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Life Science


At TCS in the Life Sciences and Health Care area we deal with pharmacovigilance and publishing activities for global pharmaceutical companies, TCS` customers. We serve patient safety with the core purpose to add value to our client’s products and safeguard the success of the business by focusing on protection of patients. We ensure that all relevant information concerning the safety of the client’s products is collected, evaluated and communicated. Our teams ensure timely and efficient reporting of adverse events and other information from pertinent to the safety profile of products towards regulatory authorities around the world as well it is essential that we comply with current regulations and guidelines. We are involved in publishing activities that is mostly connected to regulatory part of the pharmaceutical industry – but also makes sure that our customers` drugs can be used safely all over the word. Our team takes active and important parts in our clients’ everyday life and production – the business results show that they trust our knowledge and expertise.


Search for our job opportunities below and choose your own path!

  • Junior Publishing Specialist
    Introduction Publishing Associate will support authors to publish submission ready documents by applying appropriate compliance check to the type of document, publishing the document & also performing the QC check for the published documents. Associate will also be responsible for renewals, continuation of marketing licenses of the drug and coordination with multiple stakeholders to report adverse events. (more…)
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  • English Speaker Customer Response Executive
    Introduction We are looking for English speaking candidates who will work on animal healthcare service desk support. (more…)
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  • Senior Publishing Specialist
    Function 1. Primary Responsibilities Support and provide coordination, compilation and publishing expertise in the preparation of new and existing regulatory applications including initial applications (CTAs, MAAs etc.), amendments, supplements, variations and other submissions in compliance with health authority regulationsPrimary focus is on regulatory submissions of moderate to high complexity both eCTD and non-eCTD format, including all Modules accountability for large submissions without supervisionRegularly represent PDRO at RAFT by providing regulatory and technical input and contributing in project planning; Update PDRO on changes of strategies, timelines and risk assessment 2. Submission coordination and publishing tasks Lead and coordinate the compilation of…
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  • Print and Dispatch Coordinator
    Introduction The Print and Dispatch Coordinator (PDC) will be involved in following activities: Preparation and collation of the final submission output for onward transmission in Paper or hard copy or electronic format as applicable to country specific requirements. PDC will support Submission Manager to print dossiers, burn CDs/DVDs, submit electronic output via portal/gateway and co-ordinate dispatch using the Sponsor’s standard operating procedures and Country specific regulatory requirements.PDC is also responsible for requesting CPPs from MPA, Sweden; MHRA, UK; and EMA PDC is also responsible for the scanning of market specific documentation for inclusion by the DMS into relevant Sponsor’s system.…
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  • Polish speaker Customer Response Executive
    Introduction We are looking for Polish speaking candidates who will work on animal healthcare service desk support. (more…)
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