摘要
Join us and become our next talent.
About the Role
Key Responsibilities:
· Leads the implementation of LC projects at SKU material level, ensuring on-time and compliant first deliveries.
· Creates, maintains and communicates a detailed Change Over Plan (COP) for LC projects regarding implementation dates, according to the overall strategic project/ program plan, in order to allow for early local Master Data set-up and planning at site and in countries.
· Works with a broad variety of stakeholders: Actively seek alignment with Project Lead and with the experts from different functions (e.g. project team members, CPO DRA, CPO demand planning, site tactical/ operational schedulers, Master Data Governance, other Supply Chain functions).
· Is responsible for the up-to-date assortment at SKU level of the assigned projects. Initiates the Material creation in absence of Master Data Steward and provides candidates and evaluation to clean obsolete SKU.
· Tracks regulatory approvals and trigger implementation of changes in the Change Control system in accordance to regulatory status and implementation strategy.
· Ensures compliance with GMP, regulatory requirements, HSE (including record management) and continuous improvement of quality relevant processes within area of responsibility.
· Plans and tracks changeover activities and project implementation milestones with all involved functions and proactively addresses/resolves or escalates potential issues through the Project Lead or project team members (e.g. incomplete Master Data causing missing demand).
· Ensures compliant shipment to customer for artwork changes approved only for packaging.
Essential Requirements:
• Minimum university degree in Natural sciences, Technical sciences or Economics.
• At least 2 years experience in various pharmaceutical functions e.g. supply chain / production and / or technical development.
• Active knowledge of English.
• Knowledge of Microsoft Office.
• Highly motivated, independent and self-initiative.
We offer temporary employment, with 6 months of probation period. Submit your application with the CV in Slovenian and English language.
You’ll receive:
Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, possibility to work from home, Pension scheme, Employee Recognition Scheme, Expanded program for the promotion of health in the field of physical, mental and social well-being (Wellbeing), employment at Top SI Employer, Unlimited learning and development opportunities.
Commitment to Diversity and Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
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For Slovenia:
Kot Ekspert upravljanja življenjske krivulje izdelka (m/ž/d) boste
Odgovorni za implementacijo projektov življenjskega cikla izdelka (LC), usklajevanje in koordinacija vseh deležnikov in funkcij, ki so vključeni v projekt življenjskega cikla. Zagotavljanje pravočasne in z zakonodajo ter standardi skladne implementacije projektov življenjskega cikla (lansiranje / spremembe / transferji / odprodaje oz. zmanjševanje dejavnosti) v skladu s projektnim načrtom in strategijo izvajanja ter ob upoštevanju zakonodaje, GMP standardov, SOP, ZVO, kodeksom ravnanja ter ostalimi internimi predpisi, dobrimi praksami in poslovnimi cilji.
Pridružite se nam in postanite naš naslednji talent!
Vaše ključne odgovornosti:
• Vodenje implementacije projektov življenskega cikla izdelka na materialnem nivoju (SKU), z namenom pravočasne in ustrezne prve dobave.
• Kreira, vzdržuje in komunicira podroben projektni plan sprememb in datumov implementacije (Change Over Plan - COP) v skladu s strategijo/planom projekta in tako omogoči pravočasno kreiranje lokalnih matičnih podatkov, planiranje aktivnosti na proizvodnih lokacijah in aktivnosti v državah.
• Sodeluje s številnimi udeleženimi deležniki in usklajuje aktivnosti s projektnim vodjem in strokovnjaki iz različnih funkcij (npr. člani projektne skupine, CPO DRA, planerji povpraševanj, taktičnimi / operativnimi planerji, skrbniki podatkov in z drugimi funkcijami v oskrbi) .
• Je odgovoren za posodobljen asortiman na materialni ravni (SKUs) dodeljenih projektov. Injicira ustvarjanje materiala v odsotnosti skrbnika matičnih podatkov in posreduje predloge in ocene za ukinitev zastarelih materialov (SKUs).
• Spremlja regulatorne odobrive sprememb in sproži izvajanje sprememb v sistemu za nadzor sprememb (Change Control System), v skladu z regulatornim statusom in strategijo izvajanja.
• Zagotavlja skladnost z GMP, regulatornimi zahtevami, ZVO (vključno z upravljanjem zapisov) in nenehno izboljševanje kakovosti procesov za svoje področje odgovornosti.
• Načrtuje in spremlja projektni plan sprememb (Change Over Plan) in izvedbo zastavljenih mejnikov projekta z vsemi vključenimi funkcijami in proaktivno obravnava / rešuje ali eskalira morebitne težave prek vodje projekta ali članov projektne skupine (npr. nepopolni matični podatki, ki se kažejo v manjkajočem povpraševanju (demands).
• Zagotavlja ustreznost odprem vezanih na pakiranje izdelka s spremembo v ovojnini /artworkih).
• Zastopanje vizije podjetja, vrednot in skrb za dobre medsebojne odnose s poslovnimi partnerji.
• Odgovornost za osebni in strokovni razvoj.
• lzvajanje in upoštevanje vseh navodil in zahtev za zagotavljanje varnega dela, varovanja okolja in premoženja.
• Ostale naloge določene z letnim pogovorom o ciljih in s kazalniki uspešnosti.
• Druge naloge po navodilu nadrejenega in naloge na podlagi posebnega imenovanja.
Vaš doprinos k delovnem mestu:
• Vsaj visokošolska stopnja izobrazbe naravoslovnotehnične ali ekonomskodružboslovne smeri.
• Minimalno 2 leta izkušenj na različnih funkcijah v farmaciji, npr.oskrba/proizvodnja in/ali tehnični razvoj.
• Aktivno znanje angleškega jezika.
• Poznavanje orodja Microsoft Office.
• Visoka motiviranost za delo, samostojnost in samoinciativnost.
Z izbranim kandidatom bomo sklenili delovno razmerje za določen čas s poskusno dobo 6 mesecev. Prijavo oddajte z življenjepisom v slovenskem in angleškem jeziku.
Kaj nudimo:
Konkurenčen plačni paket, letni bonus, fleksibilen način dela, z možnostjo prilagajanja urnika in delom od doma, zaposlitev v podjetju s certifikatom TOP Employer, pokojninsko shemo, shemo nagrajevanja in priznanja dosežkov, razširjeni program promocije zdravja na področju telesnega, duševnega in družbenega počutja (Polni življenja) ter dogodke, neomejene priložnosti za učenje in razvoj.
Predani smo raznolikosti in vključenosti
Novartis si prizadeva ustvariti izjemno, vključujoče delovno okolje in oblikovanje raznolikih timov, saj ti predstavljajo naše bolnike in skupnosti, ki jih oskrbujemo.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
Accessibility and accommodation
Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
