Specialist RIM Data Maintenance, Dublin Pike

McDermott Laboratories Limited Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases.We have been included on number of award lists that demonstrate the impact we are making. Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas.We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment. For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience.The Role&What You Will Be Doing

Partner with the Regulatory teams on the creation/revision of records in the RIM system for a large, global portfolio of pharmaceutical products, including Application-level and Master Data level records. Collaborate with the Regulatory Affairs team to address queries related to the RIM system for field definitions, data entry standards, system workflows, dashboards, and searches.Participate in data cleansing operations to facilitate appropriate and timely access to data for key systems. Support the evaluation of data quality issues through review and analysis of system-generated consistency checks. Work with Regulatory colleagues to address items and help with bulk updates.Submit master data requests for dictionary updates to the RIM system. Propose improvements to the RIM system, processes, or procedures based on experience with its use. Contribute to the development and implementation of departmental Standard Operating Procedures (SOPs), user manuals, and data standards.About Your Skills&Experience

BS/BA in technology field, life sciences field, or other relevant discipline. Previous experience in pharmaceutical industry. Experience in Regulatory Affairs or Regulatory Operations is strongly preferred. Other pharmaceutical experience (e.g. Research&Development, Quality Assurance/Compliance) will be considered. Applicants whose past experience does not fully align with every requirement are encouraged to apply. Benefits

Competitive salaries, benefits and an inclusive environment. Career progression opportunities. Work-life balance initiatives. Viatis is an Equal Opportunity Employer. Viatis, a global healthcare company formed in 2020 through the combination of Mylan and Upjohn, a legacy division of Pfizer, aims to deliver increased access to affordable, quality medicines for patients worldwide, regardless of geography or circumstance, believing in healthcare as it should be– empowering people worldwide to live healthier at every stage of life.

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