#2406194384W
ire system lifecycle, from initial concept and requirements gathering to development, verification, and submission.
Prepare, present and lead design reviews to attain agreement on project with peers and cross-functional review team.
Lead team for excellence in the development and update to design documentation including test protocols, reports, and engineering summary to support both quality and regulatory submissions.
Foster a collaborative and innovative work environment within the team, promoting effective communication, problem-solving, and knowledge sharing.
Resolve producibility issues with internal and external manufacturing partners. Work with internal and external manufacturing partners to ensure producible designs and processes (DFM).
Perform evaluations, design and prototyping using CAD (Solidworks), FEA, 3-D printing to accelerate development and engineering of plastics, ceramic, composite and metallic parts, electromechanical systems.
Qualifications
Education:
BS in Mechanical Engineering or directly related scientific field, MS Preferred.
Experience and Skills:
Required:
12 years experience.
Proven track record of successful project delivery on time.
Excellent leadership and communication skills, with the ability to motivate, guide, and build trust with a team. Ability to communicate ideas and information clearly, effectively, and frequently (oral and written) with stakeholders, project team, local and international.
Strong analytical and problem-solving skills, with the ability to identify and implement solutions to complex technical challenges.
Experience working in a collaborative and cross-functional environment.
Preferred:
Product development experience in Class 3 Medical Device engineering
Experience in Mechanical Circulatory System manufacturing, design and development
MSc/MEng Preferred
Applied understanding of DFM concepts and manufacturing best practices
Working knowledge of SAP and Minitab desired.
Other:
English required
May require up to 10% travel - US & EU
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