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Regulatory Team Leader

Állás részletei

  • Cég neve

    Cognizant

  • Munkavégzés helye

    Hibrid Mill Park - Budapest, Épület, MillPark Centre, Soroksári út 44 A-2nd Floor, 1095
  • Fizetés

    Bónusz
  • Egyéb juttatások

    • Szakmai tréningek
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  • Munkaidő, foglalkoztatás jellege

    • Teljes munkaidő
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Állás leírása

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Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build, and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant (a member of the NASDAQ-100 and one of Forbes World’s Best Employers 2025) is consistently listed among the most admired companies in the world.

The position exists to participate in the regulatory program of our pharmaceutical partner, being part of a global team and leading a team which is part of it.

 

  • 40 hours per week
  • Normal business hours
  • Office attendance: Once a week

 

Tasks and Responsibilities

  • Tracking different regulatory submissions in the corporate regulatory database – update database with specific documents and/or information
  • Running daily queries, providing reports to client stakeholders
  • Applying technical knowledge to perform quality check on the entries
  • Ensuring compliance with KPIs
  • Optimizing utilization and effective resource allocation planning for the team
  • 100% compliance for work allocation
  • Good team management (indicated through no major escalations)
  • Ensure adherence to Cognizant and Client SOPs (Standard Operating Procedure) or internal standards and processes
  • Responsible for regular FMEA update and CAPA management
  • Managing BCP and operations
  • Effective risk management and issue handling by conducting daily huddle and escalating them on time
  • Communicating with client representative, understanding client expectations
  • Establishing and developing processes and procedures in the team
  • Complete all mandatory training courses as applicable
  • Communicating issues to Delivery Site Lead
  • Education: Bachelor’s degree in Life Sciences or Pharmacy
  • Experience:
    • 2–5 years of professional experience in Regulatory Affairs
    • Hands-on experience in Pharmacovigilance (PV) data handling
  • Skills:
    • Strong attention to detail and accuracy in documentation
    • Good understanding of regulatory guidelines and compliance standards
    • Proficiency in data management tools and MS Office applications
  • Language: Excellent written and spoken English (additional languages are a plus)
  • Competitive salary and cafeteria benefits; All You Can Move SportPass (at a discounted price), annual bonus, medical benefits, and other perks
  • Risk and accident insurance
  • Chance to be part of a rapidly expanding organization
  • Training and continuous learning and certification opportunities
  • Multilingual environment, native colleagues
  • Pleasant and inspiring working atmosphere with multicultural community and state-of-the-art technologies
  • Easy-to-access location and modern office building (easy to reach from city center, 10–15 minute commute)
  • Reimbursable language courses

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