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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!

  • Drug Safety Scientist
    Introduction Quality review of a single ICSR along with Data Entry support, Submission review, Reconciliiation activities and Support to EV Screening & Clinical Trial Protocol related activities. (more…)
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  • Case Processor
    Introduction Do you have analytical skills and a result-oriented mindset? Are you motivated to work in a multilingual environment where you can use your language skills on a daily basis? If your answer to both questions is yes, perfect! We have the best opportunity for you here in TATA Consultancy Services! (more…)
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  • 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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  • Patient Safety Administrator
    Introduction You will enter reports of drug side-effects from post-marketed or clinical study source to the safety database, and resolve queries related to pharmacy activities and individual case reports. (more…)
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