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“India has one of the largest railway networks in the world. Around 1.3 million persons are employed in Indian Railway. This article talks about the salary of employees working in Indian railway.”Indian Railways is the largest railway network in Asia and the world’s second largest single entity employer. With over 1.3 million employees, the Railways is the largest public utility and commercial service in the country. This web section provides detailed information on Indian Railways salaries and allowances, especially after pay revision in line with recommendations of the 7th Pay Commission.Group-wise Railway Pay Band & Grade Pay OverviewGroupPay BandPost NameGroup-A8700 to 10000Manager, General ManagerGroup-B4800 to 7600Chief Yard Master, Station Supervisor and othersGroup-C2000 to 4600Junior Engineer, Loco Pilot, Train Ticket Examiner, Reservation cum Ticketing Clerk & othersGroup-D1800 to 1900Track Man, Helper, Track Maintainer and othersRailway Group C & D Salary StructuresThe following table details Group C & D Railway Employees Salary Structure. Railway’s front operation, train running and track maintenance, train and track security, electric supply, etc. The table gives entry level salary data for each post.PositionPresent GPNew Salary (Start Level)New LevelSpecial Running Staff AllowanceLoco Pilot (Shunting)42003540061125Loco Pilot (Mail)42003540062250Loco Pilot (Pass/Motorman)42003540061125Loco Pilot (Goods)4200354006750Shunter Gr I4200354006750Shunter Gr II2400255004750Senior Fireman-I, Senior Assistant Loco Pilot2400255004Fireman-I, AssistantLoco Pilot1900199002Senior Second Fireman1900199002Second Fireman1800180001Gangmate2800292005Keyman2400255004Head trackman2400255004Sr Trackman2400255004Trackman2400255004Train Clerk1900199002Sr Safaiwala Jamadar2400255004Safaiwala Jamadar2000217003Technician Gr-III1900199002Technician Gr-II2400255004Technician Gr-I2800295005Sr Safaiwala1900199002Safaiwala1800180001Traffic Running StaffGuard M/E4200354006Sr. Pass Guard4200354006Sr.Goods Guard4200354006Goods Guard2800292005Sr Assistant Guard2400255004Assistant guard1900199002Railway Commercial Staff New SalaryThe Commercial staff of Railways is taking care of issuing of tickets, reservations, cancellations, handling enquiries and also checking tickets in trains and at stations. The Commercial staff category include:Commercial ClerkReservation cum Ticketing ClerksEnquiry ClerksTTEs and TCsExisting Grade PayRecommended New Grade PayNew Matrix LevelNew Salary190020003217002400280052920042006354004600744900Indian Railway Accounts Cadre New SalaryAccounting is the back office operation of Railway. They handle the revenue operations of the organization.PositionPresent GPNew Matrix LevelNew SalaryAccounts Clerk1900219900Jr Accounts Assistant2800529200Accounts Assistant4200635400Sr Section Officers/Sr Travelling Inspector A/cs/ Sr Inspector of Stores Accounts4800*847600* The Commission has recommended that those in the GP of 4800 completed four years should be upgraded to GP 5400.RRB Salary for RPF (Police) and Engineering StaffPost NameDepartmentGrade PayPay BandPay ScaleRPF ConstableRPF/RPSF₹ 2,000PB-1₹ 5,200-₹ 20,200Assistant Sub-Inspector (Police)RPF/RPSF₹ 2,800PB-1₹ 5,200-₹ 20,201Head ConstableRPF/RPSF₹ 2,400PB-1₹ 5,200-₹ 20,202Inspector (Police)Civil / Mechanical / Electrical / Engineering Department /Stores Department₹ 4,600PB-2₹ 9,300-₹ 34,800Section EngineerCivil / Mechanical / Electrical / Engineering Department /Stores Department₹ 4,600PB-2₹ 9,300-₹ 34,800Loco Inspector/ Section EngineerCivil / Mechanical / Electrical / Engineering Department /Stores Department₹ 4,600PB-2₹ 9,300-₹ 34,800Chemical & Metallurgical Superintendent Gr .IICivil / Mechanical / Electrical / Engineering Department /Stores Department₹ 4,600PB-2₹ 9,300-₹ 34,800Depot Materials SuperintendentCivil / Mechanical / Electrical / Engineering Department /Stores Department₹ 4,600PB-2₹ 9,300-₹ 34,800Shipping InspectorCivil / Mechanical / Electrical / Engineering Department /Stores Department₹ 4,600PB-2₹ 9,300-₹ 