CD cGMP Manufacturing facility and cGMP Warehouse is in a state of quality and regulatory compliance at all times.
Impart training to employees working in cGMP regulated areas of CDWork with all support functions in closing off deviations, CAPA,
Around 12-15 years in Process QA.
Should have worked in international pharmaceutical companies.
Should have faced US FDA and MHRA audits
Knowledgeable in GAMP .
Single Point Of Contact (SPOC) to liaise with QA on quality system documentation