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Consultant CMC Development Small Molecules - Netherlands  

3DPharmXchange (company)


Posted on : 30 June 2017

Project Description

  • Our company  is a Dutch Life Sciences consultancy and operational support firm.
  • We are dedicated to the development of pharmaceuticals and diagnostics. 
  • Our team of experts covers the key areas of pre-clinical, clinical, CMC, regulatory affairs and project management.
  •  In addition, we provide out-licensing and interim management support. 
  • Our clients are leading big pharma companies as well as innovative biotech start-ups.

  •  For the various projects that we are running for our clients, we are looking for a consultant Chemistry Manufacturing and Control (CMC) development Small Molecules.
  •  As a consultant, you will work on the development of pharmaceutical compounds, are able to look beyond borders and have an ambition to grow in a young, expanding and dynamic organization. 
  • The development, manufacturing, and analytics of drug substances and drug product will generally be performed by external parties. 
  • Therefore, selection and control of CMOs will be an important part of your task.
  •  In addition, you are responsible for the entire CMC development and for writing development reports, protocols, and documents for regulatory purposes.

  • MSc or PhD in the area of (Analytical) Chemistry, Pharmaceutical Sciences, or Process T0echnology
  • At least 5 years of experience in a comparable position and/or work environment is preferred
  • Essential communication skills: fluency in English, oral, written and presentation skills
  • Extensive experience in writing development reports, protocols, and documents for regulatory purposes
  • Essential personality skills: pro-active, team player, entrepreneurial, can-do mentality and ability to put yourself in the position of our clients