Posted to MedZilla on 3/30/2017


Switzerland, Senior Quality Control (QC) Analyst SC_NP_10489-MZ


This is an exciting new opportunity for a Senior Quality Control Analyst to join a research-led, global pharmaceutical company. Our client, who focuses on the discovery and development of novel biological entities (mAbs) and Biosimilars, is based in Switzerland and is looking for a Quality Control - Senior Research Officer specialising in Biologics. This is a permanent role based in Western Switzerland. 

Job Role:

You will be responsible for executing tests for GMP and PD projects in the bio-chemical laboratory and participating in general QC activities.

Job Responsibilities:

  • Execute testing for cGMP projects, development, validation, tech transfer and stability programs.
  • Contribute towards the maintenance and continuous improvement of procedures, techniques and equipment used in the QC department.
  • Perform data analysis and trending.
  • Initiate laboratory investigations for OOS and change controls where necessary.
  • Provide support and execute method trouble shooting.
  • Provide independent organization of operational activities in the QC laboratories according to the local HSE and quality guidelines.
  • Write documentation for work performed: generic analysis, data logging, generic/method validations studies, change requests, deviations and out of specifications.

Job Requirements:

  • You must have strong experience in HPLC/UPLC techniques and relevant Biologics experience in an industrial setting under GMP, as well as, knowledge of current analytical techniques is a requirement.
  • Hands on experience in analytical method development of therapeutic biologics are a plus.

If you would like more information about this great opportunity to work with a leading biopharma, please get in touch with Nisha Patel on 0203 861 8210 or via email on [click here]">[click here]. A full job description will be available on request. 

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