Laboratory Technician Mission: The mission of the position Laboratory Technician is to drive sustainable growth and foster strategic partnerships, through innovative approaches, relentless pursuit of new opportunities, and a commitment to customer success, our Laboratory Technician play a pivotal role in positioning our organization as a market leader. Guided by integrity, collaboration, and a passion for excellence, we strive to create lasting value for our customers, stakeholders, and the company as a whole. Job Responsibilities: 1. Sample Handling and Processing: Specimen Collection and Preparation: Collect, label, and prepare patient samples with utmost accuracy and adherence to protocols. Ensure proper handling and storage of specimens to maintain sample integrity. Laboratory Testing: Conduct a variety of diagnostic tests following established procedures and safety protocols. Operate laboratory equipment such as analyzers, microscopes, and centrifuges proficiently. Perform quality control checks to ensure accuracy and precision of test results. 2. Analysis and Reporting: Data Analysis: Analyze test results meticulously, recording and interpreting findings accurately. Document and maintain comprehensive records of all tests conducted and results obtained. Report findings promptly to supervisory personnel for further review or action. 3. Equipment Maintenance and Calibration: Instrument Maintenance: Perform routine maintenance on laboratory equipment to ensure proper functioning. Calibrate and troubleshoot equipment issues promptly or report them to the appropriate personnel. Maintain inventory of reagents, supplies, and equipment, ensuring adequate stock levels. 4. Quality Assurance and Compliance: Quality Control: Adhere strictly to quality control and quality assurance procedures, following regulatory guidelines. Participate in proficiency testing programs to validate laboratory procedures and maintain accuracy. Assist in the implementation of quality improvement initiatives to enhance laboratory operations. 5. Safety and Hygiene: Safety Protocols: Maintain a clean and sterile laboratory environment, following safety protocols at all times. Dispose of bio hazardous materials and waste in accordance with established procedures. Adhere to infection control measures and ensure compliance with safety regulations. *This job description provides a general outline of responsibilities and qualifications and is not exhaustive. The role may be required to perform additional duties as necessary for the smooth functioning of the business. Qualification A diploma or associate degree in Medical Laboratory Technology, Clinical Laboratory Science, or a related field. Previous experience (1-2 years) in a laboratory setting, especially in diagnostic or clinical laboratories, is advantageous. Proficiency in conducting various laboratory tests and operating laboratory equipment. Knowledge of laboratory procedures, protocols, and safety measures. Ability to perform quality control checks and maintain accurate records of tests conducted. Strong analytical and problem-solving skills to interpret test results accurately. Attention to detail and precision in handling and processing specimens. Capability to manage multiple tasks efficiently in a fast-paced laboratory setting. Flexibility to adapt to changing priorities and work schedules. Good communication skills to interact effectively with colleagues and superiors. Ability to work collaboratively in a team-oriented environment.

Qualification : DNB-Radiology / MD-Radio Diagnosis. Contact Details Kanika Malhotra 9592419648

Job Role: Staff Nurse Location: Bareilly Qualification: GNM/ B.Sc. Nursing Years of Experience: 1- 5 years exp Interested candidate can share updated resume on sheetal.devadiga@indiraivf.in.

