Regulatory Affairs Professional, Data Integrity Emea

Johnson & Johnson Johnson & Johnson · Pharma · Warsaw, Masovian, Poland +1

This role focuses on managing and ensuring the integrity of regulatory data within EMEA for Johnson & Johnson's Innovative Medicine division. Responsibilities include updating regulatory tracking systems, scrutinizing data entry requests, and collaborating with data owners to maintain accurate and compliant regulatory information. The role also supports audits, process improvements, and provides guidance on data maintenance.

What you'd actually do

  1. Update the regulatory tracking system (i.e. InSight) and/or the labeling information tracking system (i.e. LIFT) based on data entry requests received from Data Owners (e.g. EMEA Local Operating Companies [LOC], Cross-Regional Operations & Strategic Support teams (C-ROSS), EMEA Regulatory Affairs Therapeutic Areas) for a variety of regulatory procedures, including but not limited to: Marketing Authorisation Applications, License Renewals, Labeling variations, Chemistry Manufacturing and Controls (CMC) variations, License Withdrawals/Transfers/Expiries
  2. Scrutinize data entry requests with Data Owners and instruct Data Onwers as needed, to ensure consistency and quality of data entered in InSight and LIFT.
  3. Follow-up with Data Owners to ensure completion of the assigned data entry request.
  4. Maintain a good understanding of all Regulatory procedures and the corresponding Internal Global Job Aids and Procedural documents to ensure that requested data are timely and accurately entered in the applicable regulatory systems.
  5. Collaborate effectively with the Data Owners and ensure data owner alignment with data entered on their behalf.

Skills

Required

  • At least 2 years of Regulatory Affairs experience
  • Good understanding of Marketing Authorisation data and regulatory procedures (National as well as EU procedures)
  • Experience with regulatory data planning, tracking (including regulatory data verification), remediation, and data quality support
  • Experience with EU XEVMPD and familiarity with the EMA Eudravigilance data environment
  • Knowledge of compliance requirements and advanced process thinking
  • Ability to link legal and company internal requirements with regulatory process aspects and the applicable task management
  • Proven ability to monitor multiple actions and timelines and follow up until completion
  • Experience in working with limited supervision and able to make independent decisions
  • Ability to work effectively in a matrix organisation with multiple cross-functional stakeholders on global, regional and local level
  • Excellent cross-cultural communication skills in English

Nice to have

  • A minimum of a university degree or equivalent by experience
  • Good technical skills
  • Proactive team-player, able to take charge and follow-through

What the JD emphasized

  • Data Integrity
  • regulatory data