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The R&D Packaging Engineer III will drive the commercialization of new products and design changes for current products through development, qualification, and launch phases. The role involves using technical expertise to develop novel medical devices, including concept development, device verification and validation, and root cause analysis.
Job Responsibility:
Lead R&D deliverables throughout the medical device design control process
Collaborate with a cross-functional team to plan, develop, modify, implement, and support IPD products
Develop technical plans, guide design inputs, conduct feasibility studies, refine product designs, verify and validate subsystems and systems
Transfer designs to Manufacturing and Operations and support global Regulatory filing strategies
Execute design verification testing to confirm design outputs meet requirements
Demonstrate knowledge of packaging product design, development, and control processes
Requirements:
5 years of work experience or 3 years plus an advanced degree in ISO 11607, ASTM Packaging Standards, and Medical Device Packaging Design
Experience with medical device design control processes and maintaining design documentation
Proficiency in SolidWorks or equivalent CAD tools
Strong critical thinking and project management skills
Ability to manage multiple projects simultaneously
Capability to work effectively in cross-functional teams
Knowledge of DFSS principles and/or Six Sigma tools (Kaizen, process improvement)
BS in Mechanical Engineering, Materials Engineering, or Biomedical Engineering
Strong communication skills, both verbal and written
Demonstrated ability to work effectively within a cross-functional team