Company : Pharmiweb Location : Ghent Flanders From : Talent BE
You will have the opportunity to work with Biologics (ATMP) products.
Key duties:
Completion of QC testing related to the manufacturing of cell therapy products for clinical trials/commercial operations in a controlled cGMP cleanroom environment Ensure compliance with all applicable procedures, standards and GMP regulations Work with the Process Development team, Quality and Operations functions to transfer process/analytical testing to a cGMP facility to manufacture products Conduct analytical testing of raw material/utility either in process or final product samples as submitted to the QC laboratories Use of electronic systems (LIMS) Create, review and approve relevant QC documents, SOPs and WI's Key requirements for the QC Analyst role:
Bachelors Degree in Science, Engineering or equivalent technical subject Minimum of 3 years work experience in a cGMP environment Experience of QC testing/EMS is required Fluent technical English language skills Able to work shift patterns of 4 days on, 4 days off covering either early or late shifts on rotation.
The shift partnern is much more preferable to most on offer in the market Again if you are not based in Belgium, and are interested in relocating from elsewhere within the EU/ UK please do get in touch.
Nicole Buckland Executive Consultant:
Quality Management and Technical Operations 02031890467/ 07923646762 NBuckland@i-pharmconsulting.com Pharmiweb GhentFlanders
