates pride, excitement and commitment within GBDS. Enables a culture of inclusiveness, respect for diversity, compliance with process and allows for the questioning and challenging of others in a respectful and constructive manner. Qualifications & Experience Fresh MS in statistics, or biostatistics or related scientific field preferred. (0-2 years of experience) Proficiency in scientific computing/programming (SAS, R or Python) and implementation of statistical analysis, data manipulation, graphing & simulation. Good interpersonal, communication, writing and organizational skills Ability to: learn regulatory requirements & clinical trial design, data analysis and interpretation, work successfully within cross-functional teams, organize multiple work assignments and establish priorities Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. If you come across a role that intrigues you but doesn t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. With a single vision as inspiring as Transforming patients lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms. com . Visit careers. bms. com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers. bms. com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

We have Openings for Lab Technician in Trichy Call HR - 8310049303 Collecting blood samples: From patients or donors, either at a lab or through home collection. Maintaining the lab: Ensuring the lab is clean, organized, and equipped with necessary supplies and equipment. Conducting tests and analyzing samples: Using various laboratory equipment and techniques to test and analyze blood samples Work Location : Trichy Minimum 6months of Experience as Lab technician Immediate Joining Roles & Responsibilities : 1.Blood Collection 2.Lab Maintenance 3.Sample collection 4.Blood Sampling 5.Home collection

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . Position: Senior Specialist, Biostatistics Location: Hyderabad At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science. In oncology, hematology, cell therapy, immunology and cardiovascular disease and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Position Summary The Senior Specialist, Biostatistics is a member of cross-functional study/project teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. These individuals develop collaborative relationships and work effectively with the Biostatistics Lead, and other cross functional team members. Key Responsibilities Contributes to designing clinical trials to address study hypotheses and objectives. Authors and/or reviews protocol synopsis, protocol, statistical analysis plan, data presentation plan, case-report forms, clinical study reports, associated publications, and other study level specification documents under supervision. Performs and/or validates preplanned or ad hoc statistical analyses with guidance as needed. Presents & interprets results to GBDS and/or cross-functional team members. Translates scientific questions into statistical terms and statistical concepts into layman terms. Compliant with BMS processes and SOPs, adherence to global and project standards within an indication or therapeutic area and responsible for quality of deliverable. Continually develops technical knowledge of statistical methodology and how it is appropriately applied in trial design and data analysis for clear, concise, high-quality results. Effectively communicates the GBDS Mission and Vision in a fashion that generates pride, excitement and commitment within GBDS. Enables a culture of inclusiveness, respect for diversity, compliance with process and allows for the questioning and challenging of others in a respectful and constructive manner. Qualifications & Experience Fresh MS in statistics, or biostatistics or related scientific field preferred. (0-2 years of experience) Proficiency in scientific computing/programming (SAS, R or Python) and implementation of statistical analysis, data manipulation, graphing & simulation. Good interpersonal, communication, writing and organizational skills Ability to: learn regulatory requirements & clinical trial design, data analysis and interpretation, work successfully within cross-functional teams, organize multiple work assignments and establish priorities Why You Should Apply Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Job Title: Lab Technician – Hematology Location: Neuberg Diagnostics, Perungudi Shift: Rotational Gender Preference: Male candidate preferred Experience: Fresher to 1–2 years in Hematology Key Responsibilities: Conduct routine hematology investigations Operate lab instruments and maintain quality standards Handle samples and documentation accurately Follow safety and hygiene protocols Qualification: DMLT / BMLT Interested candidates can share their resume to: 6383907434 Job Type: Full-time Pay: ₹10,000.00 - ₹20,000.00 per month Benefits: Provident Fund Schedule: Morning shift Night shift Rotational shift Work Location: In person Application Deadline: 03/07/2025

Job Posting: Frontline Sales Executives (IVD Sales) – Delhi NCR Location: Delhi/NCR Positions: 4 Experience: 2-3 Years Industry: In-Vitro Diagnostics (IVD), Biochemistry, Hematology, CLIA We are hiring dynamic and driven Sales Executives to expand our footprint across Delhi NCR in the competitive IVD diagnostics space. Key Requirements: • Proven experience in direct field sales (no distributor/channel dependency) • Strong understanding of IVD kits, Biochemistry Analyzers, 3-part Hematology Analyzers, CLIA Systems • Must have successfully closed Reagent Rental deals • Domain knowledge and customer engagement skills • Science Graduate / BMLT / DMLT preferred • Own 2-wheeler with valid license for travel across NCR • Presentable appearance and excellent communication skills • Proficiency in MS Office, Email writing, and reporting tools • Comfortable working in a high-performance, target-driven environment • Capable of payment follow-ups and collections • Strong knowledge of competitor products and pricing • Candidates must be willing to travel extensively • Background verification will be conducted post shortlisting • Preference will be given to candidates with a proven sales track record • Attractive performance-based monthly incentives To apply, email your CV to contact@jitmcgenes.com , sarfraz.ahmad@jitmcgenes.com

