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 unimaginable with us United As One for Patients our purpose in Healthcare is to help create improve and prolong lives We develop medicines intelligent devices and innovative technologies in therapeutic areas such as Oncology Neurology and Fertility Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life Joining our Healthcare team is becoming part of a diverse inclusive and flexible working culture presenting great opportunities for personal development and career advancement across the globe Your Role You are an experienced skilled with a strong background in Regulatory Affairs dedicated to enhancing data quality and compliance within the pharmaceutical industry You possess a solid understanding of regulatory processes and are adept at managing teams to support the regulatory lifecycle Who You Are Minimum Requirements Experience At least 8 years of professional experience in the pharmaceutical service provider or IT industry with a minimum of 6 years in Regulatory Affairs Education Basic degree in a scientific discipline or related work experience in the chemical-pharmaceutical industry Maximum Requirements Manage the Regulatory Information Management RIM team to support regulatory lifecycle management Lead Regulatory Data Quality initiatives and ensure compliance across VEEVA Vault and related systems Conduct regular assessments of data quality metrics ensuring adherence to established standards Identify root causes of issues related to processes systems or personnel Drive data cleansing activities and implement innovative technology solutions to enhance regulatory processes including automation and AI projects Collaborate with Global Regulatory Affairs and cross-functional teams to improve data quality and process efficiency Promote data literacy and Data Governance among stakeholders Ensure compliance with health authority data submission requirements maintaining consistency across all submissions Communicate effectively with stakeholders to support regulatory objectives Ensure regulatory data accuracy completeness and compliance with global standards e g IDMP xEVMPD What we offer We are curious minds that come from a broad range of backgrounds perspectives and life experiences We believe that this variety 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 a team that is dedicated to Sparking Discovery and Elevating Humanity

📌 Expert -regulatory Information And Data Quality (Karnataka)
🏢 Merck
📍 Karnataka