Post- Lady Medical Officer (MBBS) Location- DADRI, Greater Noida. Project- NTPC- DADRI Salary- Rs. 80-k per month. Requirement is on urgent basis, prefer only those candidates, who can join immediately. *Interested can apply on my email id- ajaysharma@hlfppt.org or call me / WhatsApp @ 07982764663 Job description (Medical Officer-MBBS) Clinical assessment of the patients' medical/health problems by referring to their history and carrying out diagnosis, investigation, treatment for the stipulated period of time as mentioned. Provide Maternal, New born Child & Adolescent Healthcare including identification of high-risk pregnancies & appropriate referral. Proper counseling for quick referral, regular intake of medicines. Maintain confidentiality and impartiality of patients. Effective functioning of MHC, supervision of other staff functions. Reach & Leave timely from FSDP. Counsel patients about their illness or disease. Counsel patients about the dietary requirements as per their illness. Motivate them to have healthy and hygienic lifestyle. Take appropriate action for Bio Medical Waste Management with other staff. Counsel the patient about various communicable and non-communicable diseases. Counsel the patient about to preventive and curative measures of various seasonal, water and airborne diseases. Update to pharmacist about the medicinal requirement from time to time. Coordinate to paramedical team for insure their responsibilities. Submission of the monthly time sheet to Project Coordinator timely. Preparing the medicine indent and submitting it to the concern authority well in advance to avoid the scarcity of medicines. Any other task as assigned by Reporting Manager. Qualification : Relevant MBBS degree of recognized University. One of whom is preferably a lady doctor with maternal and child care specialization and experiences. About Project: HLFPPT shall be taking care of all the patients & provide Primary Healthcare, responsive to the needs of the people in the target villages around NTPC projects/stations. The basic objective is to provide Primary Healthcare, responsive to the needs of the people in the target villages around NTPC projects/stations. Provide maternal and child healthcare - antenatal/ prenatal & postnatal preventive healthcare to expectant & new mothers and new born babies & infants to effect reduction in Maternal Mortality Rate (MMR) and Neonatal Mortality Rate (NMR)/ Infant Mortality Rate(IMR) in project affected villages (PAVs) of NTPC stations & projects. To provide referral linkage to appropriate higher medical care facilities. To conduct Information, Education, and Communication (IEC) and Behavior Change Communication (BCC) to generate awareness on health and health related issues. *Interested can apply on my email id- ajaysharma@hlfppt.org or call me / WhatsApp @ 07982764663 Warm Regards, Ajay Sharma Sr. Manager- Human Resources 07982764663 For Hindustan Latex Family Planning Promotion Trust (A trust promoted by HLL Lifecare Ltd) 2nd Flr. HLL Life care Bldg., B/14-A,Sector-62, NOIDA-201301 T: +91 120 4673600 W: www.hlfppt.org

Job Description Job role Details: Nutrition Officer / Nutrition Senior Officer/ Nutrition Executive Qualification: Graduate/ Post Graduate (Science) Pls note that applicant should be open for relocation Roles & Responsibilities: The ethical promotion of Nestle's infant nutrition products in their territory by clearly communicating with Health Care Professionals (HCPs) about Nestle's Infant Nutrition products, their features, advantages, benefits and their appropriate use, within the Code of Ethics of Nestle's instructions and keeping in mind, mother's milk is best for Babies. Ensuring recommendation for the Nestle Nutrition product range within the scope of the Indian Code, detailing against homemade Paps and bovine milk. Being a reliable source of information on infant nutrition and infant feeding practices. Ensuring quality execution in terms of detailing/ conducting scientific symposiums etc. as per the company guidelines. Who can apply: Candidates who are graduates with at least 1 year of experience in nutrition or pharmaceutical industry. Candidates with high level of integrity & honesty, hardworking, self-motivator and passionate about enhancing quality of life and contributing to healthier future. Being able to work effectively in a team Ability to build strong and sustainable relationships High Learning agility Trustworthy and be able to work independently within the company policy & guidelines Nestle is committed to providing equal opportunities without any discrimination on the grounds of age, color, disability, origin, nationality, religion, race, gender, or sexual orientation. We are an equal opportunity employer, and we value diversity at our company. For any reasonable accommodation in the recruitment process for persons with disabilities, kindly reach out to your recruiter. Reasonable accommodation includes any appropriate modifications to ensure that persons with disabilities are provided an equal platform in the recruitment process.

Develop and lead research initiatives in areas of Computer Vision, Machine Learning and Natural Language Processing. Design, implement, and optimize computer vision algorithms to tackle real-world problems in content understanding and generation for improving marketing performance. Collaborate with product teams to turn research advances into impactful products. Develop scalable synthetic data generation and evaluation techniques. Train models and run experiments to study data and model quality. Iteratively refine research experiments and clearly communicate insights to the team. Integrate core machine learning models into the Adobe Experience Manager and Adobe Experience Platform. Collaborate with product, design, and engineering teams to rapidly prototype and transition conceptual prototypes from research to production. Requirements Proven expertise in one or more of the following areas: Computer Vision, Multimodal Content Understanding with Large Language Models and Agentic Workflows,. Multiple publications in top-tier conferences such as CVPR, ICLR, NeurIPS, ICCV, ECCV, ICML, ACL, EMNLP, KDD, etc. 4+ years of experience in computer vision research and product development PhD, MSc, or equivalent experience in Computer Science, Electrical Engineering, Robotics, or a related field. Hands-on experience and a track record of deploying solutions in production environments. Experience in deriving concrete conclusions and actionable insights from large datasets. Ability to take research risks and solve hard problems independently. You Will Thrive In This Role If You: Are a great teammate who is willing to take on a variety of tasks to contribute to the success of the team Have a proven track record and an impulse for empirical research, answering complex questions with data. Are capable of leading ambitious projects and possess clear communication skills. Have familiarity with crafting quality research experiments and evaluations with rapid iterations. Have experience working in complex technical environments, improving research velocity. Possess a flexible analytic approach that allows for results at varying levels of precision.

