Data scientist Jobs in Neuenburg
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Data scientist • neuenburg
- Gesponsert
QC Associate Scientist
RandstadNeuchatel, NeuchâtelSenior Data & Analytics Engineer 80%-100%
CIGES SABoudevilliers, CHChemistry Assistant (80-100%)
AQCNeuchâtel, CH- Gesponsert
Applied Ai Research Scientist
WhatJobsNeuchâtel, SchweizSr. Specialist Scientist QC Analytical Technical Support
Bristol Myers SquibbCH,Boudry- Gesponsert
E-commerce Product Owner
Adecco Human Resources AGNeuchâtel, CH- Gesponsert
Manufacturing Engineer MBR Designer
CK GroupNeuchâtel, Neuchâtel, SwitzerlandApplied AI Research Scientist
Hilo By AktiiaNeuchâtel, NE, CHQC Associate Scientist
ExperisNeuchâtelDessinateur Industriel - Data Produit
HIFI Group SA2053 Cernier, CHQC Associate Scientist
Randstad (Schweiz) AGNeuchâtel, CHData Architect - Data Product Owner
Banque Cantonale NeuchâteloiseColombier NE, CHCustomer Service & Logistics Planning Specialist 100% H / F
InterimanNeuchâtelApplied Ai Research Scientist
Consult & Pepper AGNeuchâtel, CHQC Associate Scientist / ta-330
SimplyVision GmbHNeuchatel, CHPlaces d'apprentissage Gestionnaire du commerce de détail CFC / AFP Canton de Neuchâtel
SAGMarin, CHFacharzt / Fachärztin Ophthalmologie mit Schwerpunkt Ophthalmochirurige für eine topmodernen Klinik gesucht!
Medimeo AGNeuenburgQC Associate Scientist
RandstadNeuchatel, NeuchâtelJobdescription
For our client, an international company based in Neuchâtel, we are looking for a QC Associate Scientist
General Information :
Workplace : Neuchâtel
Contract : Temporary via Randstad (6 months)
Start date : ASAP
Workload : 100%
Tasks and responsibilities :
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 :
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
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)
Your profile :
- University or engineering degree in microbiology
- Experience in GMP laboratory activities
- Experience in problem solving and deviation (event) / lab investigation management
- Strong knowledge of method validation / verification
- Expertise in critical material qualification
- Proficiency in statistical tools
- Fluency in French and English (C1 level in written and spoken)