Cinta Burgos has been involved in the Biotech and Medical Device industry since 1993; working in various positions in research engineering, validation engineering, and Quality Assurance in large companies as well as small start-ups. Prior to entering the industry she was a microbiology laboratory researcher. Ms. Burgos is an independent QA consultant for several biotech and medical device companies, supporting GLP and GCP laboratories and studies; responsible for developing and maintaining Quality Systems from Design Control/Product Development to cGMP manufacturing; conducting ISO, GMP, and GCP audits, managing complaint, risk, and corrective action systems, training, due diligence, a...
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