Orange Health is an on-demand diagnostics service for Indian consumers that enables convenience, reliability and overall better healthcare outcomes. With our deep understanding of primary healthcare and its opportunities, we are building Orange Health to become the infrastructure of remote healthcare in India, starting with making diagnostics on-demand. Since our launch in 2020, Orange Health has grown fast to become a diagnostics leader in Bangalore by delivering a strong product experience. Our Founders: The founders Dhruv Gupta (Consumer tech entrepreneur with 2 successful exits) & Tarun Bhambra (Experienced corporate leader and VC investor) have 15+ years of combined healthcare experience and have together built a profitable health-tech business, serving 100m+ users. Our vision is supported by high-quality investors like Accel, General Catalyst, Y Combinator, along with marquee healthcare and global investors. Diagnostics is something that is going to meaningfully touch your family every day. Join us to make Diagnostics 10x more convenient, 10x more accurate - 10x better. Our Presence: We are currently serving Bangalore, NCR, Mumbai, Hyderabad, with a plan to enter other metro cities soon :) How will you make an impact? We are seeking a highly skilled and experienced Senior Lab Technician specializing in Biochemistry, Clinical Pathology, Serology and Hematology to join Orange Health in India. The ideal candidate should have significant experience and expertise in performing various tests using both manual and automated machines. As a Lab Technician, you will be responsible for conducting diagnostic tests, analyzing results, maintaining laboratory equipment, and ensuring the accuracy and quality of test outcomes. Why You Might Be Excited About Us We are on a mission to build the fastest diagnostic lab in India. We have a bunch of Talented folks who relentlessly work towards bringing a WOW customer experience. Rated currently at 4.9. Our team has a wide range of experience .Folks at OH have worked earlier with companies like flipkart,Practo, Unacademy, Swiggy, Metropolis, Licious, cure.fit etc. and we are excited to learn from you too. We care for your career & growth and hence we will help you to shape a career you are excited about. We work hard and we party harder. Our People NPS is >90% and Glassdoor rating is 4.9. Competitive Pay What will you get to do? Perform a wide range of diagnostic tests in the areas of Biochemistry, Clinical Pathology, and Hematology, using manual and automated machines. Prepare patient samples for analysis, ensuring proper labeling and adherence to standard operating procedures (SOPs). Operate and maintain automated laboratory instruments, troubleshoot any technical issues, and perform routine maintenance as required. Conduct calibration and quality control checks on laboratory equipment to ensure accurate and reliable test results. Analyze and interpret test results, record findings accurately, and prepare detailed reports for review by medical professionals. Adhere to safety protocols and maintain a clean and organized work environment to prevent cross-contamination and ensure a safe working environment. Collaborate with other laboratory staff and healthcare professionals to ensure efficient workflow and timely delivery of test results. Assist in the development and implementation of new testing methods and protocols, as required by the company. Keep abreast of the latest advancements in laboratory techniques, equipment, and relevant scientific research. Participate in continuing education programs and training sessions to maintain proficiency in laboratory practices. Adhere to company policies, guidelines, and ethical standards in all laboratory activities. Skills We Are Looking For Bachelor's degree in Biochemistry, Clinical Pathology, Hematology, or a related field. Proven experience of 6 - 10 years as a Senior Lab Technician in a diagnostic laboratory, with a focus on Biochemistry, Clinical Pathology, and Hematology. In-depth knowledge and hands-on experience with both manual and automated laboratory instruments used in diagnostic testing. Familiarity with laboratory safety protocols and quality control procedures. Strong analytical skills with the ability to interpret complex data and troubleshoot technical issues. Detail-oriented and organized approach to work, ensuring accuracy and precision in test results. Excellent communication skills, both written and verbal, to report findings and collaborate with team members effectively. Ability to work independently and as part of a team in a fast-paced and dynamic environment. Flexibility to work various shifts, including weekends and holidays, as required by the company's operational needs. Prior experience in a diagnostic company or healthcare setting will be an advantage. Join our dynamic and dedicated team of professionals at Orange Health, where you can contribute to improving healthcare outcomes through accurate and reliable diagnostic testing. Get to know us even more :) Website: https://www.orangehealth.in/ LinkedIn: https://www.linkedin.com/company/orange-health/mycompany/ Instagram: https://www.instagram.com/orangehealth.in/ Twitter: https://twitter.com/OrangeHealth_ Glassdoor: https://rb.gy/k1gkoz So if you think you have that extra"orange"nary quality in you, we can't wait to welcome you onboard :) Skills: laboratory safety protocols,automated laboratory instruments,data analysis,communication skills,hematology,biochemistry,microbiology,molecular,technical troubleshooting,manual laboratory instruments,pathology,clinical pathology,serology,quality control procedures,healthcare setting,analytical skills

