Job Description

Summary Drive and execute labelling activities for clinical trial supplies (IMP) to ensure fulfillment of supply chain. Resulting in no stock outs /missed milestones and/or supply interruptions impacting patients due to label quality or availability.
Has operational end-to-end responsibility for assigned supply activity (label related). Leads and man-ages activities and participates in cross-functional teams.Your responsibilities will include, but are not limited to:\xc2\xb7Is responsible for generation/coordination of labels for IMP, medication list/randomization list/randomization schedules and ensures agreed landmarks, quality and costs are met. Is accountable for label compliance with respect to study design, pack design, pack material, analytical specifications of the IMP along with country specific regulatory requirements and Novartis standards of compliance.\xc2\xb7If nominated leads overall governance and/or maintains Phrase Library (validated repository of country specific regulatory requirement and translations of phrases in country specific languages). If nominated be a system owner for Systems managed by CLM team and lead/co-lead system enhancement initiatives as appropriate.\xc2\xb7If nominated be a qualified GMP line unit checker for label(s), as defined in SOP, drive culture of quality within the team. Leads investigations if certified in case of quality events/deviations or any non-Right First Time(RFT) cases when required.\xc2\xb7Keeps clear alignment with all the internal (e.g. Clinical Trial Supply Managers, Supply Chain Managers etc.) and external (e.g. external label service providers for specialized labels) partners for IMP label related activities. Is responsible for communicating challenges to internal and external customers and bring solutions to mitigate any risk(s). Leads as a subject matter expert/functional guide on label process during internal/external inspections.\xc2\xb7Is responsible for communicating challenges to internal and external partners and bring solutions to mitigate any risks on project level. Adapts priorities in response to changing needs. Knows when to act independently or when to call out issues. Support the Business owner by coordinating the vendor management and vendor performance.\xc2\xb7Manages all applicable finance activities, including grants, purchase orders (PO) and invoice approval for IMP labels, as applicable. Works closely with BPO (Business Process Owner) to define processes, identify and support initiatives for process improvement and simplification, deliver key functional objective(s) along with high quality standards and operational excellence when required.\xc2\xb7Be a mentor for the new CLM associates if nominated. Ensures colleagues know and use the appropriate processes and procedures and are aware of the risks of non-compliance. Supports Business Process Owner (BPO) to assess risks related to CLM and have robust process in place. Actively participates in projects, networks and/or forums. Acts as a role model for Novartis values and behaviors.\xc2\xb7
5 years of practical experience in chemical / pharmaceutical industry or
3 years of experience in field of expertise\xc2\xb7Good knowledge about the Drug Development and clinical supply process\xc2\xb7Basic project management, good organization and planning skills\xc2\xb7Knowledge of relevant regulations (e.g. GMP, HSE etc.) and Novartis specific standards.\xc2\xb7Demonstrates problem-solving and idea generation skills\xc2\xb7Good presentation skills; Fundamental Leadership skills.\xc2\xb7Very good communication, negotiation and interpersonal skills. Ability to work in interdisciplinary teams..Why Novartis?Our purpose is to reimagine medicine to improve and extend people\xe2\x80\x99s lives and our vision is to become the most valued and trusted medicines company in the world. How can weachieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here:Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here:Skills Desired Continual Improvement Process, Master Data, Materials Management, Materials Requirements Planning (MRP), Production Planning, Project Management, Supply Chain Management (SCM), Supply Chain Planning (SCP), Warehouse Management System (WMS)

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