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OPERATIONS - ENGINEERING/PRODUCTION
QC Investigation Specialist
Permanent contract
Role Overview
The QC Investigation Specialist is an exempt level position with responsibilities for leading deviations and corrective actions in support of the QC testing laboratories related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment.
Major Responsibilities:
In this function you will be responsible to manage the QC related deviations and execute qualitative investigations in close collaboration with the analysts and the involved stakeholders according to the required procedures. Ensuring thorough root cause analysis is performed using the correct tools and proper CAPAs are defined in order to reduce non-conformances and deviations in the future. Different tasks are (but are not excluded to)
Life sciences
Education:A minimum of a Bachelor’s Degree in Science, Engineering or equivalent technical discipline is required and relevant years of experience within the pharmaceutical industry.
Experience:A minimum of 4 years relevant work experience is required. It is preferable that the candidate have experience working in an aseptic manufacturing facility, preferably in quality control, quality assurance, manufacturing compliance, clinical quality, or cell therapy.
Capabilities, Knowledge, and skills:
Europe, Belgium, Flanders, East Flanders
3 to 5 years