Develop and lead research initiatives in areas such as Natural Language Processing, Computational Social Science, Computer Vision, and Machine Learning. Collaborate with product teams to turn research advances into impactful products. Design challenging evaluations related to creative intelligence and marketing performance. Develop scalable synthetic data generation and evaluation techniques. Manipulate and analyze complex, high-volume, high-dimensionality data from diverse sources. Train models and run experiments to study data and model quality. Iteratively refine research experiments and clearly communicate insights to the team. Integrate core machine learning models into the Adobe Experience Manager and Adobe Experience Platform. Collaborate with product, design, and engineering teams to rapidly prototype and transition conceptual prototypes from research to production. Requirements Proven expertise in one or more of the following areas: Large Language Models, Computer Vision, Natural Language Processing, Computational Social Science, Behavioral Sciences, Agentic Workflows, Social Network Analysis, Causal Inference, Recommendation Systems, Multimodal Content Understanding. Multiple publications in top-tier conferences such as ICLR, NeurIPS, ICML, PNAS, Nature, Science, ACL, EMNLP, CHI, WWW, KDD, ICCV, ECCV, CVPR, etc. Hands-on experience and a track record of deploying solutions in production environments. Experience in deriving concrete conclusions and actionable insights from large datasets. Ability to take research risks and solve hard problems independently. BTech (for research associates) or PhD degree or equivalent experience (for research scientists) in industrial research in Computer Science, Statistics, Economics, or other relevant technical fields. For senior positions, a minimum of seven years of post-PhD experience is required. You Will Thrive In This Role If You: Are a great teammate who is willing to take on a variety of tasks to contribute to the success of the team Have a proven track record and an impulse for empirical research, answering complex questions with data. Are capable of leading ambitious projects and possess clear communication skills. Have familiarity with crafting quality research experiments and evaluations with rapid iterations. Have experience working in complex technical environments, improving research velocity. Possess a flexible analytic approach that allows for results at varying levels of precision. Have familiarity with relational databases and SQL. Bonus: Experience with large-scale data systems such as Beam or Spark.

Role & responsibilities Patient/ Customer Care 1. To provide expert consultation and manage all patients related to pediatrics with the knowledge of senior consultants. Job Knowledge 2. To keep abreast with latest research, development & techniques in the field of pediatrics Process Orientation/ Documentation 3. To conduct and supervise all tests / procedures related to pediatrics 4. To generate reports on test / procedures performed (Operation notes and discharge summary) 5. To ensure proper attention to the patient & their attendants. 6. To ensure that the wards / O.T. rooms have equipment / facilities necessary for rendering patient care as per availability. 7. To supervise all nursing / Para medical and non medical staff of the department to maintain discipline and high standard of medical care at the departments. 8. To provision infrastructure and maintenance support 9. To ensure optimum utilizations of resources by the him /her and subordinates 10.To have complete orientation of QMS and EMS system of Hospital. 11.To have complete Awareness about Disaster Management Programme (DMP) of the hospital. 12.To Comply with the service quality Process, environmental & occupational issues & policies of the respective area. 13.To Comply with patient safety policy. People Orientation 14.To coordinate with Head Of Department on all matters relating to: 15.To co-ordinate and contribute with the team for development of newer facilities 16.To proactive in terms of patient care (Planning and anticipation) 17.To complaint redresses of patients 18.To take part in all regular CMEs. Cost & Revenue 19. To select type and nature of medical consumables and equipment to be procured. Discipline 20. To be well groomed, punctual & adhere to company policies and practices.

