The Sr. Regulatory Affairs Specialist will have a broad spectrum of responsibilities spanning from participation in label review, product development teams and preparation of global regulatory submissions. Key duties to include (but not limited to): Prepare and maintain Technical Files in support of global submissions. Prepare and submit submissions to obtain global approval (PMA, CE…Details
We pride ourselves on our ability to create an entrepreneurial work environment that fosters collaboration, creativity and an overall great place to work. We are consistently looking for experienced individuals who can help us expand and grow our business – if you are interested in a career at Suneva Medical submit a cover letter and resume to email@example.com. Resumes submitted by recruitment firms will not be accepted.