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Job Details
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Clinical Supply Chain Manager (m/f), Biotech Munich or Jena



Business Type: Biotechnology Company
Job Type: Quality Assurance - Control, Clinical Study- Trials
Job Level: Experienced (non manager)
Position: Full Time
Salary: EUR65000 - EUR85000 per annum
Location: Germany
Reference: CL10221
Closing Date: 02/05/19
Job Details:

Global (Clinical) Supply Manager (m/f)

Leading Biotech, Munich or Jena

The Company:

Our Client is a publicly listed biotechnology company headquartered in Germany with offices in Munich and in the university city of Jena. Their core focus is the research and development of treatments for inflammatory disease on a global scale. They adopt a science driven approach, and this has lead to them successfully taking several programs through pre-clinical stages through to Phase II with a healthy pipeline.

The Role:

Our Client is seeking a Global Clinical Supply Manager (m/f) who will lead the planning, monitoring, and management of the supply and demand of relevant study products as well as other study supplies. The postholder will be engaging with both internal stakeholders as well as external suppliers whilst ensuring adherence to multi-national regulations, internal SOPs, and GXP requirements. The position can be based in either Munich or Jena.

Primary Tasks:

  • Accountable for the investigational medicinal product (IMP) supply strategy, planning and organization for allocated development programs and clinical studies and ensuring key project milestones are met.
  • Represent Drug Supply and Clinical Services on internal and external Project and Study Teams.
  • Lead development and establishment of an agreed packaging specification, supply & distribution strategy with involved functions and partners.
  • Planning and coordination of activities between internal and external functions to ensure adherence to quality, timelines and on time completion of outsourced tasks/ activities.
  • For studies using IRT (or other GMP complaint IT based systems provided by 3rd party vendors employed for IMP management/ control) contributes to development and implementation of specification(s).
  • For studies using IRT (or other GMP complaint IT based systems provided by 3rd party vendors employed for IMP management/ control) contributes to development and implementation of specification(s).
  • Ensures compliance with SOPs, full GMP compliance of activities and documentation for clinical supply activities through study start through to study completion, including returns, destruction and full global traceability of Investigational Medicinal Products supplied.

Requirements:

  • Ideally you have a degree in pharmacy, Pharmaceutical Sciences, or other life sciences subject
  • You bring 2-5 years'' experience in the pharma / biotechnology industry including clinical supply project management, clinical trial supply, trial supply chain or R&D Quality Assurance.
  • Demonstrable experience in managing clinical supply chains or other clinical trial supply related activities.
  • Working knowledge of clinical supply systems and specialised tools including IXRS and experience in leading or at least in supporting project teams in the clinical supply within a CMC environment.
  • Ideally you will have had exposure to cold chain techniques for pharmaceutical products.
  • Experience in working with external suppliers, building positive relationships with them, and working in both an internal and externa matrix team environment.

For more information please get in touch with Colin Lynam via +49 (0) 89 3803 5860 or via email clynam@i-pharmconsulting.com.

If this position is not interesting for you but are interested in a new challenge, please also feel free to get in touch for a confidential discussion about potential opportunitie



Posted: 04/04/2019 | NPJ Ref: 233183
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