QA Specialist - Biotechnology
Suisse romande
Qualitätswesen; Wissenschaften
Vollzeit (100%)

  • Coordinate and perform batch record disposition for manufactured products
  • Review and approve compliance of records: 
  • Perform independent quality evaluation of investigational reports including root cause analysis cause/preventive action identification, CAPA effectiveness check and trending
  • Review and approve deviations, CAPA’s, change controls, Quality Control OOS
  • Participate in project teams to support GMP compliance for the projects.
  • Support shop floor : Quality Oversight in manufacturing and Quality Control Labs, solve issues real time with operations personnel, etc.
  • Review and/or approve SOPs
  • Lead and assist continuous improvement projects, interacts with Team Leader, peers, internal customers, external clients and other cross functional peers to gain alignment on sound quality decisions
  • Provide cGMP and associated training to QA and other departments to improve right the first time (RTFT), high quality performance
Your Profile:
  • Bachelor or Master degree or engineer
  • Minimum 5 years of experience in Quality Assurance Operations in pharmaceutical or Biotechnology company
  • Experience with Quality Systems to include, Batch Record design/review and supporting investigations
  • Good organization skills and attention to detail, with strong verbal and written communication skills
  • Fluent English is required, French is highly desirable
Your Kelly contact :

Sophie Darthenay,
Consultant Professional Staffing Life Science
Engineer in Biology
Kelly Scientific Geneva