Responsibilities
Include but are not limited to the following: 
• Define, create and communicate a commercialization path for new medical devices or pharmaceutical product solutions from concept creation through product development.
• Create documentation to define system requirements and specifications, managing internal and external stakeholders, through development, validation, documentation and release of products.
• Leads cross-functional project execution for platform technologies, ensuring compliance with ISO 9001 and ISO 13485 standards
• Act as a customer-facing representative for platform technologies, including participation in industry trade shows and technical discussions
• Collaborate with internal stakeholders including R&D, Regulatory, and site teams to ensure successful delivery of services related to pre-clinical to Phase II within oral solid dose drug development
• Assist in North America product sustainability as a techni...