Please refer to JobSuchmaschine in your application
QC Raw Material Lead Investigator - 18 months
As a Lead Investigator based in Nyon, you will be part of the QC Raw Material team with the responsibility for leading the Trackwise activities and support QC Raw Material Supervisor in planification of analysis.
Your responsibilities include in detail:
•Manage all trackwise activities (Deviations, Change-Controls, CAPAs, Compliance records)
•Investigate in case of OOS results or deviations, in collaboration with the QA for QC Compliance Officer
•Perform full root cause analysis with the analysts and define the investigation plan with the QA for QC Compliance Officer
•Write deviations in Trackwise in French and English
•Ensure that investigations are processed on time
•Support planification of analysis in collaboration with the Supply Chain
•Update Raw Materials KPIs
As a successful Lead Investigator, you have a good experience of working in a QC laboratory, with proven ability to treat several topics in parallel.
Furthermore you display the following qualifications and competencies:
•Minimum 5 years’ experience in a Pharmaceutical QC laboratory
•Proven Analytical Technical understanding (Titration, Spectrophotometry, physico-chemical measurements and Chromatography)
•Proven experience in Raw Materials analysis
•Good experience in analytical investigations and technical writing
•Good knowledge of European Pharmacopeia and cGMP
•Ability to demonstrate leadership
•Safety, Quality, Result and Customer oriented
•Good English level (B2)
You may apply for this position online by selecting the Apply now button.
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