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Global Regulatory Affairs - Regulatory IT (all genders)

Your role:

As a Global Regulatory IT Expert you are responsible for the wide-ranging technical, strategic, and knowledge management of EHS activities as you evaluate and optimize the organizational design and (work) processes. Above all, your focus is to analyze and update the regulatory content in the system with regards to regulatory requirements.  Thus, you coordinate the regulatory requirements from the Global Registration Team and retrieve respective analyses and reports of regulatory master data for SAP EHS.  You support the Global Registration Team with your technical expertise with regards to development and support of IT applications (MS Access, SQL, Business Objects or other programming languages). As a Regulatory IT Expert in the Global Registration Team, you will be the first point of contact for the Digital Transformation Team being in the lead for EHS Master Data and for Merck IT for general data topics/solutions. In addition, you coordinate and perform the testing, evaluation and analysis of new functionalities together with the Digital Transformation Team, securing the continuous improvement of data and content support as well as efficient working procedures.


Who you are

  • Graduate degree in Natural Sciences (e.g. biologist, chemist), PhD preferable
  • Very good PC skills (e.g. Office, VBA, SQL, Python), IT -development\support experience
  • Min. 3 years of profound experience in the area of international Regulatory Affairs Management for chemicals programs
  • Excellent communication skills (very good command of English; German is an adavantage
  • Comfortable working in complex environments



Job Requisition ID:  187948
Location:  Darmstadt
Career Level:  D - Professional (4-9 years)
Working time model:  full-time

Job Segment: Medical, ERP, Environmental Health & Safety, Database, SQL, Healthcare, Technology

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