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Technology Development and Integration Associate - Netherlands  

PharmaCell (company)


Posted on : 12 July 2017

Project Description

The position:
  • For the furthermore expanding of our Technology Development (TD) department we have an open position for a TD&I Associate.
  •  In this position you are responsible assisting the TD&I Expert during technology transfer and implementation of new assays in our facilities.
  •  In this position you are also responsible for ensuring the execution of assay, process and validation development activities.

Tasks and responsibilities:
  • Assist in the non-compendial assays transfer during technology transfer. 
  • Gain understanding of new assays in details and transfer this knowledge to our facility. 
  • Drafting and revising assay related documents as part of the method transfer and validation. 
  • Execute experimental campaigns (cell culture and assays) for the assigned projects, ensuring that activities are performed according to applicable protocols and safety standards. 
  • Support investigating equipment, material and procedure equivalency during TT 
  • Generate and process experimental data, and report all laboratory activities in relevant lab books and log books. 
  • Generate laboratory, technical, and quality documentation relevant to or resulting from transfer or development activities 
  • Carrying out laboratory associated duties e.g. orders (internal and external), and logistic activities. 

Qualifications and skills:
  • BSc, or MSc in biology, biotechnology, medical-technology or pharmaceutical sciences with preferably working experience in a QC environment. 
  • Hands on experience with cell characterization techniques (e.g. FACS, qPCR, ELISA) and cell or tissue culture techniques (traditional and preferably automated platforms) is required. 
  • Accuracy, well organized, problem solving, result driven, attention to detail, desire to work in a high paced environment, flexible, team player 
  • Awareness of GMP, Quality regulations, documentation experience is recommended. 
  • Working experience in a GMP setting (e.g QC or IVD settings) is highly recommended 
  • Strong communication skills in English.