We are hiring for apprentice role. Please find the required details below: Job Requirement: Qualification: Diploma in Medical Laboratory Technician (DMLT/ Bsc. MLT) Duration: 1 Year Benefits: Be a part of India's largest diagnostic chain. Career advancement opportunities. Rewarding Culture. NABL & CAP Accredited Labs. If interested, please share your resume on supriyakarkera@lalpathlabs.com

To participate in the general management and care of all patients including undertaking preliminary basis and routine investigations and treatment (pre-and post-operative care) under supervision. To see all new cases especially the seriously ill patient immediately upon admission and to initiate emergency treatment without delay. To ensure that all investigations and treatment prescribed are carried out and reviewing cases daily or more frequently including reviewing the results of investigations and treatments. To oversee the proper documentation of patients management from admission to discharge. To ensure clarity of plan of care for each patient is documented on a daily basis. To prepare a comprehensive discharge summary for each patient which is authenticated by a consultant. To update case notes and complete all case records within 24 hours of the patients discharge. For inquiries, kindly reach out to - Mr. Puneet Sharma, at 8368229903, 8860813169 or at puneet.sharma1@fortishealthcare.com

Role & responsibilities - Day to day activities in OHC Preferred candidate profile - For Kolar Region Perks and benefits - As per the market standard

Must be willing to work in US rotational shift Must be willing to work from Office Any Nursing Graduates BSc Nursing/ Msc Nursing & Post Bsc Nursing) Office - Chamundi towers –Global Village - Kengeri

To offer consultation & patient diagnosis, perform/supervise all medical procedures of Dermat Led services ensuring efficacy, safety & high professional standards of medical procedures carried out under your supervision. Required Candidate profile Consultation & Patient Diagnosis Perform doctor led services Candidate must be MD or DVD or DDV or DNB in Dermatology Lucrative incentive will also be given CONTACT-Ishan/Neetu 9910796268/7838473883 Perks and benefits Leaves & Incentives as per company policy

Title: PV Scientist - Senior ExpertLocation: Bangalore Purpose of the Role: We are seeking a highly motivated and skilled Pharmacovigilance Scientist to collaborate with global safety leads and program safety leads This role is essential for providing integrated medical safety strategies for assigned investigational and core (high-risk) marketed products, including input into safety aspects of clinical development, risk management, and benefit-risk management Your roleSignal Detection and Management:Perform safety monitoring using dedicated tools (eg, Spotfire, EVDAS, Empirica Signals) for signal detection Review and analyze clinical and safety database outputs; interpret aggregate safety data from clinical trials and post-marketing sources Review scientific literature for safety surveillance and signal detection Support the analyses of safety signals, contribute to authoring signal evaluation reports, and participate in relevant safety governance meetings Support communication of findings from Emerging Safety Issue Reports to external stakeholders RMP Updates and Periodic Safety Reports:Retrieve/summarize data from various sources in support of authoring and providing content for Risk Management Plans (RMPs) and periodic safety reports Support local adaptation of RMPs and respond to health authority questions Submissions and Safety Variations:Contribute to delivery of safety relevant documents of the Common Technical Document (CTD) Contribute to ISS/SCS IAP, health authority briefing documents, and product information and clinical overview addendum Clinical Trial Activities: Provide input into safety sections of the Investigational Medicinal Product Dossier (IMPD), Investigators Brochure (IB), and Informed Consent Form (ICF) Support delivery of safety-related input for clinical trial documents, including protocols and reports Provide safety related input for data monitoring committees with safety-related documentation Other Activities:Respond to queries from auditors/inspectors and participate in interviews Contribute to the design and implementation of post-authorization safety studies Develop and maintain MedDRA CMQs for signal analysis and aggregate safety data Create product-specific training for internal and external stakeholders Provide expert input into process standardization and improvement within GPS and GD Who you are: Experience Required:MD, or PhD/advanced science degree or tertiary level qualifications in a biomedical/health related field Fluent in written and spoken English Qualification:Over 4 years of Pharmaceutical industry experience or similar (egHealth Authority) Experience in Pharmacovigilance risk management in both clinical development and post-marketing areas, including submission experience Ability to work collaboratively in a global team environmentTech savy with strong analytical and communication skills

