ATVIO Careers

QC assay qualification specialist

Position No. 30

Job description
  • Laboratory focused position
  • Design, develop and implement biological QC assays for various projects according to cGMP
  • Perform data analysis and interpretation and be able to draw conclusions regarding progress and results of work, utilizing the data for appropriate decision making.
  • Writing reports and formal working documents.
  • Work on multiple projects with multiple teams
  • Perform Tech transfer from R&D to manufacturing
Job requirements
  • Master's  in engineering or PhD degree in Biology, Biochemistry and Biotechnology; or relevant experience in a similar position in the sector of biotech/pharma/cell therapy
  • Experience with Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP) 
  • Experienced with assay development including qualification and validation process.
  • Hands-on experience with cell-based bioassays, FACS and Elisa.
  • Adaptability to changing work assignments and priorities
  • Excellent teamwork
  • Excellent interpersonal and communication skills
  • Able to prioritize different activities
  • Able to identify opportunities for continuous improvements and enable implementation
  • Ability to work across a matrix team
  • Well organized, methodologic, quick learner, team player, motivated and responsible
  • Assertive and working well under pressure
  • Fluent English: oral and written, experience with scientific writing
  • This position may include occasionally traveling abroad
CV can be submitted at: info@at-vio.com