Manage system performance, troubleshoot issues, and coordinate upgrades with IT and vendors.
Collaborate with cross-functional teams (RA, Quality, IT) to streamline regulatory workflows and improve system usability.
Train users and support audits by ensuring timely access to regulatory documentation.
Lead digital transformation initiatives and identify automation opportunities that can develop into projects.
Develop project plans, manage stakeholders, change management, and ensure smooth transition.
Manage the creation, governance, and quality of product registration and regulatory master data.
Ensure data accuracy, consistency, and compliance with global submission standards.
Lead cross-functional data initiatives and support data stewards with validation and guidance.

Degree in Life Sciences, Data Science, or IT
5+ years’ experience in the regulatory field, preferably with experience in data and/or system management
Experience with Veeva or similar RIM/Regulatory systems
Excellent communication and problem-solving skills
Excellent analytical skills
ability to analyze and interpret complex regulatory and scientific data
Fluency in English and Hungarian
Proven track record in leading projects

Senior Product Information Manager

Key skills