Exciting Opportunity for Doctors! We are thrilled to announce an opening for Doctors at Raipur Multi-specialty Hospital, If you're a dedicated and passionate doctor looking to make a difference in your role, we want to hear from you! 1. Interventional Cardiologist 2. Urologist 3. Nephrologist Experience 2 to 8 years in after PG (lesser experience Consultants are mentioned separately) Need doctors from the specified institutes / hospitals. - candidates from corporate setups are needed . • Placement of Consultants on Minimum Guarantee no private OPDs will be allowed, also the Consultants have to provide their services ONLY to Hospitals. Salary will not be a constraint and will depend on Qualifications and Experience. Use of HMIS in OPDs & IPDs mandatory. Proficient in Hindi communication. Work : Location Raipur. Interested candidates can share their CVs at s.sourabh@randstad.in or can connect in 8809510027 Best Regards,

The Senior External Data Specialist (SEDS) is responsible for providing technical, procedural (SOPs) and planning leadership across multiple projects assigned to the external data group team members ensuring that they deliver in accordance with SOPs, programming best practices, and the timelines agreed within the Project Team. Scope external study data requirements and effort for projects. Project manage all external data related activities across multiple projects. Provide expert advice on the transfer and expected formats of data transfer files. Provide technological expertise and guidance on the best methods for handling laboratory data and other external data. Create and maintain data transfer agreements. Maintain study documentation within project files as appropriate. Act as primary contact and study representative to third party data providers. Effectively communicate transfer requirements and project timelines to various stakeholders. Identify and communicate project risks. Ensure data integrity is maintained by implementing appropriate data controls for masked data. Ensure delivery of timely data transfers and undertake quality reviews and testing activities. Conduct external data reconciliation using available technologies and processes. Raise queries to external data providers and track queries to successful resolution. Provide listings to medical review team. Assess and implement new data review and analysis processes and technologies. Take a lead role in the development of best practices, process improvement, quality control and governance related to all external data matters. Provide training and mentoring to team members in SOPs, software applications, and best practices. Attributes and Skills-Expert domain knowledge and experience within clinical research and drug development. Advanced knowledge in >1 EDC systems and laboratory processes. Experience mentoring and training others. Awareness of regulatory and compliance issues and understanding of application of SOPs and Quality Control to daily activities. Excellent analytical, communication and problem-solving skills. Responsibilities The Senior External Data Specialist (SEDS) is responsible for providing technical, procedural (SOPs) and planning leadership across multiple projects assigned to the external data group team members ensuring that they deliver in accordance with SOPs, programming best practices, and the timelines agreed within the Project Team. Scope external study data requirements and effort for projects. Project manage all external data related activities across multiple projects. Provide expert advice on the transfer and expected formats of data transfer files. Provide technological expertise and guidance on the best methods for handling laboratory data and other external data. Create and maintain data transfer agreements. Maintain study documentation within project files as appropriate. Act as primary contact and study representative to third party data providers. Effectively communicate transfer requirements and project timelines to various stakeholders. Identify and communicate project risks. Ensure data integrity is maintained by implementing appropriate data controls for masked data. Ensure delivery of timely data transfers and undertake quality reviews and testing activities. Conduct external data reconciliation using available technologies and processes. Raise queries to external data providers and track queries to successful resolution. Provide listings to medical review team. Assess and implement new data review and analysis processes and technologies. Take a lead role in the development of best practices, process improvement, quality control and governance related to all external data matters. Provide training and mentoring to team members in SOPs, software applications, and best practices. Attributes and Skills Expert domain knowledge and experience within clinical research and drug development. Advanced knowledge in >1 EDC systems and laboratory processes. Experience mentoring and training others. Awareness of regulatory and compliance issues and understanding of application of SOPs and Quality Control to daily activities. Excellent analytical, communication and problem-solving skills.

