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)