GCP Auditor

Plans,schedules, conducts and follows up on GxPAudits of Perrigo Sites, Material Suppliers, Contract Operations or Contract Service Providers to assure Perrigo and its business partners comply with applicable cGxP.  Applies appropriate GxP standard based onlocation / where marketed and function.  Depending on expertise may lead GCP (clinical), GDP (distribution), GLP (laboratory), GMP (manufacturing) or GPvP (Pharmacovigilance)audits to US FDA, MHRA, EMA, TGA or other local regulatory authority standards.    Leads or participates in assigned projects to establish or improve corporateaudit and/or quality compliance governanceprocesses to assure robustprocessesmet stakeholder expectations. Must possess thorough understanding of, and ability to interpret, GxP regulatory requirements relative to one or more country/region that Perrigo operates or markets product Subject matter expertise in one or more area of GxP (e.g. GMP, GCP, GLP, GPvP) relative to medical and/or nutritional product development, manufacturing and/or supply chain Strong analytical and interpersonal skills, commanding oral and written communication ability Self-directed and able to work effectively across multiple global cultures in a matrix environment Ability to influence management, peers and other colleagues without direct reporting lines Bachelor's degree in a scientific discipline or closely aligned field Ten plus years of experience in GxP regulated industry, at least five of which is in GxP audit / compliance Quality Auditor designation/certification preferred Requires significant domestic and international travel (approximately 60%)
Salary Range: NA
Minimum Qualification
11 - 15 years

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