The position will be responsible for development of assigned project within given timeframe as per safety and environmental rules. This includes thorough literature survey, bench scale trials, preparation of SOPs, necessary documentation. This would also include Demo of developed chemical process to PD team, support in KL, pilot plant and commercial plant for successful technology transfer. Strategic Responsibilities To understand the objective of project / chemistry / MSDS Search the additional literature as required. Inputs in planning of experiments/ man power / glassware/ raw materials/ analysis To ensure proper maintenance of lab equipment s. Proper house- keeping and use of PPE s. Use relevant MSDS for safe handling and disposals of toxic chemicals Operational Responsibilities Bench scale experiments as per planning and Identification of critical parameters Co-ordination with QC for analytical support / development and Prepare sample as per required quality Optimization of process w.r.t. identified critical parameters and Impurities characterization and synthesis. Understanding the parameters responsible for impurities. Process validation by reproducing min. three consecutive batches. Experimental observations and data compilation Demo batches to PD To check quality plan/ Plant SOP and Use test of RM s Data compilation and time to time update of KL/ PP plant trials Financial Responsibilities Contribute to budget proposals. Contribute to budgetary controls within the area of responsibility. People Responsibilities Utilization of all available sources for skill up-gradation Actively participation in problem solving sessions/ training programs Coordination and communication with team To guide subordinates Education Qualification Master and PhD in Organic Chemistry from a reputed University / Institute Work Experience 0-8 years of Industrial Experience. Industry to be Hired from Agro chemicals/fine chemicals/ pharma-API/ Specialty chemicals. Functional Competencies Route Scouting Literature Search Practical Experience of Lab working Understanding of HSE Data Management Analytical data interpretation

The Position will be responsible for development of assigned project within given timeframe using new Technology. This includes thorough literature survey, bench scale trials, preparation of SOPs, necessary documentation. This would also include Demo of developed chemical process to PD team, support in KL, pilot plant and commercial plant for successful technology transfer. Strategic Responsibilities To understand the objective of project / chemistry / MSDS Search the additional literature as required. Inputs in planning of experiments/ glassware/ raw materials/ analysis To ensure proper maintenance of lab equipments. Proper house- keeping and use of PPE s. Use relevant MSDS for safe handling and disposals of toxic chemicals Operational Responsibilities Development of processes using flow chemistry (Micro /Meso reactors). Mapping the suitable reactor & pumps for development of process in Flow Technology Finding out suitable equipment for downstream operation for continuous manufacturing. To generate data for carrying out scale-up study using Design of Experiment mechanism To ensure seamless efficient scale-up of the process developed by working closely with Process Chemist team. To identify the cost reduction opportunities in the projects already running at commercial scale using flow technology. Drive optimum utilization of all available resources Financial Responsibilities Actively participate in problem solving sessions/ training programs and drive coordination and communication within the team Ensure on time delivery of assigned project in terms of: On time delivery with target yield and quality. Waste minimization Smooth scale-up up to KL/PP Ensuring the safety & house keeping Inspire & motivate employees through demonstrated commitment to PI s values, vision & mission and exemplifying effective leadership, initiative and persistence needed to accomplish goals and objectives Drive collaboration and cross-functional networking for the entire team People Responsibilities Foster an environment of knowledge sharing within the Team Maintain healthy working relationships with the related teams and departments. Education Qualification Master/Doctorate in Organic Chemistry from a reputed University / Institute Work Experience 0-8 Industrial Experience. Industry to be Hired from Agro chemicals/fine chemicals/ pharma-API/ Specialty chemicals Functional Competencies Experience in Flow Chemistry/Technology Practical Experience working on Flow reactors (Static and Dynamic) Experience in handling different types of Pumps Documentation, report writing and familiar with MS office suite Data Management Analytical data interpretation

The Position will be responsible for formulation development, prepration of sample and to provide basic data to supervisor for smooth functioning of formulation development activity This would include arrangement of raw material/ material from store, maintain equipment/ instrument and records as per requirement To maintain good House keeping and 5S activity in lab Strategic Responsibilities Maintain document/ record for trials conducted. Participation in the meetings & provide inputs as & when required by Deptartment head. Operational Responsibilities RM Arrangement from store Calculations for execution of experiment Conducting trials as per supervisor instruction and maintanin its record/observation Provide backup calculation & data for Experiments Equipment handling and maintenance Financial Responsibilities . People Responsibilities To attend training programs for safety, equipment/instrument handling Coordination with kilo lab / pilot plant/ R&D / QC for day to day activity Ensure smooth working of the department to maintain high morale of the workforce Education Qualification M.Sc Chemistry (Preferred Agrochemical and Pesticides) Work Experience 0 3 years Industry to be Hired from Agrochemical / Chemical Functional Competencies Knowledge of the major formulation types used in agrochemicals (EC, SC, OD, SL, WDG, WP) etc. Research Approach Conducting trials in the kilo/pilot plant. Broad knowledge of experimental chemical techniques with background knowledge of formulation development within the crop protection industry

