QC Associate Scientist (m/w/d)
Dieses Jobangebot ist nicht länger verfügbar.
Neuenburg, Schweiz |
Temporary Employment
Zu besetzendes Projekt: QC Associate Scientist
Branche: BiotechFähigkeiten: QC,Life Cycle Management
Projektstart: asap
Projektdauer: 12 months
Einsatzort: Neuenburg, Schweiz
Duties:
The job holder is accountable for life cycle management activities of analytical assays performed in the QC
Laboratories of Neuchâtel – Switzerland with a focus on:
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
Quality Control Support Activities
Experience:
Laboratories of Neuchâtel – Switzerland with a focus on:
- Laboratory Investigations
- Critical Material Qualification
- Laboratory Method Transfers
- In addition, the job holder also supports daily QC activities following cGMP, Takeda 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)
Experience:
- University or engineering degree in analytical chemistry, biotechnology, biochemistry, microbiological
- 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
Referenznummer: 15538
Branche: Biotech
Beginn des Projekts: asap
Dauer: 12 months
Anstellungsart: Temporary Employment
Kontakt
Luca Furler