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Regulatory Affairs Specialist I
San Jose, CA within
Senior Clinical Quality Assurance Specialist
Pharmacyclics, LLC -
Conduct investigations of GCP-related issues (i.e., product complaints) and develop corrective ... Work in collaboration with clinical sites, Clinical Operations, Regulatory Affairs and othe...
Jobs2Careers - 253 Days ago
IT Quality Specialist III
I.T. Solutions, Inc. - Foster City, CA, USA
... FDA regulatory requirements. • Maintains programs and processes to ensure high quality products and compliance with current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (...
CareerBliss - 11 Days ago
Medical Director/Sr. Medical Director US Patient Safety...
AstraZeneca Pharmaceuticals LP - San Mateo, CA, USA
The role holder also collaborates with US and Global Patient Safety, Medical Affairs, Regulatory ... Provides US PS input to product global safety governance teams (i.e., SSaMTs) * Contribut...
BioSpace - 4 Days ago
Application Support Specialist
Title21 Health Solutions - Pleasanton, CA, USA
Understand the compliance challenges, regulations and processes (i.e. Error Management, Hemavigilance, CAPA, PM/Calibration, Audits, etc.) * As a Technical Specialist, configure and validate the&...
ZipRecruiter - 976 Days ago
Sr Philanthropic Specialist (SWS Sr Advisory Spclst (LO...
Wells Fargo US - Palo Alto, CA, USA
... i.e. accountants, attorneys, who are related to the client relationship as part of day to day ... Individuals in a LO position also must meet the Loan Originator requirements under ...
eFinancialCareers - 4 Days ago
Medical Director/Sr. Medical Director US Patient Safety...
AstraZeneca Pharmaceuticals LP - Redwood City, CA, USA
The role holder also collaborates with US and Global Patient Safety, Medical Affairs, Regulatory ... teams (i.e., SSaMTs) Contributes to the content of the Safety Sections of the US Prescrib...
CareerBliss - 3 Days ago
Senior Document Control Specialist
Revance Therapeutics, Inc. - Newark, CA, USA
... and regulatory guidelines. Works on assignments that are complex in nature where judgment is ... i.e. general to complex) for the Electronic Document Management System (EDMS). Provi...
CareerBliss - 4 Days ago
Medical Director, Clinical Science
Pharmacyclics, LLC -
Supports Regulatory Affairs on clinical development aspects of filings; plays a central role in ... In-depth understanding and firsthand knowledge of Phase I-III drug development. * Broad ex...
Jobs2Careers - 60 Days ago
Medical Director
Pharmacyclics, LLC -
Supports Regulatory Affairs on clinical development aspects of filings; plays a central role in ... In-depth understanding and firsthand knowledge of Phase I-III drug development. *Broad exp...
Jobs2Careers - 79 Days ago
Sr. Clinical Research Associate
Pharmacyclics, LLC -
Collaborates with internal cross functional teams (i.e., Clinical Science, Biometrics, Regulatory Affairs, etc.), to ensure effective delivery of the assigned project milestones * Organizes and ....
Jobs2Careers - 60 Days ago
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