QC associate Level 1

4 maanden geleden


Geleen, Nederland Lonza Voltijd

Manufacturing areas, incoming materials and utility supplies and products are all released and approved for use based on QC test results as generated by the QC Associate. 

Responsible for planning and execution of daily quality assays and control activities while ensuring compliance with all existing GMP and safety standardsin the area of responsibility. 

Activities of QC Associate Level can differ per dedicated departmental responsibility whether the scope is Cell therapy, Environmental Monitoring or Raw Materials.

Environmental Monitoring:

Perform quality activities as part of Environmental monitoring

Sampling of C and/or D grade cleanroom

Perform read-out and documentation of EM results

Maintain database for EM data

Request shipments to send out positive EM samples for identification

Initiation of Quality Events as NC’s, CRF’s and EM investigations

Receive results from identification and closure or investigations

For EM, the associate is mainly responsible to assure the facility is under control for its dedicated use. Sampling, gathering data, investigating and reporting are main responsibilities.

Reference: R61517
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