San Antonio, Texas 510(k) wizard FDA Med Device


 The Newell Group is recruiting on behalf of an innovative, rapidly-growing biotech firm in the San Antonio, TX area for

Regulatory Affairs Manager Regulatory Affairs Specialists


Successful senior candidates will have experience leading teams through the FDA regulatory process for Medical Devices

All candidates will have experience with 510K, RFD, FDA 21, CFT 820, UDI and other regulations in the context of biomed/med device products TRF, RFD, UDI CAPA, QA,

5+ years minimum experience FDA Regulated Device/ Regulatory Experience


Degree in Biological sciences or closely related field required- Master’s Preferred.


Compensation includes base of 85-95k level In addition to a competitive base, these roles include bonus, health, vision, dental and other benefits.



Please submit your resume and if we find a match, we’ll reach out for more info


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