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more careers.bms.com/working-with-us . Position Senior Specialist, Biostatistics Location Hyderabad At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science. In oncology, hematology, cell therapy, immunology and cardiovascular disease and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Position Summary The Senior Specialist, Biostatistics is a member of cross-functional study/project teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. These individuals develop collaborative relationships and work effectively with the Biostatistics Lead, and other cross functional team members. Key Responsibilities Contributes to designing clinical trials to address study hypotheses and objectives. Authors and/or reviews protocol synopsis, protocol, statistical analysis plan, data presentation plan, case-report forms, clinical study reports, associated publications, and other study level specification documents under supervision. Performs and/or validates preplanned or ad hoc statistical analyses with guidance as needed. Presents & interprets results to GBDS and/or cross-functional team members. Translates scientific questions into statistical terms and statistical concepts into layman terms. Compliant with BMS processes and SOPs, adherence to global and project standards within an indication or therapeutic area and responsible for quality of deliverable. Continually develops technical knowledge of statistical methodology and how it is appropriately applied in trial design and data analysis for clear, concise, high-quality results. Effectively communicates the GBDS Mission and Vision in a fashion that generates pride, excitement and commitment within GBDS. Enables a culture of inclusiveness, respect for diversity, compliance with process and allows for the questioning and challenging of others in a respectful and constructive manner. Qualifications & Experience Fresh MS in statistics, or biostatistics or related scientific field preferred. (0-2 years of experience) Proficiency in scientific computing/programming (SAS, R or Python) and implementation of statistical analysis, data manipulation, graphing & simulation. Good interpersonal, communication, writing and organizational skills Ability to learn regulatory requirements & clinical trial design, data analysis and interpretation, work successfully within cross-functional teams, organize multiple work assignments and establish priorities Why You Should Apply Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https //careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

We are looking for a skilled professional to join our team as an Assistant - Sample Collection at Vijaya Diagnostic Centre. The ideal candidate will have experience in the healthcare industry, specifically in sample collection and phlebotomy. Roles and Responsibility Collect and process samples from patients with precision and accuracy. Ensure proper storage and handling of biological samples to maintain their integrity. Collaborate with medical staff to ensure smooth sample collection processes. Maintain accurate records of sample collection and processing activities. Implement quality control measures to ensure high standards of sample collection practices. Develop and implement effective strategies to improve sample collection efficiency. Job Requirements Minimum 2 years of experience in sample collection or phlebotomy. Strong knowledge of healthcare procedures and protocols related to sample collection. Excellent communication and interpersonal skills. Ability to work effectively in a fast-paced environment with attention to detail. Familiarity with laboratory information systems and software applications. Ability to maintain confidentiality and handle sensitive information with discretion. Additional Info The selected candidate will be offered a competitive salary package and benefits.

We are looking for a skilled Phlebotomist to join our team at Vijaya Diagnostic Centre. The ideal candidate will have 1-3 years of experience in the healthcare industry, responsible for collecting and processing samples from patients. Roles and Responsibility Collect and process patient samples with precision and accuracy. Maintain confidentiality and handle sensitive information with discretion. Operate medical equipment and instruments safely and efficiently. Collaborate with healthcare professionals to ensure smooth sample collection processes. Ensure compliance with laboratory protocols and procedures. Maintain accurate records of sample collection and processing. Job Requirements Minimum 1 year of experience in phlebotomy or a related field. Strong knowledge of medical terminology and sample handling procedures. Ability to work effectively in a fast-paced environment. Excellent communication and interpersonal skills. Familiarity with medical equipment and instruments. Ability to maintain confidentiality and handle sensitive information.

We are looking for a highly skilled and experienced Assistant to join our team at Vijaya Diagnostic Centre in the healthcare industry. The ideal candidate will have 7-10 years of experience in sample collection. Roles and Responsibility Assist in the development and implementation of new sample collection procedures. Collaborate with cross-functional teams to ensure seamless sample collection operations. Develop and maintain relationships with key stakeholders, including healthcare professionals and patients. Conduct quality control checks on samples collected to ensure accuracy and integrity. Provide excellent customer service to patients and their families regarding sample collection. Maintain accurate records of sample collection activities and results. Job Requirements Strong knowledge of healthcare industry standards and regulations related to sample collection. Excellent communication and interpersonal skills are required for effective collaboration with healthcare professionals and patients. Ability to work in a fast-paced environment with attention to detail and organizational skills. Strong problem-solving skills are needed to resolve issues related to sample collection. Familiarity with laboratory information systems and software applications used for sample collection management. Ability to maintain confidentiality and handle sensitive information with discretion.

