For my client – a globally renowned biotech in Neuchâtel, Switzerland – I am looking for an experience QC Analyst to join an innovative and dynamic team!
Description The work consists of carrying out analysis and supervision activities according to the procedures in force in the laboratory, respecting GMP rules and/or projects related to the activities of the Quality Control department.
Perform analyses or analysis approvals in the QC laboratory according to applicable procedures and standards, for example, cGMPs and pharmacopoeias, based on planning priorities.
Respect all rules described in the SOPs applied in the laboratory.
Execute laboratory activities with the current SOP open.
Complete various forms, logbooks, and documents respecting Good Manufacturing Practices and Documentation + result management system(s).
Notify the Supervisor/delegate/Expert in case of non-conforming and/or invalid results on the same day verbally and/or in writing and initiate the event in the quality system within the specified deadlines.
Report any deviations from the schedule to the responsible person and Supervisor/delegate proactively.
Complete Smart QC at the beginning and end of each activity.