What are the responsibilities and job description for the Senior Regulatory Affairs Specialist position at Real Staffing?
A tenured Medical Device Client of mine local to the San Diego area is looking for a full-time Senior Regulatory Specialist professional to join their growing RA / QA team! Here you will be able to author 510k and ROW submissions for a SaMD / Implant device, assist with global regulatory strategies, and act as the technical lead for the Regulatory department.
Read on to find out what you will need to succeed in this position, including skills, qualifications, and experience.
Successful candidates will have the following :
- 5 years of Medical Device Regulatory experience
- Authorship or Co-authorship of 510k submissions
- Experience working with implantable or software-based (SaMD) medical devices
- Experience working with both Pre and Post market regulatory functions and submissions
- Able to come on site
Apply now for immediate consideration!
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