Associate Director, Precision Medicine Quality & Design
Stevenage, England, United Kingdom
Hybrid / WFH Options
Hybrid / WFH Options
Workday
GCLP, CLIA, CAP, ISO15189 laboratory requirements Experience in CLSI, NYDOH and other industry standards for assay validation; Understanding of IVD regulations including QSR regulations, GMP manufacturing, ISO13485, and FDA and EU medical device regulations. Preferred Qualifications & Skills: Please note the following skills are not necessary, just preferred, if you do more »
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