Extensive Medical Device experience, in particular within non-clinical test and validation disciplines, having worked both in planning, executing and reviewing (QA) protocols, statistical data analysis and reports.

Several post-warning letter remediation projects.
Recreation of lost component specifications.

Used for risk-and statistics-based rationalesand justifications for complex problems as well as effectiveness checks for CAPA’s.

He believes that there will be a solution to every problem and will always strive to offer a feasible way onwards (or alternatives with pros and cons in cases where several viable solutions exist).

He is assertive by nature and will listen and look to data to offer the best way going forward, be it in a validation project, in writing up a lean QMS system or assessing the state of compliance and how to remedy any gaps.

He likes to keep up to date with new standards and regulations in the MedTech industry.
In his spare time he enjoys reading and spending time in his toolshop.