Regulatory Affairs Specialist - FDA Submissions & GMP
Grifols, S.A
Grifols, S.A is seeking a Regulatory Affairs Specialist to manage regulatory documents and compliance at their Vista, CA facility. The successful applicant will handle tasks such as maintaining documentation for deviation reports and assisting with FDA submissions. This position requires an Associate's degree, advanced computer skills in Microsoft Office, and at least 5-10% travel. Benefits include a competitive salary between $80,546 and $120,819, medical coverage, PTO, and professional growth opportunities. #J-18808-Ljbffr Grifols, S.A
Vacancy posted 2 days ago
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