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MicroPort Orthopedics, Inc.
- Arlington, TN / Burlington, MA / Los Angeles, CA / 38 more...
As Regulatory Affairs Specialist II, you will be responsible for preparing US and International regulatory submissions. You will be responsible for development, maintenance, and review of submissions, documentation, labeling, and procedures. Required Skills, Knowledge and Abilities Basic knowledge of FDA and applicable international regulations, preferred Ability to work independently and/or with
Posted 1 day ago
MicroPort Orthopedics, Inc.
- Arlington, TN / Burlington, MA / Los Angeles, CA / 37 more...
As Sr. Regulatory Affairs Specialist, you will prepare global regulatory submissions and communicate regulatory strategies to product development teams. You will also be responsible for development, maintenance, and review of submissions, documentation, labeling, and procedures. Skills Requirements Proven leadership skills Ability to work with minimal to no guidance from management to perform job
Posted 1 day ago
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