Quotient Limited
Eysins, Vaud, Switzerland
vor 4 Tg.
Job Description

The main responsibilities will include:

  • Perform routine Quality Control testing of incoming material, intermediate and final product
  • Analyse and record data in test records and other relevant documentation to provide a permanent and precise record of all work carried out to ensure compliance with specifications
  • Handle compliance records such as OOS investigations, CC, NC, CAPA as required
  • Write, review and update procedures to ensure compliance
  • Maintain the stability schedule. Test and review Quotient products currently undergoing stability assessment


  • Minimum 5 years’ experience working in QC laboratory (pharmaceutical, medical device or medical laboratory) and GMP experience
  • Experience in immunohematology and quality management system
  • Experience in blood group serology desirable
  • Analytical and data review skills, 
  • Excellent time management and prioritization skills, flexible
  • Good spoken and written English and French

Additional Information

Temporary replacement 6-10 months

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