PM Clinical Supply Chain

Location Breda
Discipline: Biotechnology, Pharmaceutical
Job type: Temporary/Freelance
Contact name: Ralph Looijen

Contact email: r.looijen@panda-int.com
Job ref: 12068
Published: 7 days ago

One of our leading Biopharmaceutical clients in Breda has a job opening for a Project Manager Clinical Supply Chain. We are looking for someone who ideally has experience with clinical supply chain management and project management.

 

RESPONSIBILITIES

 

  • Leading the global design and set up of end-to-end customized clinical supply chains in support of the assigned clinical programs/studies.
  • Partnering with several cross-functional stakeholders.
  • Ensuring supply for global clinical trial to support first subject enrolled.
  • Provide robust inventory management tools for the clinical demand and inventory planning team.
  • Employing project management techniques to design and set up supply chains for clinical studies:
    • Create and maintain project plan to ensure timely clinical study start
    • Create and maintain study forecast for finished drug product.
    • Design optimal packaging configuration for finished drug product
    • Ensure storage and shipping capabilities plus sufficient capacity for finished drug product
    • Design cost efficient (re)supply model to distribute finished drug product via applying risk analysis and mitigation strategy.
    • Ensure efficient and smooth hand-over to clinical demand and inventory planning team
    • Facilitate the phase in phase out strategy for new medicinal product introduction

 

PROFILE

Required

  • At least University BSc degree
  • 4 years of logistics, business administration or life science experience

Preferred

  • Knowledge of clinical supply chain management
  • 5 year’s relevant working experience, preferably in the biotechnology or pharmaceutical industry, with an in-depth knowledge of supply chain management and clinical research management principles.
  • At minimum 5-year experience in project leadership and project management techniques in an international and regulated environment
  • General understanding of regulatory guidelines impacting clinical supplies (i.e. GxP, ICH guidelines, Clinical Trial Directive)
  • Fluency in English, both verbal and written communication
  • Experience in using ERP systems, preferably SAP
  • Project Management certification (PMP, IPMA)

 

START DATE

03-05-2021

 

PROJECT DURATION

12 months (extension optional)

 

INTERESTED?

If you are interested in the above description, apply with your CV

PS: Did you also know that we offer an attractive referral scheme? Check this LINK

For more information please contact Ralph Looijen on +31 (0)20 20 44 502