Quality Analyst (M/F/D)
Tasks:
* Carry out biochemical analysis and supervision activities according to current laboratory procedures, in compliance with GMP/GDP rules and/or projects related to the Quality Control department’s activities.
* Comply with all current procedures.
* Comply with and apply EHS rules.
* Complete various forms, logbooks, and documents in compliance with Good Manufacturing and Documentation Practices, as well as ALCOA+ principles.
* Inform the Supervisor immediately (the same day, verbally and/or in writing) in the event of non-compliant and/or invalid results, and initiate the event in the quality system within the required timeframes.
* Handle laboratory investigations.
* Follow planning requirements and proactively report any issues.
* Execute qualification protocols for reagents/consumables and validation (methods, systems, equipment).
* Ensure that equipment calibration and maintenance are up to date before analysis.
* Follow Kanban management in real time.
* Report deviations from procedures to the method/equipment manager and the Supervisor/delegate/Expert.
* Be able to identify and resolve some less complex problems related to your area of expertise (troubleshooting).
* Prepare solutions or approve solutions in the laboratory.
* Organize and maintain the laboratory in general, following 5S standardization norms.
* Support continuous improvement initiatives.
Qualification:
* Minimum education level: CFC laboratory technician/biology or another relevant scientific field.
* At least 3 years of experience in a QC laboratory in a cGMP environment.
* Experience in electrophoresis, HPLC, ELISA, or enzyme activity determination is desired.
* Fluent French and technical English.
* Swiss or EU nationality, or valid Swiss work permit.
Requirements:
Start: asap
Duration: 6 months
Capacity:5 days per week
Location: Neuchatel, Switzerland
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