Responsible for remotely supporting Iovance’s GCP quality system. • Support GCP quality system activities including clinical quality events, deviations, CAPAs, supplier corrective action requests, investigator site audits, service provider audits, internal audits, clinical change controls and regulatory inspections. • Identify opportunities to increase the efficiency and effectiveness of the GCP QMS. • Support training activities and back-up efforts for clinical quality assurance processes. • Maintain updated knowledge and relevant assessments of the GXP landscape, regulations, and guidelines pertaining to GCP quality assurance. • Some travel required (approximately 10%).
Iovance Biotherapeutics, Inc. is HIRING A
Clinical Quality Assurance Associate II
📍 United States 🌐 Fully Remote ⏰ Full TimePlease mention you found this job on TestDev Jobs. It helps us get more people to hire on our site. Thanks and good luck!
Please mention you found this job on TestDev Jobs. It helps us get more people to hire on our site. Thanks and good luck!