Lead design change activities on commercial Drug Eluting Stents/ Balloon products ensuring product safety, compliance, material continuity and cost reduction.
Works cross-functionally with project management, quality, manufacturing, regulatory, clinical and marketing to ensure project success.
Must be able to effectively work within a multidisciplinary team and the international organisation.
Works independently to plan and schedule own activities necessary to meet timelines.
Performs troubleshooting on products/process problems as related to design, material or process.
Summarizes, analyzes and draws conclusions from test results.
Prepares standard reports/documentation to communicate results to technical community.
Demonstrate a primary commitment to patient safety and product quality.
Understands and complies with all the regulations governing the quality systems.
Motivated, self-starter who works within a team environment.
Able to provide technical guidance within a large team and be an effective communicator within a multidisciplinary and international organisation.
Supports team members by setting an example, coaching and providing feedback and guidance
Qualifications
Engineering/Science Degree (Level 8), preferably Mechanical, Materials or Biomedical Engineering.
At least 8+ years in a Design /Manufacturing environment.
R&D/Technical experience preferably in the Medical Device sector.