Role & responsibilities Patient Care: Provide comprehensive medical care to women, including routine check-ups, prenatal care, and postnatal care. Diagnosis and Treatment: Diagnose and treat gynecological conditions such as infections, diseases, and disorders of the reproductive system. Surgical Procedures: Assist in gynecological surgeries, including minimally invasive procedures, as required. Labor and Delivery: Manage and assist in labor and delivery, ensuring the health and safety of both mother and baby, ANC cases & high risk pregnancy. Patient Education: Educate patients on reproductive health, contraception, and preventative care. Medical Records: Maintain accurate and up-to-date medical records for all patients. Collaboration: Work closely with other healthcare professionals to provide integrated care. Emergency Care: Provide emergency care and treatment when needed. Follow-Up Care: Conduct follow-up visits to monitor patients' health and progress. Continuing Education: Stay updated with the latest medical research and advancements in gynecology. Preferred candidate profile Education: MBBS with a specialization in Gynecology (MS/MD/DNB). Experience: 0-5 years of experience working as a gynecologist . Perks and benefits Best in the Industry

Long Description Primary Job Responsibilities: Method development, qualification and transfer and data review activity. Analyst training, CSV lab compliance and lab support. Additional Job Responsibilities: Coordination with DQA for compliance and documentation activities. Competencies Collaboration Customer Centricity Developing Talent Innovation & Creativity Process Excellence Result Orientation Stakeholder Management Strategic Agility Education Masters in Biotechnology or Biochemistry Work Experience Candidate with 10-12 years of experience in chromatographic method development and qualification

Job Purpose The prospective candidate shall handle Payments Advisory covering the following products: Wallets - Prepaid Payment Instruments (PPI), Payment Aggregator (PA), Payment Gateway (PG), Bharat Bill Payment System (BBPS) and UPI. Review RBI reporting on PPI and other returns. Required Qualifications and Experience Educational Qualifications Preferred qualification - CA / CS/ MBA- (Finance) Work Experience Experience in handling Wallet, PA, PG, BBPS transactions in a reputed bank/ financial institution. Knowledge of RBI Master Directions on Issuance and Operation of Prepaid Payment Instruments and Know Your Customer. Understanding of other relevant laws and regulations. Excellent communication (written - oral) and report writing skills. Reasoning and analytical skills required for Fraud Monitoring and Reporting. Strong desire to initiate and execute in high paced growing environment. Should be a self-starter and a team player.

Long Description Primary Job Responsibilities: Structural and functional characterisation of proteins using LC-MS Expertise in Impurity characterization by LC-MS Data analysis and review for Bio similarity assessment Having a experience to advanced LC-MS applications and DQA SOPs. Planning of characterization experiments using LC-MS Drafting and/or review reports and presentations on experimental data and scientific outcomes for CMC / RA for dossier submission. Drafting of scientific study protocols and reports related to method development, method qualification, assessing bio similarity etc. Guiding and mentoring team members sample preparation, LC-MS workflows and data interpretation. Support cross-functional analysis such as charge variant and impurity characterization. Review the MS data and documentation of analysis performed and result reporting Method Development, Qualification report preparation Competencies Collaboration Customer Centricity Developing Talent Innovation & Creativity Process Excellence Result Orientation Stakeholder Management Strategic Agility 1. Strategic Agility 2. Innovation & Creativity 4. Developing Talent Adaptability/Flexibility Education Masters Doctorate in Biotechnology Work Experience Experience: 7-9 yearsof experience in protein characterization .

BVG India Ltd. is looking for Staff Nurse to join our dynamic team and embark on a rewarding career journey Provides patient care and administers medications Assists doctors in medical procedures Monitors patient recovery and health conditions Maintains accurate medical records

Position - Lab Technician Location - Mumbai Qualification Required- DMLT/ BSc MLT Experience- 1- 5 years Role & responsibilities To perform assigned analytical testing procedures in an accurate, precise, and timely manner in the assigned lab. To perform routine and non-routine activities pertaining to laboratory testing and reporting and maintaining external and Internal Quality control Maintain required records and documentation. Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result. Analyze specimens using approved testing procedures as per SOP's, review and release test results. Adhere to the laboratory's quality control policies, instrument and procedural calibrations and follow safety guidelines as per established organization protocols. Interested Candidates can share their resume at Supriya.karkera@lalpathlabs.com