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QC Analyst - Microbiology (French Speaking)

QC Analyst - Microbiology (French Speaking)

LocationGlattpark-Opfikon,, Switzerland
Business SectorBiotechnology
Contact email
Job ref22835
Publishedabout 2 months ago
QC Analyst – Microbiology (French Speaking)

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.
  • 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.

Critical Requirements
  • 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.

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

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

Sound interesting?
Send your CV to Khanyi Mabena at k.mabena@panda-int.com or contact her on +41 445 514407.