Independent/Freelance GxP Auditor (GCP, GMP, GLP, GVP, CSV)

Seeking: Independent GxP Consultants - (i.e., GCP, GCLP, GLP, GMP, GVP, CSV)Advarra Consulting has the responsibility to perform independent audits, covering Good Clinical Practice, Good Laboratory Practice, Good Manufacturing Practice, and Good Pharmacovigilance Practice. Advarra is seeking Independent GXP auditors, with experience and expertise in clinical research, quality assurance and other diverse areas to effectively provide service and project deliverables.Auditor Engagements (may include any of the following) Investigator Site Audits CRO Audits GxP Vendor AuditsGxP TrainingInspection Readiness Assessment and TrainingInspection Readiness Visits to Investigator Sites for Client-specific contracted projectsMock Regulatory Inspections at Client facilitiesQuality Tool Development (Storyboards)Inspection Support at Client facilitiesGxP SOP Gap AnalysesGxP SOP DevelopmentRequirementsEducationBachelor’s Degree or four (4) years equivalent experience ExperienceMinimum of ten (10) years clinical research and/or R & D experience in pharmaceutical, biotech, medical device and other life science industries. Minimum of seven (7) years working knowledge and experience in Quality AssuranceKnowledge/Skills/AbilitiesStrong GxP knowledge; (i.e., GCP, GcLP, GLP, GMP, GVP, CSV)Proficient in the use of Microsoft OfficeFamiliarity with industry specific software and systems used in research and developmentCollaboration with internal and external partners to include understanding client requirements and deliverablesAbility to communicate clearly and professionally in English (verbal, written, and presentation)