QC Analyst - Microbiology (French Speaking)

• 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.
• Execute reagent/consumable qualification protocols.
• Execute validation protocols (method, system, equipment).
• Perform recalculations in the result management system.
• Reconcile controlled documents and print if applicable.
• Enter results and supervise external laboratory results.
• Inform the equipment manager if any discrepancies are identified in the equipment.
• Conduct regular GEMBAs in the laboratory.

• Minimum CFC in microbiology or equivalent experience in pharmaceutical or biotechnological industries.
• 2-5 years' experience in a cGMP laboratory or minimum 2 years as an analyst I.
• Minimum 5 years' experience in a cGMP laboratory or minimum 5 years as an analyst II.
• Good knowledge of laboratory methods.
• Very good knowledge of laboratory methods.
• Good knowledge of cGMP.
• Knowledge of Data Integrity aspect.

• Comfortable with common IT and office tools (Office suite).
• French and English (technical).
• English (minimum B2).

• Location: Neuchâtel, Switzerland
• Start Date: ASAP
• Contract duration: 6-month contract - with the high chance of extension

Panda International