会社名
非公開 No,RE181104
企業タイプ
外資系企業
職種
医薬品:製造・生産管理・QC・QA
仕事内容
1) Cross-site planning
• Prepare analysis of distributed supply requirements for cross-site discussion; Drive cross-site calls, flagging shortage risks and agree any plan updates
• Monitor bulk/API requirements based on PoR; Adjust buffers to ensure production plan feasibility; ID and communicate risks
2) Supply prioritization
• Review high-level supply requirements across full PP/DS horizon; Prioritize orders based on market inventory position, SKU segmentation, and site/above site production strategy; Firm orders at week 11 (Pack) / at week 13 (for weeks 13-16 for DP)
3) Volume projection and PoR
• Collaborate with Site Planning Team to resolve asset balancing trade-offs ensuring sufficient supply performance; Publish site PoR
• Prepare rough cut capacity projections for assigned resources; aggregate capacity constrained and balanced PoR for network review of capacity issues
4) Demand validation
• Monitor month-on-month demand changes over a rolling 3-12 month horizon; Flag substantial changes in demand
• Liaise with markets and FG sites to interrogate and validate demand changes; ID root causes; Ensure system requirements up to date
5) Demand planning
• Model system demand gaps caused by source change / product change working with PNS and leveraging system tools (e.g. LIE)
• Incorporate demand for new products changes into the plan
6) Demand signal maintenance
• Use cross-site call forum to flag demand signal issues; Establish root-cause (MD vs. process)
• Work with network stakeholders to resolve demand signal issues; Track adherence
7) Demand and supply alert management
• Review alerts (exceeding threshold); ID proposed changes; Write system notes to prioritize orders within 10 weeks (Pack) / 12 weeks (DP); Share urgent issues with Site Planner
• ID bulk/API supply issues and proposed plan changes; Write system notes; Communicate urgent issues
8) Allocation planning
• Develop a bulk allocation plan with BSL guidance and handover to Site Planner (in constrained supply scenarios)
9) Supply governance
• Participate in weekly supply governance calls to troubleshoot low stock issues and balance cost vs. supply trade-offs
• Track root causes and prioritize remediation and prevention actions
10) System parameterization
• Review / update system parameters (SS, MOQ / Lot Size, Shelflife) to optimize cost / supply trade-offs and SCAs; Review MD workflow; work with MD team to define and set system parameters in system as required
11) Inventory control (Bulk/API)
• Track, review and communicate bulk/API inventory vs. target MoH
• Monitor bulk/API shelf life; Ensure adherence to RIDS avoidance processes; Coordinate RIDS process with site MRB
12) BSL/PPL liaison
• Serve as point-of-contact for brand- and site-related queries from above-site
対象条件
・Strong experience and knowledge of supply chain management and production planning in pharmaceutical environment, direct production planning experience is preferable
・High capability of system skill sets with deep SAP knowledge, especially APO SNP and PPDS. Computer literacy and analytical skills
・ Global communication skills with business-level fluency in written and spoken English(TOEIC 730), and pro-active problem solving behavior and motivation for self-improvement
年齢
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勤務地
東京/名古屋

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