34,800Commercial SuperintendentCommercial₹ 4,600PB-2₹ 9,300-₹ 34,800Sr. Commercial ClerkCommercial₹ 4,600PB-2₹ 9,300-₹ 34,800Chief Ticket InspectorCommercial₹ 4,600PB-2₹ 9,300-₹ 34,800Chief Enquiry & Reservation SupervisorCommercial₹ 4,600PB-2₹ 9,300-₹ 34,800Law AssistantCommercial₹ 4,600PB-2₹ 9,300-₹ 34,800Chief Catering InspectorCommercial₹ 4,600PB-2₹ 9,300-₹ 34,800Dy. Station SuperintendentCommercial₹ 4,600PB-2₹ 9,300-₹ 34,800Headmaster/Head mistress/ higher secondary school/Intermediate CollegeEducation₹ 7,600PB-3₹ 15,600-₹ 39,100Principal/Head Master (Secondary/High School & equivalent) Group ‘B’ GazettedEducation₹ 7,600PB-3₹ 15,600-₹ 39,100Indian Railway Medical Officers and Paramedical SalaryThrough Indian Railways Medical Services the railway provide health delivery services to all stakeholders including passengers and railway staff. Railway’s healthcare infrastructure is equipped to provide healthcare to railway passengers who fall sick during journey, those who meet with accident while on travel or within railway property, and also include complete medical facility to all railway staff and their families.Post NameDepartmentGrade PayPay BandPay ScaleGeneral Duty Medical OfficerIRMS₹ 5400PB-3₹ 15600-₹ 39100Specialist/SurgeonsIRMS₹ 6000PB-3₹ 15600-₹ 39100Dental SurgeonIRMS₹5400PB-3₹ 15600-₹ 39100Assistant Nursing Officer( Group ‘B’ Gazetted)Medical₹ 5,400PB-3₹ 15,600-₹ 39,100Staff Nurse (Group ‘C’)Medical₹ 4200PB-2₹ 9300-₹ 34800Lab Supdt. Gr. IMedical₹ 4,600PB-2₹ 9,300-₹ 34,800Sr. DieticianMedical₹ 4,600PB-2₹ 9,300-₹ 34,800Some other allowances that are given to RRB Employees along with Salary:Daily Allowance along with Mileage Allowance for local journey beyond 8 kmDearness Allowance (DA)House Rent Allowance (HRA)Transport Allowance (TPA)Night Duty AllowanceFixed Conveyance AllowanceConveyance Allowance to DoctorsCompensation in lieu of HolidaysSpecial Compensatory (Tribal/Scheduled Area) Allowances.Special Allowance to Railway School TeachersSpecial Allowance for Child care for women with disabilities and Educational AllowanceOvertime Allowance (OTA) and othersAbout Indian RailwaysIndian Railways is a public enterprise completely owned and administered by the Indian Government.The Railway Ministry oversees the operations of seventeen zones of Indian Railways that are further sub-categorized into 68 divisions. Indian Railways has the fourth-largest railway network in the world with an estimated total track length comprising 1, 15, 000 kms. It is also the largest employer in India and the ninth largest in the world with more than 14 lakh employees.Each and every zone is under the supervision of a GM (general manager) and each of the 68 divisions which fall under a specific zone is controlled by a DRM (divisional railway manager). Every division has several departments headed by a chief (chief commercial manager, chief electrical engineer and so on) who directly report to the DRM. Like all central government employees, railway staffs enjoy a high salary with numerous perks and incentives. They’re also entitled to receive pension after superannuation.Classification of Railway ServicesRailway posts across all departments (like commercial, electrical, operations, traffic, engineering, and so on) are basically classified into two categories: – Gazetted Posts (Group ‘A’ and Group ‘B’) and Non-Gazetted Posts (Group ‘C’ and Group ‘D’ and staff engaged in different workshops). As the table below clearly illustrates, all positions classified under Groups A and B have higher pay scales than posts stratified under Groups ‘C’ and ‘D’. Consequently, the basic salaries for posts under Groups A and B are also more.Indian Railway Salary SlipIndian Railway employees can login to Indian Railway Employee Information System – the official website of railway employees to download their salary slip. To get access employee need to provide his/her unique ID and password. In IREIS one can view monthly pay slip, leave details, provident fund details and other service related information. Various private websites also provide railway salary tables, but they are not authentic.

