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Quality Analyst (M/F/D)
Tasks:
Develop solutions for the various QC Analytical analyses
Potentially carry out biochemical and HPLC analysis and supervision activities in accordance with laboratory procedures, GMP/BPD rules and/or projects related to QC department activities
Comply with all procedures in force
Respect and apply EHS rules.
Complete various forms, logbooks and documents in compliance with Good Manufacturing and Documentation Practices and ALCOA +.
Notify the Supervisor of any non-conforming and/or invalid results on the same day, orally and/or in writing, and initiate the event in the quality system within the set deadlines.
Manage laboratory investigations.
Apply planning requests and report any concerns proactively.
Carry out reagent/consumable qualification and validation protocols (method, system, equipment).
Ensure that equipment calibration and maintenance is in order during analysis.
Respect real-time Kanban management
Report procedural deviations to the Method/Equipment Manager and Supervisor/Delegate/Expert.
Be able to identify and solve certain fewer complex problems relating to his/her area of expertise (troubleshooting).
Produce solutions or approve solutions in the laboratory.
Manage and tidy the laboratory in general, respect 5S standardization standards.
Support continuous improvement initiatives
Qualification:
You work in a structured, quality-oriented way.
You find satisfaction and motivation in routine tasks.
You have experience of good manufacturing practice (cGMP) - Minimum level of education: CFC laboratory/biology or other relevant scientific field.
Experience in HPLC/Elisa is a plus.
Fluent French and technical English
Requirements:
Start: asap
Duration: 6 months
Capacity: 5 days per week
Location: Neuchatel, Switzerland