Genentech-posted 3 months ago
$139,300 - $258,700/Yr
Full-time
South San Francisco, CA
Chemical Manufacturing

As a Clinical Network Planner, you will be responsible for the oversight of the aggregate Drug Substance, Drug Product, and/or Finished Good demand and supply plans (initial & resupply) within the mid to long term horizon (months 3 up to 36) across the overall network. You will partner with Molecule/Study Planner and Long Range Planner to ensure alignment between mid & long term plans. Your previous clinical supply chain expertise, combined with an in-depth understanding of systems and processes as well as state-of-the-art knowledge of data science methodologies provide a sound basis to drive decision making across all clinical assets and influencing of our stakeholders across all levels of the organization. You consolidate, manage and analyze network wide demand, supply and capacity scenario analysis across the different clinical technologies, drive necessary trade-off evaluation for production at a portfolio level within a site and network level with appropriate stakeholders. Assess feasibility of plan by managing high priority demand requirements and workflow. Communicate and escalate plan and risks as appropriate through the CD&OP process. Own escalations and drive solutions at the appropriate organizational level. Evaluate capabilities of current clinical supply chain assets to ensure alignment with future customer and Pharma portfolio requirements. Partner with key stakeholders across Clinical Supply to ensure the effectiveness of CD&OP processes. Manage sourcing processes to determine strategic decisions and guidance regarding internal manufacturing versus outsourcing to contract manufacturing organizations: drive strategic sourcing assessments and key decisions to Clinical Demand & Operations Planning (CD&OP), key stakeholders, and senior management. Review performance metrics to drive improvement via CD&OP process in partnership with Clinical Supply Planning leadership (i.e. stock-outs, order change requests, inventory, and forecast). Lead cross-functional process improvement teams as appropriate to coordinate with SMEs within the organization to generate KPIs and metrics, maintain and improve performance metrics and process.

  • Oversee aggregate Drug Substance, Drug Product, and/or Finished Good demand and supply plans.
  • Partner with Molecule/Study Planner and Long Range Planner for alignment of plans.
  • Consolidate, manage, and analyze network-wide demand, supply, and capacity scenario analysis.
  • Drive trade-off evaluations for production at portfolio and site levels.
  • Assess feasibility of plans by managing high priority demand requirements.
  • Communicate and escalate plans and risks through the CD&OP process.
  • Evaluate capabilities of current clinical supply chain assets.
  • Manage sourcing processes for strategic decisions regarding manufacturing.
  • Review performance metrics to drive improvements.
  • Lead cross-functional process improvement teams.
  • 10+ years of Supply Chain experience, primarily in the pharmaceutical industry.
  • Minimum of 3 years in Clinical Supply Chain.
  • Detailed knowledge of Clinical Development and exposure to Technical Development Teams.
  • In-depth knowledge of Clinical Supply Chain Planning.
  • Solid understanding of drug development processes and clinical trial design.
  • Strong analytical, logic, and problem-solving skills.
  • Advanced ERP system experience, preferably SAP/4S HANA and OMP.
  • Excellent verbal/written communication and presentation skills.
  • Ability to lead ad hoc teams and perform work without supervision.
  • Academic degree in supply chain management or life sciences.
  • Further education in Digital and AI strategy, e.g., Master's Degree in AI.
  • Discretionary annual bonus based on individual and Company performance.
  • Equal opportunity employer policies.
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