Bachelors or foreign equivalent degree in Engineering, Biology, Chemistry, Life Sciences, or in a closely related scientific or engineering field of study with at least 1 year of professional experience in i cGMP regulations for medical devices andor biologics, ii escalating complaints to Quality Incident andor Corrective and Preventive Actions CAPA investigations based on complaint investigation findings; and iii managing complex programs and database software including Excel data queries with PowerBI, Salesforce, and other document control systems such as Agile and ENSUR.
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