R&D (Synthesis) -Agrochemical Industry-Saykha,Gujarat. Industry Engineering Engineering Design R&D Quality Qualification M.Sc Key Skills R&D Synthesis R&D R&D Chemist Research & Development Executive UPLC HPLC GC R & D Chemical Agro We are looking for a skilled professional with 4 to 10 years of experience in R&D synthesis to join our team. The ideal candidate will have a strong background in research and development, particularly in synthesis. Roles and Responsibility Develop and implement new methods for synthesizing complex molecules. Collaborate with cross-functional teams to design and optimize experiments. Conduct literature reviews to stay updated on the latest developments in R&D synthesis. Design and execute experiments to test hypotheses and validate results. Analyze data and interpret results to inform future experiments. Maintain accurate records of experiments, results, and procedures. Job Requirements Strong understanding of chemical principles and laboratory techniques. Experience with R&D software and equipment. Excellent problem-solving skills and attention to detail. Ability to work independently and as part of a team. Strong communication and interpersonal skills. Familiarity with safety protocols and regulations.

Industry Pharma R&D Biotech Qualification M.Sc Key Skills Green Field Projects UPLC R&D R&D Chemist R&D Synthesis Brownfield M.Sc Chemistry Pharma Research Chemist We are looking for a skilled R&D (Synthesis) Professional with 4 to 10 years of experience to join our team in the Employment Firms/Recruitment Services Firms industry. The ideal candidate will have a strong background in research and development, particularly in synthesis. Roles and Responsibility Develop and implement new methods for synthesizing complex molecules. Collaborate with cross-functional teams to design and optimize experiments. Conduct literature reviews and analyze data to identify trends and areas for improvement. Design and execute experiments to test hypotheses and validate results. Analyze and interpret data to draw meaningful conclusions. Stay up-to-date with industry developments and advancements in chemistry. Job Requirements Master's degree in Chemistry or related field. Minimum 4 years of experience in R&D, preferably in synthesis. Strong knowledge of chemical principles and laboratory techniques. Excellent analytical and problem-solving skills. Ability to work independently and as part of a team. Effective communication and interpersonal skills. Experience working with employment firms/recruitment services firms is preferred.

Rama Super Speciality Hospital is looking for Professor Biochemistry to join our dynamic team and embark on a rewarding career journeyProfessor is a full-time academic position in a college or university, responsible for teaching, conducting research, and serving on committees. They play a critical role in contributing to the intellectual life of their institution and in preparing the next generation of professionals and leaders.Responsibilities:Teach a range of courses in the department, at both the undergraduate and graduate levelsConduct original research in the field and publish findings in academic journals and at conferencesAdvise students and mentor junior faculty membersParticipate in department and university-wide committees, such as curriculum committees and search committeesPursue external funding opportunities to support research and teaching activitiesEngage in professional development activities to stay current in the field and enhance teaching skillsRequirements:A record of successful teaching and research, with a strong publication record in academic journalsAbility to teach a range of courses in the department, at both the undergraduate and graduate levelsStrong communication and interpersonal skills, with the ability to mentor students and junior faculty membersA commitment to continued professional development and growth

Rama Super Speciality Hospital is looking for Neurologist to join our dynamic team and embark on a rewarding career journey Diagnose and treat disorders affecting the nervous system, including conditions like epilepsy, Alzheimers, stroke, migraines, Parkinsons disease, and multiple sclerosis Perform and interpret diagnostic tests such as EEGs, MRIs, CT scans, and EMGs to evaluate neurological function Develop personalized treatment plans, prescribe medications, and recommend therapies or surgical interventions when necessary Monitor patient progress, manage chronic conditions, and adjust treatments based on clinical outcomes Educate patients and their families about neurological disorders, treatment options, and lifestyle adjustments Collaborate with a multidisciplinary team including neurosurgeons, physiotherapists, and psychologists to ensure comprehensive care Maintain detailed and accurate patient records and documentation in accordance with healthcare regulations

Rama Super Speciality Hospital is looking for Pathologist to join our dynamic team and embark on a rewarding career journey Conduct laboratory tests and analyze results to diagnose health conditions. Develop and implement laboratory protocols and procedures. Collaborate with healthcare providers to provide diagnostic support. Monitor and assess laboratory performance and identify areas for improvement. Ensure compliance with laboratory regulations and standards. Prepare and present laboratory reports to management. Maintain accurate records of laboratory tests and results.

