Summary
Leads and/or manages mid-high complexity programs in R&D.
Lead cross-functional teams in a matrix organization.
Plans projects, directs and coordinates the efforts of engineers and non-technical project team members.
Generates and maintains development schedules.
Interacts with management in R&D, Clinical/Regulatory Affairs, Customer Care, Marketing, Operations, Quality Assurance, and Supply Chain to ensure successful product development and introductions.
...
Seeking succesful track record ensuring regulatory and ISO 13485 comliance and getting regulatory approval for medical devices to manage content, assembly, pre-final review, and filing of medical device applications.
Required Experience:
*** IDEs
*** PMAs
*** 510(k)s
Generous benefits package includes 401(k) plan which matches $1.00 for each dollar contributed, and qualified retirement plan company contributes % of eligible pay to the accounts of all eligible employees; medical, dental, ...
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