Description:The Johnson & Johnson Family of CompaniesA global leader in health and personal care, with over 125,000 employees in over 275 companies in 60 countries. We work with healthcare partners to touch the lives of more than a billion people every day worldwide.“By caring, one person at a time, we aspire to help billions of people live longer, healthier, happier lives.”Johnson & Johnson Innovative Medicine is recruiting for an EMEA RMC Artwork Management Associate. You will work in an international team spread around EMEA. This role will be operating in a hybrid office/home model. Possible locations are Algeria, Egypt, Poland, Lebanon, Italy, and Greece.As an Artwork Management Professional, you will coordinate all the artwork-related activities in the region and ensure that our artwork fits local health authorities and EMA requirements. You will be working closely with other departments, gaining valuable experience and insights into a global healthcare company.EMEA RMC Artwork Management The Regulatory Management Center is a new regional organization to handle most of the Local Operating Companies activities led by senior regional regulatory staff, where they will handle tactical Life Cycle Management processes (CMC Variations and Labeling Changes) in the region. The Center will be embedded in the EMEA region and will work closely with the respective Local Operating Companies and regional and global departments.Responsibilities:Use of Artwork management System to initiate artwork for new labeling or changes to current labeling into production and/or generation of mock-up needed for regulatory submissionsComplete review of the artwork (using an 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 materialLiaise 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 costsPerforming and/or co-ordination of Quality Check (QC) of local Product InformationCommunication with partners of the Local Operating Companies in scope during the review processQualifications:Requirements:Previous experience of 2 years in Regulatory Affairs and artwork managementExperience of working in a virtual team and/or global organization would be an assetExperience in working with limited supervision and able to make independent decisions is of advantageCultural sensitivity and ability to work and thrive in a multi-cultural environmentExperience with computer systems usage (MS Office, excel)Proficient level of EnglishKnowledge of multiple languages would be an assetAccuracy, precision, and respect for timelines are mandatoryJohnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against based on disability.For more information on how we support the whole health of our employees throughout their wellness, career, and life journey, please visit www.careers.jnj.com.We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment. Please contact us to request an accommodation