Rama Super Speciality Hospital is looking for Pulmonologist to join our dynamic team and embark on a rewarding career journey Diagnose and treat respiratory system disorders including asthma, COPD, tuberculosis, pneumonia, lung cancer, and sleep apnea Conduct and interpret diagnostic tests such as chest X-rays, CT scans, pulmonary function tests, and bronchoscopy procedures Develop and manage individualized treatment plans, prescribing medications, oxygen therapy, or non-invasive ventilation as needed Monitor patient progress and adjust treatments based on response and ongoing symptoms Collaborate with other specialists such as cardiologists, intensivists, and thoracic surgeons to provide comprehensive care Educate patients on disease management, lifestyle modifications, and preventive care for respiratory health Maintain detailed and accurate medical records in accordance with clinical standards and regulatory requirements

We are looking for a highly skilled and experienced LAB Chemist to join our team at Capital Placement Services. The ideal candidate should have a BSC degree in Chemistry with 6-8 years of experience. Roles and Responsibility Conduct laboratory tests and analyze results to ensure compliance with industry standards. Develop and implement new methods and procedures for laboratory testing and analysis. Collaborate with cross-functional teams to achieve project goals. Maintain accurate records of test results and laboratory activities. Ensure the laboratory is properly maintained and calibrated. Provide technical support and guidance to junior staff members. Job Requirements Bachelor's degree in Chemistry (BSC) or equivalent. Minimum 6 years of experience in a laboratory setting, preferably in an employment firm or recruitment services firm. Possess strong knowledge of chemical principles and laboratory techniques. Demonstrate excellent analytical and problem-solving skills. Ability to work independently and collaboratively as part of a team. Exhibit strong communication and interpersonal skills.

DMLT / B.Sc in Medical Laboratory Technology preferred. Analyze lab data and interpret results; learn new procedures Maintains quality results by running standards and controls Monitoring quality control measures and protocols ELISA

Position Summary: The Drug Safety Physician will be responsible for the pharmacovigilance function, including medical review and oversight of processing for all types of safety events. The individual will provide clinical support of drug safety data management and interpretation and risk management activities for the company, including oversight of clinical trial Serious Adverse Event (SAE) processing and safety data analysis to support signal detection and risk/benefit profile evaluation. This individual will ensure timely, consistent, and accurate safety reporting in accordance with FDA, EMA, and ICH guidelines, applicable regulatory requirements, Good Clinical Practice (GCP) and standard operating procedures (SOPs). Responsibilities (including but not limited to): Manage all aspects of Drug Safety and Pharmacovigilance, including leadership of safety data review, signal detection, risk communication including safety information updates, and mitigation of potential risks Provide medical and drug safety expertise to enable decision-making based on ongoing risk-benefit assessment, clinical trial data interpretation, and medical review of individual case reports of SAEs Work with CRO Safety Physicians/Team and Dragonfly's Medical Directors, Clinical Scientists and other functions on safety monitoring, assessment and reporting activities (case and aggregate) Input on safety sections in cross-functional documents (eg, study protocols, study reports, IBs, ICFs) and on responses to safety-related questions from regulatory agency, IRBs and Ethics Committees Act as the point of contact accountable for setting up and running DSMBs or safety data review meetings Participate in routine safety cohort reviews for ongoing Phase 1 dose escalation studies Perform event coding review and clinical & safety database reconciliation for consistent coding Oversee and manage Drug Safety system(s) to ensure compliance with safety data management and reporting requirements in all relevant territories and optimized safety database ownership and access for safety monitoring, signal detection and reporting Ensure effective SOPs and strong safety vendor governance are in place Proactively recommend and plan for future development of Drug Safety and Pharmacovigilance to enable regulatory filings and commercialization, including acquiring QPPV support and the participation in creating Risk Management Plans and a Pharmacovigilance System Master File Ensure audit and inspection readiness of the function at all times Education and Skills Required: MD required, with a minimum of 7 years in Drug Safety related activities in pharma/biotech (title commensurate with experience) Clinical trial experience, including oncology drug safety with least 3 years being in early clinical development Experience authoring, reviewing, and providing input to drug-safety related regulatory reports Successful involvement in regulatory agency interactions or inspections Strong knowledge of FDA, EU, ICH and other global regulatory requirements for safety reporting and safety data and risk management Solid medical knowledge and familiarity with medical concepts and terminology used in hematology/oncology clinical trials and safety monitoring Proficiency with using standard computer applications (eg Microsoft Office, Windows) and safety databases Possesses a sense of urgency and an ability to anticipate and respond quickly to emerging information Excellent oral and written communication skills for effectively interfacing with vendors and internal stakeholders Fosters strong relationships and values collaboration to develop and execute on plans Ability to multi-task in a fast-paced environment Self-motivated, conscientious, and enthusiastic about curing human diseases Other Required: Experience with case processing in ARGUS Demonstrated ability to challenge existing practices to become more effective. Ability to effectively adapt to a variety of situations. Meet quality and performance standards. Strong influencing skills Excellent communication skills, both written and oral Work effectively as a team member and promotes collaboration. Demonstrate ownership, initiative and accountability. Supervisory experience Less than 20% travel. Competencies: Ability to deliver on commitments and understanding of service culture. Communicates effectively and efficiently on safety issues to internal and external stakeholders. Maintain consistency of safety assessments. Serve in cross-functional teams as Drug Safety expert. Monitor regulatory compliance of safety reporting throughout trial. Lead and contribute to process development and/or process improvements that support Drug Safety Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

