Benjamin Dumke Email & Phone Number

Saint Paul, Mn, Us

Five years as a Clinical Laboratory Scientist executing numerous diagnostic methods as "customer" proved invaluable throughout the last 7 years as an assay developer responsible for personally fostering immunoassay innovations from feasibility to market release. As an individual contributor, I have been fortunate to escort individual products from conceptual phase to international in-vitro application. Success in R&D efforts resulted in larger system based project roles, providing greater insight to regulatory, in addition to technical obstacles, which typically restrain new product development.My greatest asset is my ability to efficiently design and execute experimentation by thorough and accurate facilitation of functional purpose statements-paired with high level of competency with instrumentation.

Proficient in following, testing, and revising Standard Operating Procedures (SOPs).Experienced in a highly regulated work environment.Follows Current Good Manufacturing Practices (CGMP), safety practices (AABB, OSHA),confidential policies and regulatory guidelines (FDA, EU).Performs quality control procedures, proficiency testing, clinical trial validation,qualification testing, and investigational protocols with extreme attention to detail.Responsible for laboratory equipment calibration, maintenance, and validation protocols.