Jose Cardenas

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quality assurance regulatory affairs clinical affairs medical device pharmaceutical biotech training iso9001 iso13485 iso17025 permanent placement supplier audits quality audits business consulting & services technical consulting services talent acquisition global supplier audit compliance management risk management supplier management clinical trials fda submission iso standards gmp compliance mock audits efficacy testing process optimization design controls technical writing market entry strategy pharmaceutical services biotechnology consulting diagnostics support clia labs process validation quality management systems capa training continuous improvement talent networking industry expertise audit protocols regulatory strategy supplier quality agreements clinical protocols global compliance risk analysis data integrity quality system audits clinical site audits post-acquisition integration technical due diligence human resource consulting operational excellence regulatory compliance engineering consulting strategic partnerships supply chain audits performance metrics hospital & health care medical management consulting health care health wellness & fitness writing & editing