Short answer: Conventional wisdom characterized Th1 as T cells that secrete mainly IFN-g, TNF-a, LT-b and Th2 as those that secrete mainly IL-4, IL-5, IL-6, IL-9, IL-10, IL-13 (1). However, it's becoming increasingly clear that the Th1-Th2 paradigm is perhaps outmoded, that CD4 helper T cells remain highly plastic in their effector functions, and that, following activation, they evolve particular sets of overlapping functionalities with distinct underlying transcriptional programs, and that they retain capacity for reprogramming.Long answerIn order to to fully understand how we ended up with our current understanding of CD4 helper T cell biology, we need to start from the beginning. How did the Th1-Th2 paradigm start? Why did it catch on? How did it evolve and how do we use this paradigm today? Finally, is this paradigm still useful or do its flaws make it more an impediment?How did the Th1-Th2 paradigm start?This paradigm starts with Mosmann et al's 1986 Journal of Immunology paper (2). First, they created a large number of CD4 T cell lines in vitro by repeatedly stimulating them with antigens such as FGG (Fowl Gamma Globulin) and KLH (Keyhole Limpet Hemocyanin), and then cloned them. With these CD4 T cell clones in hand and using a variety of bioassays, Mosmann et al showed two things.Dichotomy in the cytokines secreted by these CD4 T cell clones.Those that secreted IL-2 did not secrete IL-4 and vice-versa. They called the former Th1 and the latter Th2.Apparently stable imprinting of the mutually exclusive cytokine secretion pattern. They stimulated the CD4 T cell clones with a polyclonal stimulus called Concanavalin A, and found similar dichotomy in the pattern of cytokines secreted, i.e. even when these T cells were stimulated very strongly with something else, they retained the same pattern of cytokine secretion.At this time, ability to detect cytokines was very limited because there were hardly any cytokine-specific monoclonal antibody (Mab) pairs for ELISA (Enzyme Linked ImmunoSorbent Assay). Subsequent expansion of such tools led to improved characterization of CD4 helper T cell subsets.So far, so good. However, the question remained as to the biological relevance of this apparent in vitro dichotomy in CD4 helper T cell biology.Why did the Th1-Th2 paradigm catch on?The Th1-Th2 paradigm was originally an in vitro observation. It caught on when Heinzel et all showed an apparently similar dichotomy in vivo in their 1989 Journal of Experimental Medicine paper (3). They examined CD4 T cells using the experimental mouse model of leishmaniasis (a protozoan parasite with a complex life cycle spanning sand flies and mammals). Since the 1970s, it was known that a particular inbred mouse strain called BALB/c is exquisitely susceptible to Leishmania major infection while other inbred strains such as C57Bl/6 are relatively resistant. Heinzel et al observed T cells from infected susceptible BALB/c mice secreted abundant IL-4 and little IFN-g, a pattern opposite to those from infected resistant C57Bl/6. With this in vivo mouse model observation, here was proof positive about the existence of Th1 and Th2 subsets!From reference 4.The early promise of this so-called in vivo proof of the Th1-Th2 paradigm never quite panned out. For example, one of the early predictions from this paradigm was that the IL-4 gene knock out would convert the susceptible BALB/c mouse to resistance. Two groups independently created BALB/c IL-4 knock-outs and duly challenged them with Leishmania major. Utter confusion ensued. One IL-4 knock out BALb/c mouse strain apparently remained susceptible (5) while another apparently became resistant (6). What gave? All sorts of things including different gene knock out strategies, different parasite strains, different parasite doses used for infection, and on and on. In short, biology isn't easily boxed into neat dichotomies. As it turns out, far from being a puzzle so easily cracked, the Leishmania major susceptibility of the BALB/c mouse strain remains an active area of