Clinical Quality Assurance Jobs
Meet - , CA, United States
and develop periodic compliance/metric reports. Requirements: Bachelor's or advanced degree in Biology, Chemistry, or a related field. Minimum of 12 years of GCP/GVP Quality Assurance experience. Strong
from: linkedin.com - 12 days ago
Pliant Therapeutics - South San Francisco, CA, United States
(preferred). Quality assurance professional certification is a plus. A minimum of 5 years of experience in Clinical Quality Assurance or Clinical Operations. Broad knowledge of risk-based quality systems
from: linkedin.com - 8 days ago
Meet - , CA, United States
Job Title: Senior Director of Clinical Quality Assurance Office Location: South San Francisco (Hybrid - Tues, Wed, Thurs) Meet the Client : Meet is partnering with an Auto-Immune biotech to find them
from: linkedin.com - 11 days ago
Bayside Solutions - , CA, United States
Quality Assurance Director, Clinical W2 Contract Salary Range: $187,200 - $208,000 per year Location: Berkeley, CA - Hybrid Role Job Summary: You will be responsible for leading the development
from: linkedin.com - 8 days ago
Bayside Solutions - Berkeley, CA, United States
Quality Assurance Director, Clinical W2 Contract Salary Range: $187,200 - $208,000 per year Location: Berkeley, CA - Hybrid Role Job Summary: You will be responsible for leading the development
from: linkedin.com - 8 days ago
Meet - , CA, United States
We are partnering with an Auto-Immune biotech to find them a Senior Director of Clinical Quality Assurance. This role demands proficiency in Good Clinical Practices (GCP) and Good Pharmacovigilance
from: linkedin.com - 16 days ago
Access Medical Laboratories - Jupiter, FL, United States
The Quality Assurance Manager is responsible for overseeing and enhancing the overall quality management within the clinical laboratory. This role ensures that all laboratory processes comply
from: linkedin.com - 16 days ago
GQR - , CA, United States
Clinical Quality Assurance contract- Director level Location: San Francisco, CA Hybrid role, 2 days a week onsite Status: Contract 20-30 hours per week Direct experience working with small molecules
from: linkedin.com - 23 days ago
VRS Recruitment (US) - Nashua, NH, United States
assurance, QC, quality control, GMP, GLP, GxP, CLIA, clinical laboratory improvement amendments, good laboratory practice, quality management system, good manufacturing practice, FDA, FDA regulation, internal
from: linkedin.com - Yesterday
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