RA Professional ERMC Artwork Mgmt

hace 1 semana


Madrid, España Johnson & Johnson Innovative Medicine A tiempo completo

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Learn more Job Function Regulatory Affairs Group Job Sub Function Regulatory Product Submissions and Registration Job Category Professional Locations Lisbon, Portugal; Madrid, Spain; Novi Beograd, Beograd, Serbia; Warsaw, Masovian, Poland About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more Job Description We are searching for the best talent for a RA Professional ERMC Artwork Management to be in Warsaw, Poland; Madrid, Spain; Lisbon, Portugal, or Belgrade, Serbia. Responsibilities Use of Artwork management System to initiate artwork for new labelling or changes to current labelling into production and/or generation of mock-up needed for regulatory submissions Complete review of the artwork (using electronic tool, where possible) and co‑ordinate the final approval of the artwork with Local Operating Companies driven by the agreed deadlines Entering data and using tools to monitor metrics for tracking of implementation of packaging material Liaise with Local Operating Companies Regulatory Affairs, quality, Product Artwork, supply chain, packaging sites internal/external to meet both Health Authorities implementation timelines and minimize current stock /component write‑off costs Performing and/or co‑ordination of Quality Check (QC) of local Product Information Communication with local stakeholders of the Local Operating Companies in scope during the review process Requirements Previous experience of 2 years in Regulatory Affairs and artwork management Experience of working in a virtual team and/or global organization would be an asset Experience in working with limited supervision and able to make independent decisions is of advantage Cultural sensitivity and ability to work and thrive in a multi‑cultural environment Experience with computer systems usage (MS office, excel) Proficient level of English Knowledge of multiple languages would be an asset Accuracy, precision and respect of timelines is mandatory Employment Type Full‑time #J-18808-Ljbffr



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