research till date.How did the Th1-Th2 paradigm evolve and how is it used today?The primary influence of the Th1-Th2 paradigm was in imposing a particular mental construct with respect to our understanding of CD4 helper T cell biology. For example, in the mid-1990s, while examining gut-associated CD4 helper T cells, Howard Weiner observed some of them secreted neither IFN-g nor IL-4 but rather abundant TGF-b1. Naturally, he assigned the label Th3 to such cells (7). Few years later, other immunologists identified CD4 T cells that primarily secreted IL-17A. No prizes for guessing the name we bestowed upon them (8). Th17 of course!At this point it's worth our while to take stock of the technological advances that helped evolve and solidify the paradigm of Th1, Th2 and other CD4 T helper cell subsets.In 1993, the long-sought CD4 T cell co-stimulator molecule was identified as CD28 (9).Starting in the 1990s and continuing till date, Mab pairs against all kinds of protein molecules started to become easily available.Similarly, biotech companies such as RandD, Invivogen, Invitrogen, etc started to synthesize and make available to the research community a wide variety of recombinant cytokine molecules.Capitalizing on the increasing availability of Mabs against a plethora of protein molecules, biotech companies such as Miltenyi Biotec, Dynabeads, and more recently Stemcell Technologies developed a variety of immunomagnetic cell isolation procedures that enabled easy enrichment of CD4 T cells from secondary lymphoid organs and blood.If purity of cells enriched by immunomagnetic separation were insufficient, there was the alternative Flow cytometry Sorting approach using the Flow cytometer and Mabs which yielded highly pure cell subsets.1, 2, 3, 4 and 5 helped launch a plethora of imaginative in vitro CD4 helper T cell culture techniques. How? Seemingly simple. Isolate T cells using methods 4 or 5, and stimulate them in vitro with anti-CD3 and anti-CD28 Mabs plus the magic sauce to drive them to differentiate into either Th1 or Th2. T cells require two signals, Signal 1 (targeting the T cell receptor) and Signal 2 (co-stimulator), for activation. In this in vitro approach, a Mab against the CD3 molecule serves as a surrogate for Signal 1, while a Mab against the CD28 molecule serves as a surrogate for Signal 2. The magic sauce? Over the years, by adding a variety of recombinant cytokines and Mabs, labs around the world evolved a variety of complex protocols to stably generate in vitro Th1 and Th2 cells. For example, stimulate with anti-CD3 and anti-CD28 Mabs plus anti-IL-4 Mab (to inhibit differentiation to Th2) and recombinant IL-12p70 (or IFN-g) to promote Th1 differentiation, to give one example.In concert with cell culture techniques described in 6, molecular biology approaches evolved apace. Such were applied to these so-called Th1 and Th2 cells to explicate their molecular signatures. Thus, the transcription factor T-bet was found primarily associated with capacity of T cells to secrete IFN-g (10) while another transcription factor GATA-3 was found primarily associated with capacity of T cells to secrete IL-4 (11).Mouse gene knock-out studies followed, for both cytokines and their purported molecular transcription factor drivers. Such confirmed the association of specific transcription factors with specific CD4 T cell cytokines. In addition to IFN-g with T-bet and IL-4 with GATA-3, today we have additional associations such as IL-17 with ROR-gt and T regulatory cells (Treg) with FoxP3.In sum, the Th1-Th2 paradigm helped establish a seemingly impregnable mental construct whereby we envisaged CD4 helper T cell function to be non-overlapping or mutually exclusive or even antagonistic secretion of particular groups of cytokines, with different effector functions. This is why today in addition to Th1 and Th2, we have Th3, Th9, Th17, Treg, and so on.Is the Th1-Th2 paradigm still useful or do its flaws make it more an impediment?Almost from the beginning, there was pushback to the simplistic subsetting of CD4 helper T cell function