Quality Control Analyst
vor 1 Woche
We favor a close and relaxed environment. The work is carried out within a team where tasks change very quickly. You are therefore expected to be motivated by a fast-paced environment while being able to deliver high-level results.
General Information:
Start date: ASAPDuration: 9 monthsExtension: possible, to be discussedWorkplace: NeuchâtelWorkload: 100%
Tasks and responsibilities:
Carry out biochemical analysis and supervision activities according to the procedures in force in the laboratory while respecting GMP/GDP rules and/or projects related to the activities of the Quality Control departmentRespect all procedures in forceRespect and apply EHS rulesComplete the various forms, logbooks and documents while respecting Good Manufacturing and Documentation Practices and ALCOA +Notify the Supervisor in the event of non-compliant and/or invalid results the same day orally and/or in writing and initiate the event in the quality system within the allotted time frame.Manage laboratory investigationsApply planning requests and report any concerns proactively.Execute reagent/consumable qualification and validation protocols (method, system, equipment)Ensure that the calibration and maintenance of the equipment is in order during the analysisRespect the management of Kanban in real timeReport deviations on the procedure to the method/equipment manager and the Supervisor/delegate/ExpertBe able to identify and resolve certain non-complex problems relating to your area of ??expertise (Troubleshooting)Create solutions or approve solutions in the laboratoryManage and tidy up the laboratory in general, respecting 5S standardization standardsSupport continuous improvement initiatives
Your profile:
You bring strong laboratory experience, including biochemical methods such as ELISA, enzyme activity, Western Blot, etc. Through your work as a laboratory technician, you have developed a good theoretical and practical understanding of biochemical methods and technology.
Minimum level of studies: CFC laboratory/biology or another relevant scientific field.3 years minimum experience in QC laboratory in cGMP environmentExperience in Electrophoresis analysis, Elisa or determination of the desired enzymatic activityFluent French and technical EnglishYou find satisfaction and motivation in routine tasksYou work in a structured manner and with an eye for quality
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