Our Team

Natalie J. Kennel, RAC, ASQ CQE & CQMgr

Natalie founded NJK & Associates, a medical device consultancy, to bring her practical perspective to medical device quality and regulatory affairs.

With more than 25 years in industry She has hands-on experience with development, manufacturing and Regulatory Affairs/Quality Assurance (RA/QA) as well as having served in clinical roles in both major and start up medical device companies.

Since forming NJK & Associates in 2005 she has submitted more than thirty 510(k)’s and numerous Pre-Submissions, set up quality systems for client companies, and provided on-going RA/QA services. She has prepared numerous international medical device submissions for Australia, Europe, Canada, and Singapore. She set up quality systems and currently provides regulatory affairs support for a novel tissue bank.

Natalie has been published in RAPS regarding clinical trials for medical devices. She has spoken at several industry organization conferences including SDRAN, ASQ and ACRP on multiple regulatory, quality and clinical topics. She is past president of SDRAN.

For the past 12 years she has taught the medical device submission section for the U.S. RAC study group, and regularly teaches a software validation seminar for the USC regulatory affairs master’s program.

Natalie holds a BS degree in Chemical Engineering from the University of Rochester.

Roger Greenwald

Roger became a partner in NJK & Associates in 2007, after a decades long career working in industry.

His industrial experience includes work in R&D, product development, manufacturing, and quality assurance. Along the way he earned over 50 US patents, most for medical devices.

A seasoned teacher, Roger brings a hands-on leadership style to his work, helping your people in understanding what the regulations demand and how to satisfy them in a straightforward manner.

His experience in problem solving and root cause investigation has helped clients to discover and fix issues, often before they became customer problems or reportable events.

He has helped clients with all aspects of medical device and IVD projects, from product development to manufacturing, from creating to maintaining a culture of compliance. He provides valuable insights to your management team by performing internal, due diligence, and supplier audits.

Roger holds a BS in physics from Northeastern University and an MS in optics from the University of Rochester.

Visit his LinkedIn profile to learn more.