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Senior Product Information Manager
Gedeon Richter Pharma GmbHHungaryfull_timeVerifiedPosted 13 Oct 2025
About the role
<p><span><span> Join the professional team of the 120-year-old Gedeon Richter Plc., a leading pharmaceutical company in Hungary and the region!</span></span></p>
<p><span><span>We do not base our success on the great deeds of lonely heroes. At Richter, we believe in active co-operation - within and outside the teams. We know how to collaborate effectively and respectfully with professionals of different fields, disciplines, and organisational units.</span></span></p>
<p><span><span>Gedeon Richter is looking for a committed and experienced professional for the position</span></span></p>
<p><span><span><b><b>Senior Product Information Manager</b></b></span></span></p>
<h2><b>About the role</b></h2>
<p><span>We’re seeking a strategic and detail-oriented <strong>Senior Product Information Manager</strong> to lead regulatory data initiatives, take part in maintain our Regulatory Information Management System (RIMS), and drive technology transformation projects. This role is central to ensuring data integrity, regulatory operation performance efficiency, and regulatory compliance across global markets.</span></p><h2><b>Key Responsibilities</b></h2>
<p><span><strong>Regulatory Data Management</strong></span></p>
<ul>
<li><span>Manage the creation, governance, and quality of product registration and regulatory master data</span></li>
<li><span>Ensure data accuracy, consistency, and compliance with global submission standards</span></li>
<li><span>Lead cross-functional data initiatives and support data stewards with validation and guidance</span></li>
</ul>
<p><span><strong>RIMS Maintenance</strong></span></p>
<ul>
<li><span>Manage system performance, troubleshoot issues, and coordinate upgrades with IT and vendors</span></li>
<li><span>Collaborate with cross-functional teams (RA, Quality, IT) to streamline regulatory workflows and improve system usability</span></li>
<li><span>Train users and support audits by ensuring timely access to regulatory documentation</span></li>
</ul>
<p><span><strong>Technology Transformation Projects</strong></span></p>
<ul>
<li><span>Lead digital transformation initiatives</span></li>
<li><span>Identify automation opportunities that can develop into projects</span></li>
<li><span>Develop project plans, manage stakeholders, change management, and ensure smooth transition</span></li>
</ul><h2><b>Your profile</b></h2>
<ul>
<li><span>Degree in Life Sciences, Data Science, or IT</span></li>
<li><span>5+ years’ experience in the regulatory field, preferably with experience in data and/or system management</span></li>
<li><span>Experience with Veeva or similar RIM/Regulatory systems</span></li>
<li><span>Proven track record in leading projects</span></li>
<li><span>Strong analytical, communication, and stakeholder management skills.</span></li>
</ul><h2><b>We offer</b></h2>
<ul>
<li>Great opportunity for professional development in an innovation driven department</li>
<li>Great reputation at a well established pharmaceutical firm</li>
<li>Stability and a trustworthy workplace</li>
<li>Work in multidisciplinary teams</li>
<li>Training and development opportunities</li>
<li>Medical services and life insurance</li>
<li>Various sport and health opportunities</li>
<li>Excellent work life balance</li>
</ul><p><span><span>The Richter community is looking forward to your application.</span></span></p>
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