)
)
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