along the lines of Th1, Th2 et al.Already in the 1990s, Anne Kelso, an Australian immunologist, developed some exquisite in vitro micromanipulation approaches (12, 13) to ask a really interesting question about CD4 helper T cells. Did daughter CD4 helper T cells display the same cytokine expression pattern as the parent? She cultured single CD4 helper T cells in Terasaki wells, stimulated them to proliferate, split the daughter cells into separate wells by micromanipulation, and compared parent and daughter cell cytokine expression patterns. Her results? Contrary to the established Th1-Th2 paradigm, she found daughter CD4 T cell cytokine patterns were not imprinted but rather stochastic. In other words, under the culture conditions she used, a parent CD4 T cell predominantly expressing IFN-g was no guarantee that its daughter T cells would behave the same. However, so powerful had the Th1-Th2 paradigm become that she switched to studying CD8 T cells instead. Ah, such is the impartiality and objectivity that undergirds our modern scientific enterprise!Almost from the beginning, the neat dichotomies of mouse CD4 T cell subsets refused to pan out so cleanly for human CD4 helper T cells. As a result, human immunologists accepted the Th1-Th2 paradigm either grudgingly or skeptically or not at all.Ah, those deceptively powerful in vitro cell culture techniques that helped define all these CD4 T cell subsets. Let's examine some of their flaws.a) Most studies used anti-CD3 (Signal 1) and anti-CD28 (Signal 2) Mabs to stimulate T cells in vitro. Obviously, this is not how our T cells get activated in vivo. So which in vivo scenario do such antigen presenting cell (APC)-free stimulations simulate? For one thing, these Mabs drive a much higher avidity interaction, something we rarely observe when T cells interact with their cognate antigen peptide presented inside an MHC class II molecule by APCs like dendritic cells (DCs), a cell-replete stimulation. Let's add to this other variables such as different Mab clones, different Mab concentrations, soluble, plate-bound or bead-bound Mabs. You see where I'm going? Given the variety of approaches used by different labs, it's practically impossible to compare data. At any rate, Mab stimulation of T cells is incontrovertibly an artificial system and exactly how it relates to in vivo CD4 T cell stimulation is unknown and perhaps more importantly, unknowable. Yet this has been the dominant approach in identifying and defining the variety of CD4 helper T cell subsets we are today familiar with from Th1 and Th2 to Treg, Th17 and TFH (more about this subset below).b) We use a variety of recombinant cytokines to drive CD4 helper T cells to differentiate in vitro into Th1, Th2, Th17, Treg and so on. Again, obviously, recombinant cytokines are artificial and absent in vivo.c) The absurdity of using anti-cytokine Mabs such as anti-IFN-g or anti-IL-4 in in vitro CD4 helper T cell differentiation protocols. Again, how b and c relate to the in vivo CD4 T cell differentiation program is unknown and perhaps more importantly, unknowable. And yet, we have thousands if not tens of thousands of peer-reviewed papers that have used precisely such cell culture approaches to help define Th1, Th2 et al.Where in the CD4 helper T cell subset universe do we slot the T Follicular Helper Cell (TFH)? T Follicular what? Well, you see, given our zeal for CD4 helper T cell subsetting, we immunologists found yet another CD4 T helper subset in the T cells that move into the B cell follicle to help B cells secrete high-affinity, class switched antibodies. After all, we refer to CD4 T cells as helper T cells precisely because they help B cells, CD8 T cells and macrophages develop and manifest their respective effector functions right?Expressing unique cell surface molecules such as ICOS, CXCR5 among others and unique transcription factors such as Bcl-6, c-maf, etc, and secreting additional cytokines such as IL-5, IL-6 and IL-21, the biggest surprise about Tfh cells was their plasticity (14, 15), in terms of capacity to express