Remote
•
Yesterday
The ideal candidate will have a solid background in medical device design controls and product development, with direct experience in regulatory compliance and documentation. You'll play a key role in refining existing documentation and ensuring continued regulatory alignment to support new and existing products. Candidates must have experience with software as a medical device (SaMD). Requirements 5+ years of experience Strong Experience with Software as a Medical Device (SaMD) Strong experien
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Contract
Depends on Experience






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