Description

In this role, you will serve as the technical liaison for endoluminal reprocessing solutions, conducting research, engaging with stakeholders, and ensuring compliance while advocating for customer needs throughout product development.

Requirements

• •Bachelor’s degree in science, engineering, or related field, or equivalent relevant experience
• •Demonstrated experience or strong interest in medical procedures and reprocessing, with applicable certifications
• •Minimum 4 years of industry experience with proven track record of translating customer needs into actionable design insights
• •Experience working directly with customers to articulate value of new medical technologies
• •Demonstrated success collaborating with international, cross-functional teams across multiple time zones
• •Experience navigating complex or high-tension situations, aligning stakeholders toward effective solutions
• •Excellent written and verbal communication, presentation, and interpersonal skills
• •Acts as a Medical Device Consultant in Austria and Germany after appropriate training
• •Willingness and ability to travel up to 60%, often on short notice
• •Fluency in English and German

Tasks

• •Execute exploratory reprocessing research programs
• •Develop and implement project plans for research programs
• •Collaborate with commercial, clinical, and market teams to prioritize expansion targets
• •Engage stakeholders and conduct site assessments to understand local reprocessing needs
• •Deliver tailored information sessions and ensure compliance with local regulations
• •Monitor outcomes and share learnings with leadership for continuous program improvement
• •Gather feedback from end users and external partners during early-stage product development
• •Identify customer challenges and advocate effective solutions
• •Support validation and launch strategies with hands-on field training and feedback collection
• •Review documentation to ensure clarity and compliance as a Subject Matter Expert