Company Description HEMATO-ONCOLOGY CLINIC (AHMEDABAD) PRIVATE LIMITED is a hospital and healthcare services provider located near Samved Hospital on Commerce College Road, Navrangpura, Ahmedabad, Gujarat. The clinic is dedicated to delivering specialized and high-quality hematology and oncology care in a patient-centered environment. Role: Operations Manager Location: On-site | Navrangpura, Ahmedabad Employment Type: Full-Time Salary: ₹50,000 – ₹55,000 CTC Role Description We are seeking an experienced Operations Manager to lead and oversee the day-to-day administrative and operational functions of the clinic. The ideal candidate will ensure smooth workflow, coordinate with clinical and non-clinical teams, and uphold the highest standards of patient care and facility management. Key Responsibilities Oversee daily clinical and administrative operations to ensure efficient and patient-centric service delivery. Manage vendor relationships, procurement processes, contract negotiations, and service quality. Supervise facility maintenance, infrastructure, and housekeeping operations. Plan and schedule staff deployment across departments to optimize resource utilization. Ensure compliance with healthcare regulations, including NABH and NABL standards. Collaborate with medical and administrative teams to streamline operational workflows. Oversee inventory and supply chain management for medical and non-medical supplies. Monitor key performance indicators (KPIs) such as turnaround times and patient wait times. Lead emergency preparedness and crisis response management initiatives. Assist the finance team with budgeting, cost control, and expense monitoring. Requirements Minimum 6 years of experience in healthcare operations management. Proven expertise in vendor management , property/facility oversight , and staff scheduling . Strong understanding of healthcare compliance and accreditation standards (NABH/NABL). Excellent leadership, communication, and problem-solving skills. Job Types: Full-time, Permanent Pay: Up to ₹55,000.00 per month Benefits: Health insurance Leave encashment Life insurance Paid sick time Paid time off Provident Fund Schedule: Day shift Morning shift Supplemental Pay: Overtime pay Yearly bonus Ability to commute/relocate: Navrangpura, Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Do you have proven experience in vendor management, facility management, and staff scheduling? The salary for this role is ₹50,000 – ₹55,000 CTC. Are you comfortable with this? Experience: Operations management: 1 year (Required) Work Location: In person

Post:- Lab Technician Qualification- B.sc/M.Sc- Chemistry Experience:- 1-3 Years Job Location- Bahadurgarh(HR) No. of Vacancy:- 2 No Job Description:- Must have hands on experience on different type of analytical instruments like HPLC, GC, Titrator & Others, Maintaining Day to Day Testing Records & Must have working experience in Oil testing/Pharmaceutical Lab Receive, label and analyze samples, Design and execute laboratory testing according standard procedures, make observations and interpret findings, ,Organize and store all chemicals substances, fluids and compressed gases according to safety instructions, Record all data and results in specified forms (paper and electronic) with accuracy and responsibility Maintain equipment and assist in ordering laboratory supplies, Ensure that all safety guidelines are followed strictly at all times and maintain a clean and orderly environment ,Perform routine and non- routine tests and analyses using the appropriate technical equipment and instruments, Receive or collect, as well as process, samples Calculate test results, and log and report results using a computer/Manual calculations, Prepare and supervise experiments ,Perform quality control and calibrate equipment if necessary ,Maintain equipment in proper working order and maintain a clean work area ,Practice safe work habits, including complying with all safety, health, and environmental rules and regulations

Company Description HEMATO-ONCOLOGY CLINIC (AHMEDABAD) PRIVATE LIMITED is a hospital and healthcare services provider located near Samved Hospital on Commerce College Road, Navrangpura, Ahmedabad, Gujarat. The clinic is dedicated to delivering specialized and high-quality hematology and oncology care in a patient-centered environment. Role: Operations Manager Location: On-site | Navrangpura, Ahmedabad Employment Type: Full-Time Salary: ₹50,000 – ₹55,000 CTC Role Description We are seeking an experienced Operations Manager to lead and oversee the day-to-day administrative and operational functions of the clinic. The ideal candidate will ensure smooth workflow, coordinate with clinical and non-clinical teams, and uphold the highest standards of patient care and facility management. Key Responsibilities Oversee daily clinical and administrative operations to ensure efficient and patient-centric service delivery. Manage vendor relationships, procurement processes, contract negotiations, and service quality. Supervise facility maintenance, infrastructure, and housekeeping operations. Plan and schedule staff deployment across departments to optimize resource utilization. Ensure compliance with healthcare regulations, including NABH and NABL standards. Collaborate with medical and administrative teams to streamline operational workflows. Oversee inventory and supply chain management for medical and non-medical supplies. Monitor key performance indicators (KPIs) such as turnaround times and patient wait times. Lead emergency preparedness and crisis response management initiatives. Assist the finance team with budgeting, cost control, and expense monitoring. Requirements Minimum 6 years of experience in healthcare operations management. Proven expertise in vendor management , property/facility oversight , and staff scheduling . Strong understanding of healthcare compliance and accreditation standards (NABH/NABL). Excellent leadership, communication, and problem-solving skills. Job Types: Full-time, Permanent Pay: Up to ₹55,000.00 per month Benefits: Health insurance Leave encashment Life insurance Paid sick time Paid time off Provident Fund Schedule: Day shift Morning shift Supplemental Pay: Overtime pay Yearly bonus Ability to commute/relocate: Navrangpura, Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Do you have proven experience in vendor management, facility management, and staff scheduling? The salary for this role is ₹50,000 – ₹55,000 CTC. Are you comfortable with this? Experience: Operations management: 1 year (Required) Work Location: In person

