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Scientist (M/F/D)
Tasks:
Laboratory Investigations
Critical Material Qualification
Laboratory Method Transfers
In addition, the job holder also supports daily QC activities following cGMP, policies and EHS requirements.
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 training and support
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 statistical support)
Qualification
University or engineering degree in analytical chemistry, biotechnology, biochemistry
1 or 2 years of experience in GMP pharma business activities, preferably in the scope of recombinant
therapeutic product in pharmaceutical environment
Experience in GMP Laboratory activities
Good knowledge of method transfer
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)
Proficiency in all aspects of standard IT tools
Requirements:
Start: 12.01.2027
Duration: 8 months
Capacity: 5 days per week
Location: Neuchatel, Switzerland
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