cytokines long corralled behind the mutually exclusive Th subset constructs. Could Tfh express IFN-g? Why yes! Could they express IL-4? Why yes! And so it went.In hindsight, it's hardly surprising that the so-called Tfh retained the capacity to secrete a wide variety of cytokines. After all, we know from mouse gene knock-out studies that IFN-g is a switch factor for IgG2a. In other words, a B cell switches from IgM to IgG2a after interacting with a cognate (specific for same antigen) CD4 T cell that secretes IFN-g. So much for the erroneous classifications that persisted for years and insisted on defining Th1 cells as indicative of so-called Cellular immune responses and Th2 cells as indicative of so-called Humoral immune responses!Different CD4 helper T cell cytokines are necessary to help B cells switch from secreting IgM to other high-affinity antibodies including a variety of IgGs, IgA and IgE. Examined in this fashion, is it not reasonable to assume that migrating into a B cell follicle to help a cognate B cell, an activated CD4 helper T cell should retain its capacity to secrete a variety of cytokines, IFN-g to help the B cell switch to IgG2a, IL-4 to switch to IgG1 and IgE, IL-17A to switch to IgG2b, TGF-b1 and IL-6 to switch to IgA, IL-5 to enhance capacity for antibody secretion per se, and IL-21 to help the B cell become a plasma cell, etc? Seen in this light, don't the non-overlapping CD4 T cell subsets we envisaged appear rather incongruent?Well, how do we envisage CD4 helper T cells develop their effector functions? One hypothesis (16) could be that the location (the tissue site) of the immune response is a key determinant in directing and guiding the ensuing CD4 helper T cell effector function. This, for two reasons primarily. One, the tissue has a vested interest in ensuring, over evolutionary time, that immune responses taking place within its environs do minimal damage to it. Two, most pathogens perforce evolve select portals of entry and tissue tropism. However, the picture is not complete with these two reasons alone. We need to include microbiota. Most tissues sites harbor a variety of unique bacteria, viruses and fungi, some such as our skin, GI tract, female reproductive tract abundantly so. Surely, our microbiota participate not only in every immune response that ensues in the tissue where they reside but perhaps also in maintaining that tissue's homeostasis, i.e. in immunoregulation? Thus, gut-, skin- or eye-associated CD4 T cell immune responses to the same antigen could be anticipated to be different and indeed are.So here's where we are. We immunologists identified Th1 and Th2 using a variety of highly artificial in vitro cell culture techniques, we observed some apparent evidence of this dichotomy in CD4 helper T cell function in vivo with the experimental mouse model of leishmaniasis, the early promise of this mouse model did not pan out along predicted lines, the mental construct imposed by this dichotomy nevertheless persisted and we began to classify an increasing plethora of CD4 T cell subsets such as Th3, Th9, Th17, Treg and Tfh over the past two decades. In other words, we let our increasing technological proficiency dictate the course for understanding the underlying biology rather than the other way around. Doing so, it took years before we came full circle to appreciating CD4 helper T cell plasticity (17), i.e. that CD4 helper T cells do not actually differentiate terminally into non-overlapping or mutually exclusive or even antagonistic secretion of particular groups of cytokines with different effector functions such as Th1, Th2, Th3, Th17, etc but rather they evolve particular overlapping features of functionalities depending on the activating cell(s), site(s) and microbiota, i.e. the CD4 T cell's environment. Coming full circle in this fashion? Now that's what I call irony.BibliographyThe World of Th1/Th2 Subsets: First ProofPillars Article: Two Types of Murine Helper T Cell Clone. I. Definition According to Profiles of Lymphokine Activities and Secreted Proteins. J. Immunol., 1986, 