Position Summary: The Drug Safety Physician will be responsible for the pharmacovigilance function, including medical review and oversight of processing for all types of safety events. The individual will provide clinical support of drug safety data management and interpretation and risk management activities for the company, including oversight of clinical trial Serious Adverse Event (SAE) processing and safety data analysis to support signal detection and risk/benefit profile evaluation. This individual will ensure timely, consistent, and accurate safety reporting in accordance with FDA, EMA, and ICH guidelines, applicable regulatory requirements, Good Clinical Practice (GCP) and standard operating procedures (SOPs). Responsibilities (including but not limited to): Manage all aspects of Drug Safety and Pharmacovigilance, including leadership of safety data review, signal detection, risk communication including safety information updates, and mitigation of potential risks Provide medical and drug safety expertise to enable decision-making based on ongoing risk-benefit assessment, clinical trial data interpretation, and medical review of individual case reports of SAEs Work with CRO Safety Physicians/Team and Dragonfly’s Medical Directors, Clinical Scientists and other functions on safety monitoring, assessment and reporting activities (case and aggregate) Input on safety sections in cross-functional documents (eg, study protocols, study reports, IBs, ICFs) and on responses to safety-related questions from regulatory agency, IRBs and Ethics Committees Act as the point of contact accountable for setting up and running DSMBs or safety data review meetings Participate in routine safety cohort reviews for ongoing Phase 1 dose escalation studies Perform event coding review and clinical & safety database reconciliation for consistent coding Oversee and manage Drug Safety system(s) to ensure compliance with safety data management and reporting requirements in all relevant territories and optimized safety database ownership and access for safety monitoring, signal detection and reporting Ensure effective SOPs and strong safety vendor governance are in place Proactively recommend and plan for future development of Drug Safety and Pharmacovigilance to enable regulatory filings and commercialization, including acquiring QPPV support and the participation in creating Risk Management Plans and a Pharmacovigilance System Master File Ensure audit and inspection readiness of the function at all times Education and Skills Required: MD required, with a minimum of 7 years in Drug Safety related activities in pharma/biotech (title commensurate with experience) Clinical trial experience, including oncology drug safety with least 3 years being in early clinical development Experience authoring, reviewing, and providing input to drug-safety related regulatory reports Successful involvement in regulatory agency interactions or inspections Strong knowledge of FDA, EU, ICH and other global regulatory requirements for safety reporting and safety data and risk management Solid medical knowledge and familiarity with medical concepts and terminology used in hematology/oncology clinical trials and safety monitoring Proficiency with using standard computer applications (eg Microsoft Office, Windows) and safety databases Possesses a sense of urgency and an ability to anticipate and respond quickly to emerging information Excellent oral and written communication skills for effectively interfacing with vendors and internal stakeholders Fosters strong relationships and values collaboration to develop and execute on plans Ability to multi-task in a fast-paced environment Self-motivated, conscientious, and enthusiastic about curing human diseases Other Required: Experience with case processing in ARGUS Demonstrated ability to challenge existing practices to become more effective. Ability to effectively adapt to a variety of situations. Meet quality and performance standards. Strong influencing skills Excellent communication skills, both written and oral Work effectively as a team member and promotes collaboration. Demonstrate ownership, initiative and accountability. Supervisory experience Less than 20% travel. Competencies: Ability to deliver on commitments and understanding of service culture. Communicates effectively and efficiently on safety issues to internal and external stakeholders. Maintain consistency of safety assessments. Serve in cross-functional teams as Drug Safety expert. Monitor regulatory compliance of safety reporting throughout trial. Lead and contribute to process development and/or process improvements that support Drug Safety Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

