Work Your Magic with us Ready to explore break barriers and discover more We know you ve got big plans - so do we Our colleagues across the globe love innovating with science and technology to enrich people s lives with our solutions in Healthcare Life Science and Electronics Together we dream big and are passionate about caring for our rich mix of people customers patients and planet That s why we are always looking for curious minds that see themselves imagining the unimageable with us Your Role Labeling Compliance Operations Safety Variation Compliance Monitoring Presentation of Compliance results to the GRA Governance team Quarterly Safety variation KPI provision and presentation of safety variation compliance in GPS Compliance Review Board chaired by the EU QPPV QC Finalization and Delivery of PSMF Annex F2 3 A B and C sub-annexes to the GPS Providing Inputs for Labeling Process Automation Supporting PV and Labeling Audits and Inspections worldwide Driving process improvement initiatives e g Veeva Breeze process optimization Creation and Update of Labeling Quality Documents Oversight of labeling Content Deviation and Artwork initiation compliance Check process May also be required to support Labeling Strategy at peak times as overall workload allows Labeling Product Lead for marketed product portfolio Creates updates and oversees implementation of Core labeling Documents Coordinates Labeling Team discussion on key labeling topics Provides labeling inputs for HA queries and PBRERs Responsible for update and maintenance of MRP DCP and CP product information Cooperation Interfaces with other Departments Functions Internally Global Regulatory Affairs Global Healthcare Operations Global Regulatory Operations Global Patient Safety and EU QPPV office and IT teams Externally External Interfaces Veeva and other IT vendors Label Net Forums Who You are Education MSc in Pharmaceutical Sciences or related discipline Work Experience 7-10 years of overall experience in Labeling Strategy and Operations Attention to detail excellent time management project management presentation and communication skills written or oral significant experience with VEEVA system and IT tools often used in regulatory departments in the pharmaceutical industry Valuable understanding of Global Labeling Compliance topics as well as various operational activities in global labeling departments of regulatory affairs What we offer We are curious minds that come from a broad range of backgrounds perspectives and life experiences We celebrate all dimensions of diversity and believe that it drives excellence and innovation strengthening our ability to lead in science and technology We are committed to creating access and opportunities for all to develop and grow at your own pace Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress Apply now and become a part of our diverse team