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a Technical/Scientific Writer Ghent Belgium,  

Pharmavize (company)

Posted on : 27 May 2017

Project Description

  • Our company  is a Contract Research & Development Laboratory that serves pharmaceutical companies worldwide. 
  • It assists tier-one pharmaceutical companies as well as starting companies.
  • The company's expertise spans human as well as veterinary medicinal applications.
  • Services are tailored to deliver value in the fields of R&D, Preclinical and Clinical Material Manufacturing, Quality Management and Regulatory Support.
  • Our team of researchers develops innovative and cost-effective analytical methods, formulations and processes. 
  • Moreover, we assist customers in developing registration dossiers and we provide them with quality management support whenever needed. 
  • The company services apply to Active Substances as well as to Drug Products.
  •   For our Regulatory Department we are looking for a TECHNICAL/SCIENTIFIC WRITER in field of PHARMACEUTICAL FORMULATION DEVELOPMENT

Job description
  • You are part of the Consultancy Team that brings tailored and timely services to our customers.
  • You will be responsible for writing scientific documents and technical reports related to pharmaceutical development.
  • You ensure full compliance with regulatory requirements. You re reporting to the Division Manager Services.

Main responsibilities
  •   Interpret data related to pharmaceutical formulation development scientifically and statistically  
  •   Write technical customer reports as well as CMC regulatory documentation based on raw data generated by pharmaceutical companies  
  •   Solve problems and issues by offering practical solutions that are compliant with regulatory requirements 
  •   Remain up-to-date on all new laws and regulations concerning pharmaceuticals and medical devices 

  •   You have a Master s degree in a Pharmaceutical Sciences; a PhD degree is a big plus  
  •   Prior knowledge of state-of-art chemical, pharmaceutical, process and analytical technologies  
  •   Proven experience with scientific and or technical writing for chemical and/or biopharmaceutical drugs, knowledge of medical devices legislation is advantageous  
  •   You have excellent writing and presentation skills with attention to detail and accuracy 
  •   You re able to handle multiple projects and to adapt to changing priorities 
  •   You re a team player 
  •   You re fluent in English 

  •   You will be working in a highly innovative and challenging environment where we encourage personal development and team play 
  •   We offer you a competitive salary and benefits package 


Mariakerke Ghent Belgium

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