Descripción
For our client, an international company based in Neuchâtel, we are looking for a Quality Control Analyst.
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: ASAP
- Duration: 9 months
- Extension: possible, to be discussed
- Workplace: Neuchâtel
- Workload: 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 department
- Respect all procedures in force
- Respect and apply EHS rules
- Complete 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 investigations
- Apply 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 analysis
- Respect the management of Kanban in real time
- Report deviations on the procedure to the method/equipment manager and the Supervisor/delegate/Expert
- Be able to identify and resolve certain non-complex problems relating to your area of ??expertise (Troubleshooting)
- Create solutions or approve solutions in the laboratory
- Manage and tidy up the laboratory in general, respecting 5S standardization standards
- Support 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 environment
- Experience in Electrophoresis analysis, Elisa or determination of the desired enzymatic activity
- Fluent French and technical English
- You find satisfaction and motivation in routine tasks
- You work in a structured manner and with an eye for quality