Specialist EMEA Product Life Cycle Management (m/f/d)

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Beschreibung



Specialist EMEA Product Life Cycle Management (m/f/d)

Reference: -en
Start: asap
Duration: 9 MM+

Main tasks:
  • Leading cross functional teams, managing complex information flow
  • Coordinating and integrating the functional/ tactical project management activities for New Products Launches, Network Changes, Regulatory
    driven changes with Artwork impact
  • Insert Growth and Deletions in close collaboration with Value Chain Management, Global Launch Team, Product Source management, ES-PLM and partner with E2E Planners,
    EMEA Hub functions, Portfolio Management teams across regions (NA, AP, LA) and stakeholders across divisions
  • Coordinate activities to mitigate risks related to the different milestones across the lifecycle stages including, but not limited to: PLR Approval, Code Creation, Initial RCT update, Forecast Positioning, Artwork Readiness, First Packaging/ Pack-by Readiness, in line with the Regulatory Implementation Definition, last packaging to guarantee successful launch, post approval change or deletion by ensuring system readiness 
  • Responsible for and providing end to end visibility for all projects within assigned product portfolio to all stakeholders throughout all divisions 
  • Coordinate activities to mitigate risks related to Artwork Readiness. Liaise with Regulatory Affairs, Artwork Centers and Quality for timely execution
  • Liaise within the PLM Team to identify cross functional links & risks driven by PSO initiatives & B2B Deals and drive process improvement initiatives with the global process stewards
  • Design, execute, track and report PLM KPls within Region, (Market & Regional views) mitigating risks to minimize impact to business; participate and provide input to the IBP process (Demand Reviews, Site Supply Reviews)
  • Understand & translate the chemical, formulation and 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


Main qualifications
  • Bachelor's Degree Required - preferably Supply Chain or related discipline
  • Commercial Apprenticeship or several years relevant work experience (Product Lifecycle Management/ Supply Chain management/ Supply & Demand Planning/ Manufacturing & Packaging/ Project Management/ Regulatory)
  • Experience in customer facing environments, interfacing w/ functions involved in the regulatory process
  • Experience in problem solving and task management; prior experience in project management is an advantage
  • Pharmaceutical experience is an advantage.
  • Proficient in the use of business software (including MS Excel, MS PowerPoint, MS Project)
  • Working knowledge of SAP
  • Fluent in English
  • Ability to evaluate data and information from multiple sources, organize information in a logical way and work towards solving problems independently


Main advantages:
  • Reputable international company 
  • Pleasant work environment 



About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.

My contact at Hays:

My contact person:
Yves Fabien Deschamps

Referencenumber:


Make contact:
Email:
Start
ab sofort
Dauer
9 MM+
(Verlängerung möglich)
Von
Hays AG
Eingestellt
27.05.2021
Ansprechpartner:
Hays AG
Projekt-ID:
2122784
Vertragsart
Freiberuflich
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