136: 2348-2357.Reciprocal expression of interferon gamma or interleukin 4 during the resolution or progression of murine leishmaniasis. Evidence for expansion of distinct helper T cell subsets.Page on uiowa.eduNoben-Trauth, Nancy, Pascale Kropf, and Ingrid Müller. "Susceptibility to Leishmania major infection in interleukin-4-deficient mice." Science 271.5251 (1996): 987-990.Page on nih.govInduction and mechanism of action of transforming growth factor-bet...Page on bjmu.edu.cnThe role of the CD28 receptor during T cell responses to antigen.Page on nih.govThe function role of GATA-3 in Th1 and Th2 differentiation.Kelso, Anne, et al. "Heterogeneity in lymphokine profiles of CD4+ and CD8+ T cells and clones activated in vivo and in vitro." Immunological reviews 123.1 (1991): 85-114Kelso, Anne. "Th1 and Th2 subsets: paradigms lost?." Immunology today 16.8 (1995): 374-379)Cytokine-secreting follicular T cells shape the antibody repertoireIL-4-producing CD4+ T cells in reactive lymph nodes during helminth infection are T follicular helper cellsMatzinger, Polly, and Tirumalai Kamala. "Tissue-based class control: the other side of tolerance." Nature Reviews Immunology 11.3 (2011): 221-230.Page on nih.govThanks for the A2A, Alex Rubinsteyn. Maybe you were seeking a few simple lines of answer. I give you instead an extremely brief history of the past three decades of CD4 helper T cell biology. Salut!

Railway Jobs 2019 for 10th Pass, 12th Pass, ITI, Diploma, Engineering Graduates, Degree, Post Graduate holders of Fresher and experienced candidates. The Railway Vacancy 2019 notification / vacancy sources gathered from Railway Recruitment Control Board (RRB), Railway Recruitment Cell (RRC) and Govt Officials.Indian Railway Jobs is one of the most prestigious government sector vacancies in India. Indian Citizens who looking for career opportunity in Ministry of Railways and Railway relegated central Govt jobs, get latest jobs opening list in Railway sector here. IndGovtJobs Website will listing latest and upcoming Railway Recruitment 2019 on every week. Every year, Indian Railways offering more than One lakh vacancies in various RRBs through Online application mode. Recent year, Railway Recruitment 2019 notification was available in digital format and also application should be registered through Online mode, Very rare Railway jobs 2019 notification has been called from offline prescribed format of application (Hard Copy) send to concerned Railway Boards.Railway Recruitment 2019 – Latest Railway Jobs 2019-20 Openings List: (Last updated on February 2019)Name of the Railway ZoneName of the PostsNo of VacanciesLast Date for ApplyDetails / Apply OnlineRailway Recruitment Boards (RRB)NTPC, Para Medical Staff, Ministerial and Isolated Categories and Level 1 Posts1,30,000+March / April 2019Full Details>>Mumbai Metro Rail Corporation Limited (MMRCL)Surveyor, Various Managers, Assistant, Engineer1218/03/2019Full Details>>Rail Wheel Factory BangaloreSports Quota 2018-191023/02/2019Full Details>>RITES LimitedJoint General Manager, Assistants, Hindi Assistants0827/02/2019Full Details>>Rail Coach Factory, KarpurthalaSports Quota 2018-190301/03/2019Full Details>>Northern RailwayCultural Quota0227/02/2019Full Details>>Kutch Railway Company Limited (KRC)Managing Director0114/03/2019Full Details>>Central RailwayCultural Quota0218/02/2019Full Details>>North Central RailwayCultural Quota (Vocational Light Classical, Keyboard Instrumental Music)0217/02/2019Full Details>>DFCCILSAP Consultants0513/02/2019Full Details>>South Western RailwaySports Quota 20190511/02/2019Full Details>>Maharashtra Metro Rail Corporation LimitedExperienced Engineers1612/02/2019Full Details>>Railway BoardDirector (Official Language)0111/02/2019Full Details>>Integral Coach Factory, ChennaiGraduate Apprentices, Diploma Apprentices22006/02/2019Full Details>>Bangalore Metro Rail Corporation Limited (BMRCL)Maintainer, Junior Engineer, Section Engineer17402/02/2019Full Details>>North Central RailwaySports Quota (SQ 2018-19)2106/02/2019Full Details>>West Central RailwayITI