Bangalore Karnataka India Job Type: Regular Full-time Division: Precision for Medicine Business Unit: Clinical Solutions Requisition Number: 5781 Position Summary: The Drug Safety Physician will be responsible for the pharmacovigilance function, including medical review and oversight of processing for all types of safety events. The individual will provide clinical support of drug safety data management and interpretation and risk management activities for the company, including oversight of clinical trial Serious Adverse Event (SAE) processing and safety data analysis to support signal detection and risk/benefit profile evaluation. This individual will ensure timely, consistent, and accurate safety reporting in accordance with FDA, EMA, and ICH guidelines, applicable regulatory requirements, Good Clinical Practice (GCP) and standard operating procedures (SOPs). Responsibilities (including but not limited to): Manage all aspects of Drug Safety and Pharmacovigilance, including leadership of safety data review, signal detection, risk communication including safety information updates, and mitigation of potential risks Provide medical and drug safety expertise to enable decision-making based on ongoing risk-benefit assessment, clinical trial data interpretation, and medical review of individual case reports of SAEs Work with CRO Safety Physicians/Team and Dragonfly’s Medical Directors, Clinical Scientists and other functions on safety monitoring, assessment and reporting activities (case and aggregate) Input on safety sections in cross-functional documents (eg, study protocols, study reports, IBs, ICFs) and on responses to safety-related questions from regulatory agency, IRBs and Ethics Committees Act as the point of contact accountable for setting up and running DSMBs or safety data review meetings Participate in routine safety cohort reviews for ongoing Phase 1 dose escalation studies Perform event coding review and clinical & safety database reconciliation for consistent coding Oversee and manage Drug Safety system(s) to ensure compliance with safety data management and reporting requirements in all relevant territories and optimized safety database ownership and access for safety monitoring, signal detection and reporting Ensure effective SOPs and strong safety vendor governance are in place Proactively recommend and plan for future development of Drug Safety and Pharmacovigilance to enable regulatory filings and commercialization, including acquiring QPPV support and the participation in creating Risk Management Plans and a Pharmacovigilance System Master File Ensure audit and inspection readiness of the function at all times Education and Skills Required: MD required, with a minimum of 7 years in Drug Safety related activities in pharma/biotech (title commensurate with experience) Clinical trial experience, including oncology drug safety with least 3 years being in early clinical development Experience authoring, reviewing, and providing input to drug-safety related regulatory reports Successful involvement in regulatory agency interactions or inspections Strong knowledge of FDA, EU, ICH and other global regulatory requirements for safety reporting and safety data and risk management Solid medical knowledge and familiarity with medical concepts and terminology used in hematology/oncology clinical trials and safety monitoring Proficiency with using standard computer applications (eg Microsoft Office, Windows) and safety databases Possesses a sense of urgency and an ability to anticipate and respond quickly to emerging information Excellent oral and written communication skills for effectively interfacing with vendors and internal stakeholders Fosters strong relationships and values collaboration to develop and execute on plans Ability to multi-task in a fast-paced environment Self-motivated, conscientious, and enthusiastic about curing human diseases Other Required: Experience with case processing in ARGUS Demonstrated ability to challenge existing practices to become more effective. Ability to effectively adapt to a variety of situations. Meet quality and performance standards. Strong influencing skills Excellent communication skills, both written and oral Work effectively as a team member and promotes collaboration. Demonstrate ownership, initiative and accountability. Supervisory experience Less than 20% travel. Competencies: Ability to deliver on commitments and understanding of service culture. Communicates effectively and efficiently on safety issues to internal and external stakeholders. Maintain consistency of safety assessments. Serve in cross-functional teams as Drug Safety expert. Monitor regulatory compliance of safety reporting throughout trial. Lead and contribute to process development and/or process improvements that support Drug Safety It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process. Any data provided as a part of this application will be stored in accordance with our Privacy Policy. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2021 Precision Medicine Group, LLC. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.

Company Description At NGIVD, we’re reimagining the way disease diagnosis works. We aim to create a world where accurate, timely, and affordable testing is accessible. By harnessing the power of Made in India, we’re developing diagnostic solutions that cater to local needs most efficiently while delivering global quality. Our manufacturing facility adheres to ISO 9001, ISO 13485, and ISO 14001 quality standards. The focus on meeting the dynamic healthcare needs of India drives our work on infectious and lifestyle diseases to bridge the gap between advanced research and real-world patient care. Role Description This is a full-time remote role for a Senior Sales Executive. The Senior Sales Executive will be responsible for identifying new business opportunities, developing and maintaining client relationships, meeting sales targets, and providing excellent customer service. The role involves market research, crafting sales strategies, conducting presentations, negotiating contracts, and collaborating with the marketing and product teams to align sales initiatives with company goals. Qualifications Proven track record in sales and business development able to sell hematology cell counter, biochemistry semiautomated analyser, reagents, rapid cards in Kota zone. must be from kota area only able to achieve monthly quarterly and yearly targets Excellent communication, negotiation, and presentation skills Strong understanding of the healthcare and diagnostics industry Ability to work independently and remotely Bachelor's degree in Business, Marketing, or related field Proficiency in CRM software and sales analytics Experience in market research and crafting sales strategies Strong problem-solving skills and a customer-centric approach Willingness to travel for client meetings and industry events as required