Mark Kielek

Vice President, Quality Assurance and Regulatory Affairs

Mr. Kielek joined Svelte Medical Systems in 2008 and has over 30 years of diversified experience in the manufacturing of medical devices and pharmaceutical products.

Prior to Svelte he worked at Johnson & Johnson for 13 years building and leading quality organizations at McNeil Consumer Healthcare, Johnson & Johnson Medical and Ethicon Endo-Surgery.  Mr. Kielek also worked at Schering-Plough Corporation directing the establishment of effective quality systems resulting in the successful remediation of the company’s consent decree.  He also held quality leadership positions at The West Company, Playtex, Inc., and National Pharmaceutical.

Mr. Kielek holds a BS in Zoology from the University of Maryland.