To join our Life Sciences team in Neuchâtel, we are looking for a Quality Control Specialist (F/M) in the pharmaceutical sector.
The job holder is accountable for life cycle management activities of analytical assays performed in the QC Laboratories with a focus on:
- Laboratory Investigations
- Critical Material Qualification
- Laboratory Method Transfers
In addition, the job holder also supports daily QC activities following cGMP, client's 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
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 statistical support)