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Quality Control Scientist

m/w/d, Neuenburg

The job holder is accountable for life cycle management activities of analytical assays performed in the QC Laboratories.

Start date: ASAP

Duration: 6 months/possible extension

Validation and Qualification Activities

Author transfer protocols and reports for assays
Author qualification plans and reports for critical reagents
Oversee validation and qualification activities executed by analysts, provide
Execute and documents experiments

Investigation Leads

Investigate and trouble shoot problems which occur to determine solutions or
Recommendations for improvements or change
Conduct/participate in risk assessments, root cause analysis and investigations
Own Laboratory Investigations and CAPA

Quality Control Support Activities

Support the application of industry specific compliance standards/regulations to
Assays life cycle management activities
Participate to daily activities upon request (provide technical and statisticalsupport)

Experience Required

University or engineering degree in analytical chemistry, biotechnology, biochemistry
2 years of experience in GMP
Experience in Validation management is mandatory
Experience in authoring protocols is mandatory
Very good knowledge of method transfer
Very good knowledge of critical reagent qualification
Experience in problem solving and deviation management
Good Knowledge of statistical tools
Fluent in French and English (C1 written and spoken)