Apprentices1600Feb 2019Full Details>>West Central RailwayFitter, Welder, Electrician, Computer, Secretarial Assistants20027/01/2019Full Details>>Northern RailwayScouts and Guides Quota 2018-191930/01/2019Full Details>>South Western RailwayScouts and Guides Quota1128/01/2019Full Details>>South Western Railway (SWR) (RRC Hubli)Junior Technical Associates (JTA), Senior Technical Associates (STA)8101/02/2019Full Details>>Railway Recruitment Boards (RRB)Junior Engineer, Junior Engineer (IT), Depot Material Superintendent, Chemical and Metallurgical Assistant1384331/01/2019Full Details>>Northern RailwayApprentices109231/01/2019Full Details>>Railway Protection Force (RPF)Constable (Ancillary) Posts79830/01/2019Full Details>>North Central RailwayGroup C Posts against Sports Quota 2018-192128/01/2019Full Details>>North Central RailwayCultural Quota0228/01/2019Full Details>>Latest Government JobsGovt Jobs in Railway, Bank, PSU, Others100000+Feb 2019Govt Jobs >>Latest Engineer JobsVarious Engineering Posts2000+Feb 2019Engineer Jobs >>Recruitment against Quota: Sports Quota, Scouts & Guides Quota and Cultural Quota.Educational Qualifications: Minimum 10th class pass or ITI or equivalent trade for Group C & D Posts. Graduate / Post Graduate for Group A & B Posts.Railway Recruitment Posts: Gazetted (Group 'A' and 'B') and Non-Gazetted (Group 'C' and 'D') in 19 RRBs:-Group 'A' Posts –> Group A posts is carried out by UPSC - appointed through Civil Service Exam, Engineering Service Exam, and Combined Medical Service Examination.Group 'B' Posts –> This posts are not open to directly. The Group B posts link Section Officers Grade - upgraded posts from Group 'C' railway employees on deputation basis.Group 'C' Posts –> Technical and Non-Technical cadre posts like Clerk, Station Master, Ticket Collector, Commercial Apprentice, Traffic Apprentice, Engineering posts (Civil, Mechanical, Electrical, Signal & Telecommunication) etc.Group 'D' Posts –> These posts in various disciplines include Trackman, Helper, Assistant Points Man, Safaiwala / Safaiwali, Gunman, Peon etc.Other Posts –> ITI Apprentices, Sports Quota, Cultural Quota, Scouts and Guides Quota etc.Selection Procedure: Written Examination. There is no Interview (Viva Voce) after the written examination. For a very few specific (Group A & B) categories there is a Viva after the written exam, while for certain other categories there is a Skill Test (like typing test or stenography test) and for categories related to operational safety like Assistant Station Master, Assistant Loco Pilot, there will be an Aptitude Test.List of Indian Railway Recruitment Zones: Indian Railways organizational structure is divided into 17 zones, which are further sub-divided into various city wise divisions. All RRBs official website links and contact E-Mail List available at - http://www.rrcb.gov.in/rrbs.htmlRRB DivisionCityCentral Railway (CR)MumbaiEast Central Railway (ECR)BhubaneswarEastern Railway (ER)KolkataNorth Central Railway (NCR)AllahabadNorth Eastern Railway (NER)GorakhpurNorth Western Railway (NWR)JaipurNortheast Frontier Railway (NFR)GuwahatiNorthern Railway Railway (NR)DelhiSouth Central Railway (SCR)SecunderabadSouth East Central Railway (SECR)BilaspurSouth Eastern Railway (SER)KolkataSouth Western Railway (SWR)HubliSouthern Railway (SR)ChennaiWest Central Railway (WCR)JabalpurWestern Railway (WR)MumbaiMetro Railways List:Kolkata Metro Corporation Limited (KMRC)Delhi Metro Rail Corporation Limited (DMRC)Bangalore Metro Rail Corporation Limited (BMRC)Chennai Metro Rail Corporation Limited (CMRC)Mumbai Metro Rail Corporation Limited (MMRC)Kochi Metro Rail Corporation Limited (KMRC)Lucknow Metro Rail Corporation Limited (LMRC)Jaipur Metro Rail Corporation Limited (JMRCL)Nagpur Metro RailMetro Link Express for Gandhinagar and Ahmedabad (MEGA)Noida Metro Rail Corporation Limited (NMRCL)Hyderabad Metro Rail (HMRL)Navi Mumbai Metro (NMM)Rapid Metro, GurgaonRead more: Railway Recruitment 2019 - Railway Jobs (130036 Vacancies Opening) https://www.indgovtjobs.in/2013/09/railway-jobs-recruitment.html#ixzz5gGdyqiUR