Tata Consultancy Services Tata Consultancy Services Facebook page Tata Consultancy Services Linkedin page Tata Consultancy Services YouTube page
Tata Consultancy Services Tata Tata Consultancy Services
Life Science

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!

  • Submission and Information Specialist
    Introduction Submission and Information Specialist will support formatting of documents and maintenance of these in document management systems as well as data entry activities into regulatory systems and publishing. (more…)
    REFERENCE NUMBER: #1145
    Read More
  • Regional Planner
    Introduction The Regulatory Submissions Planner will work within the MSD Global Regulatory Affairs and Clinical Safety (GRACS) organization, in the Regulatory Affairs Operations Regional department (Latin America [LA], Asia Pacific [AP], or Europe, Middle East and Africa [EMEA]). (more…)
    REFERENCE NUMBER: #1365
    Read More
  • 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 QA check for the published document. Will also be responsible for renewal and continuation of marketing licenses of the drug, Coordination with multiple stakeholders to report adverse events. (more…)
    REFERENCE NUMBER: #661
    Read More
  • 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…)
    REFERENCE NUMBER: #168
    Read More
  • 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…)
    REFERENCE NUMBER: #979
    Read More
  • 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…)
    REFERENCE NUMBER: #998
    Read More
  • English Speaker Customer Response Executive
    Introduction We are looking for English speaking candidates who will work on animal healthcare service desk support. (more…)
    REFERENCE NUMBER: #1111
    Read More
  • 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…
    REFERENCE NUMBER: #980
    Read More