Drug Regulatory Affairs Jobs in Santa Clara, CA

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Director, CMC Regulatory Affairs  

Bayside Solutions - Santa Clara, CA, United States (+1 location)

related field is preferred. 15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC

from: linkedin.com - 14 days ago

Regulatory Affairs Senior Manager - Vascular (on-site)  

Abbott Laboratories - Santa Clara, California

, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents. This Regulatory Affairs Senior Manager position is an onsite opportunity working out of our Santa

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from: resume-library.com - 3 days ago

Senior Regulatory Affairs Specialist - Vascular (on-site)  

Abbott Laboratories - Santa Clara, California

, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents. This Senior Regulatory Affairs Specialist position is an on-site opportunity working out

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from: resume-library.com - 3 days ago

Senior Medical Director, Clinical Development  

Sonoma Biotherapeutics - South San Francisco, CA, United States

of potential partnering and lifecycle options. The Sr Medical Director shares medical expertise with his/her counterparts in other functional areas (e.g. regulatory affairs, research, drug safety, clinical

from: linkedin.com - 14 days ago

Senior Director Regulatory Affairs  

Meet - Redwood City, CA, United States

Senior Director, Regulatory Affairs (Generalist) Hybrid Role - 3 Days in Menlo Park, CA Meet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs

from: linkedin.com - 17 days ago

Manager, Regulatory Affairs - Job ID: 1322  

Ascendis Pharma - Palo Alto, California

viewpoints and perspectives to all aspects of the business, from drug development to marketing. The Manager, Regulatory Affairs will be responsible for supporting and developing global regulatory strategies

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from: resume-library.com (+1 source) - 3 days ago

Quality Assurance Specialist - GMP  

Integrated Resources, Inc ( IRI ) - Newark, CA, United States

, and will be interacting with cross-functional groups such as Quality Control, Manufacturing and Regulatory Affairs. ESSENTIAL DUTIES: • Perform a wide variety of quality assurance activities to ensure compliance

from: linkedin.com - 22 days ago

Biotech quality assurance specialist  

Harvey Nash - Newark, CA, United States

, such as batch record and quality control data review, line clearances, AQL inspection, and will be interacting with cross-functional groups such as Quality Control, Manufacturing and Regulatory Affairs. ESSENTIAL

from: linkedin.com - 22 days ago

Senior Manager, Clinical Trials Supply Management (US or Canada)  

Jazz Pharmaceuticals - Palo Alto, California

to clinical site(s) Contribute to CTSM budget and forecasting; track invoices to contracts Provide to Regulatory Affairs any applicable information or sections of IND/IMPD/CTA/etc. submissions Knowledge

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from: resume-library.com - 19 days ago

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Quality Assurance Specialist  

SPECTRAFORCE - Newark, CA, United States

and Regulatory Affairs. Essential Duties: • Perform a wide variety of quality assurance activities to ensure compliance with company’s procedures, applicable US and international regulatory requirements

from: linkedin.com - 22 days ago


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