Specialist (m/f/d) New Product Introduction

vor 1 Woche

Rothenburg, Schweiz NES Global Deutschland GmbH NES Fircroft Vollzeit

We have an exciting opportunity for a New Product Introduction Specialist (m/f/d) in Switzerland

Tasks
  • Leading cross-functional teams, managing complex information flow, coordinating, and integrating the functional/tactical project management activities for New Product Introduction, in close collaboration with Value Chain Management, Global Launch Planning, and partner with E2E Planners, other Supply Chain functions, and stakeholders across divisions (GHH & MRL).
  • Coordinate activities to mitigate risks related to the different milestones across the New Product Introduction stages including, but not limited to: PLR Approval, Code Creation, Initial RCT update, Forecast Positioning, Artwork Readiness, First Packaging, in line with the Health Authority Approval to guarantee successful launches by ensuring system readiness to allow MMD execution.
  • Coordinate activities to mitigate risks related to Artwork Readiness. Liaise with Regulatory Affairs, Artwork Centers, and Quality for timely execution
  • Track, and report KPIs mitigating risks to minimize impact on business; participate and provide input to the IBP process (Demand Reviews, Site Supply Reviews).
  • Understand & translate the packaging lead times, capacity issues, process reliability issues, sourcing flows, market specific requirements (e.g. TOI, shelf life requirements, etc.) and regulatory issues impacting supply into appropriate risk mitigation actions
  • Work closely with RCL's to ensure timely submission/approval of PLR's in required timelines (12-18 months prior to launch) and ensure data quality of Launch Requests by resolving inconsistencies with Stakeholders: VCM Organization, GHH and GRA
  • Collect, analyze, and summarize data to support decision-making and project evaluation.
  • Support the implementation of processes related to new product introduction, following established guidelines and protocols.
  • Documentation and Reporting
Requirements
  • Bachelor's degree in supply chain, pharmaceutical sciences, business administration, or a related field.
  • 1 to 3 years of experience in the biopharmaceutical industry, with exposure to new product introduction, project management, or related roles.
  • Basic understanding of pharmaceutical product development processes, regulatory requirements, and commercialization strategies.
  • Proficiency in data analysis tools and techniques.
  • Proficiency in Microsoft Office Suite and other relevant software.
  • Proficient in the use of business software (including MS Excel, MS PowerPoint, MS Project).
  • Working knowledge of SAP and Rapid Response (prior experience with Merck MRP systems, practices/principles beneficial).
  • Basic understanding of Operations, Planning, Regulatory strategy, and Business/Financial acumen beneficial.

Thank you for considering this opportunity. I look forward to connecting with you.



NES Fircroft verfügt über mehr als 50 Jahre Erfahrung im Bereich des globalen Workforce-Management und der Rekrutierung von technischen Experten.

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