Senior GCP Auditor

Benefits

Additional Information

Company Overview ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient's immune system and treat the host rather than just the disease. Why ImmunityBio? - ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases. - Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California. - Work with a collaborative team with the ability to work across different areas of the company. - Ability to join a growing company with professional development opportunities. Position Summary The Senior GCP Auditor ensures GCP compliance with ImmunityBio entity standard operating procedures, ICH and US FDA regulations and guidelines, and clinical study protocols. This position interacts cross-functionally with functional teams in Clinical Trials which include Clinical Operations, Regulatory, Pharmacovigilance, Medical Writing and Data Management to ensure compliance to the GCP Quality Management System and all applicable regulatory requirements. This role is responsible for maintaining inspection readiness at all times. Essential Functions Maintain and update the Clinical Trial Quality Management system to be current with industry standards, guidance, and best practices. Contributes to the development and review of SOPs and other controlled documents (forms, templates, work instructions). Ensures compliance with SOPs and ICH GCP E6 (R2) standards. Manages the incident management program through monitoring of complaints, deviations and CAPAs. Schedules, plans, coordinates, and conducts vendor/supplier audits, internal audits, compliance visits, for cause audits and clinical trial site audits. Prepares required documentation to support audit activities including audit plans, audit reports, audit certificates and corrective action plans Validates accuracy of audit findings, a written audit report and follow-up activities to assure that non-compliance issues are addressed with satisfactory resolution. Reviews the final audit documents for accuracy. Review trial related documents e.g. protocols, protocol amendments, ICFs, pharmacy manuals and CSRs Apply regulations, guidance document requirements, and study protocol requirements to clinical trial studies. Participate in solving GCP compliance issues within Quality Assurance, Clinical Operations, Regulatory Affairs, Medical Affairs, and Pharmacovigilance. Support joint efforts in training on company procedures, GCP regulations, and documentation systems to assure compliance with company policies and regulatory standards. Maintain all associated QA department spreadsheets tracking of deviations, CAPAs, complaints, audit findings, and audit files as applicable. Lead development and implementation efforts for inspection readiness at all times. Assists senior staff during regulatory inspections or other audits. Represents QA department at internal and external meetings supporting clinical programs. Performs other Quality related duties, as assigned. Education & Experience Bachelor's Degree in a life sciences or engineering discipline with a minimum of 7 years of experience in a GCP-Biologics or Pharmaceutical environment; or Master's degree in a life sciences or engineering discipline with a minimum of 4 years of experience in a GCP-Biologics or Pharmaceutical environment CQA or other audit certifications are a plus Prior TMF or electronic document management systems experience is a plus Knowledge, Skills, & Abilities Ability to effectively plan and organize work activities and prioritize task completion to meet schedules and deadlines Strong problem solving and analytical skills with demonstrated ability to be detail-oriented, while managing multiple projects simultaneously. Demonstrated understanding and application of ICH GCP E6 (R2) Proficient in communication both verbal and written Multitasks across multiple functional areas Timeline focused and flexible in their work scheduling to meet the demands of a multi-product clinical phase pharmaceutical company. Working Environment / Physical Environment This position works remote Flexibility in working schedule, i.e., off-hours, second shift, weekends 25%-30% travel may be requ