QC Associate Scientist
For my client – a globally renowned biotech in Neuchâtel, 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: 1-year 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.