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


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!

  • Regional Planner
    Introduction The Regulatory Submissions Planner will work within the Client organization, in the Regulatory Affairs Operations Regional department (Latin America [LA], Asia Pacific [AP], or Europe, Middle East and Africa [EMEA]). (more…)
    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…)
    Read More
  • Records Information Manager
    Function Create a planning entry and enter the registration details as applicable.Co-ordinate copying and dispatch (hard copy and electronical) of regulatory documents to Health Authorities and the Client's Affiliates world-wide in collaboration with regulatory product managers and concerned functions.Upon dispatch of the submission, archive submission.Proactively monitor Regulatory compliance.Ensure registration data is tracked and update the registration status details to align with submission information.Support data cleaning in close collaboration with the respective affiliates to ensure data quality.Act as a Subject Matter Expert (SME) for a specific activity on data management or dispatch.Support in any ad-hoc activities given by the immediate supervisor.Supports…
    Read More
  • 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…)
    Read More
  • Case Evaluator
    Function - Evaluation of SAE cases following the L2 path (all serious, legal, interventional studies, pregnancies) in accordance with regulatory requirements for AE reporting.- Determination of seriousness, drug product association and global labeling status (expected vs. unexpected) in order to assign the appropriate case reporting status for global distribution of regulatory case reports.- Addition of PSUR comments to individual case safety reports to facilitate PSUR authoring.- Execution of a high-quality, accurate and timely SAE case evaluation process within a therapeutic area and contribution to continuous improvement of PV system and processes.- Confirmation of the accuracy of medical coding of all…
    Read More
  • Polish speaker Customer Response Executive
    Introduction We are looking for Polish speaking candidates who will work on animal healthcare service desk support. (more…)
    Read More