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Master data associate

Latina
Johnson & Johnson MedTech
Pubblicato il 11 settembre
Descrizione

Ph3About Innovative Medicine /h3 pOur 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. /p h3Position /h3 pWe are searching for the best talent for Master Data Associate to be in Borgo San Michele – Latina. For the Italian Production Plant of Johnson Johnson Innovative Medicine (Borgo San Michele - Latina) we are looking for a Master Data Associate to be hired on 12 months fixed term contract in the Data Readiness Department. The Master Data Associate will increase the strategic vision of the Data Readiness organization and execute base business activities related to SKU conversions, enabling the Latina site to Launch Growth by focusing on creation of new Launch SKUs and conversion of existing SKUs. You will be part of the Master Data team and report to the Data Readiness Lead. /p h3As a Master Data Associate, You Will /h3 ul liExecute base business activities respecting the procedures /li liGuarantee steps execution in pipeline according to the planning date /li liEnsure respect, quality and compliance of the activities of whom they will be responsible /li liManage the Data Readiness procedures according to quality and operative flows /li liCollaborate with the stakeholders in terms of increasing productivity/readiness of the base business in master data department /li liEscalate issue according performance management (daily/weekly/monthly) /li liManage quality issues relative the Data Readiness activities /li /ul h3Qualifications / Requirements /h3 ul liMaster’s degree in engineering, Pharmacy, Chemistry or Economics is preferred /li liGood knowledge of material master / check list manager / SAP /li liGood knowledge of quality, compliance and GMP related to manufacturing and packaging of pharmaceutical products /li liGood knowledge of planning process (Master production schedule, Detailed schedule, Budget calculation) is preferred /li liAbility to work in a cross functional team to ensure the correct execution of the activities according to the agreed timing and quality /li liSkills of ownership and accountability /li liSkilled in problem-solving and decision making /li liExperience in similar role is preferred /li liGood knowledge of English language (B2 level and above) /li /ul h3What to Expect /h3 ul liApplication review: We’ll carefully review your CV to see how your skills and experience align with the role. /li liGetting to know you: If there’s a good match, you’ll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have. /li liStaying informed: We will keep you updated and explain what to expect at each step. /li liFinal steps: For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide you through these. /li /ul pAt Johnson Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time. /p pFinally, at the end of the process, we’ll invite you to share feedback in a short survey — your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson Johnson. We’re excited to learn more about you and wish you the best of luck in the process! /p /p #J-18808-Ljbffr

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