For my client – a globally renowned biotech inNeuchâtel, Switzerland – I am looking for an experience QC Associate Scientist to join an innovative and dynamic team!
Key Responsibilities
The job holder is accountable for life cycle management activities of analytical assays performed in the QC.
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.
Execute and documents experiments
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
Requirements
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).
Practicalities
Location: Neuchâtel, Switzerland
Start Date: ASAP
Contract duration: 6-month contract – with the high chance of extension
Sound interesting? Send your CV to Khanyi Mabena at k.mabena@panda-int.com or contact her on +41 445 514 407.