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QC Analyst (M/F/D)
Tasks:
Perform biochemical analysis and supervision activities according to laboratory procedures, adhering to GMP/BPD regulations and/or projects related to the Quality Control department’s activities.
Comply with all applicable procedures.
Adhere to and apply EHS rules.
Accurately complete various forms, logbooks, and documents in accordance with Good Manufacturing and Documentation Practices (GMP/GLP) and ALCOA+ principles.
Immediately inform the Supervisor of non-conforming and/or invalid results verbally and/or in writing on the same day and initiate the event in the quality system within the specified timelines.
Manage laboratory investigations.
Follow planning requests and proactively report any issues.
Execute reagent/consumable qualification and validation protocols (method, system, equipment).
Ensure calibration and maintenance of equipment are up to date during analysis.
Manage Kanban processes in real-time.
Report procedural deviations to the Method/Equipment Manager and Supervisor/Delegate/Expert.
Identify and resolve some less complex issues related to your area of expertise (troubleshooting).
Prepare solutions or approve laboratory solutions.
Maintain and organize the laboratory in general, adhering to 5S standardization norms.
Support continuous improvement initiatives.
Qualification:
Minimum education level: CFC laboratory technician in biology or another relevant scientific field.
At least 3 years of experience in a Quality Control laboratory in a cGMP environment.
Experience in electrophoresis analysis, HPLC, ELISA, or enzymatic activity determination is preferred.
Fluent French and technical English.
Swiss or EU nationality, or a valid Swiss work permit.
Requirements:
Start: 01.01.2025
Duration: 11 months
Capacity: 5 days per week
Location: Neuchatel, Switzerland
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