Monitor and check that the Manufacturing Procedures are being completed in full accordance with cGMP procedures and that all the relevant checks are performed in order to verify that the documentation has been performed according to GDP guidelines.
To carry out the manufacture and production on site of pharmaceutical intermediates/products according to BMRs, ensuring Environmental, Health and Safety precautions are being adhered to whilst working within the defined production areas.
To operate the production facilities in a safe and proper way in compliance with cGMP and all other company procedures and practices.
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