Kellen Giroux

With over 16 years of experience in the medical device industry, Kellen has immersed himself in various facets of Quality systems. His journey began by supporting FDA and international audits, providing a solid foundation for his subsequent roles in continuous improvement, complaint handling, and managing CAPA processes. Kellen has successfully overseen document control, internal audit, incoming inspection, and data analysis programs. Possessing certifications as a quality engineer and quality auditor, he actively contributed to new product development teams and spearheaded transitional projects aligning with both 13485:2016 and EU MDR standards. For the past 2 years, Kellen has been at the forefront of driving and leading the business development aspect of Network Partners’ Medical Device Quality vertical.