At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.\nAs guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.\n*Job Function**\nQuality\n*Job Sub Function**\nQuality Assurance\n*Job Category**\nProfessional\n*All Job Posting Locations:**\nAllschwil, Basel-Country, Switzerland, Beerse, Antwerp, Belgium, High Wycombe, Buckinghamshire, United Kingdom, Issy-les-Moulineaux, France, Milano, Italy\n*Job Description***As a Specialist, QA Clinical Auditor you will:**Leads the planning, conduct and reporting of GCP QA routine audits and supports non-routine GCP audits including Clinical Investigator Site audits, Trial/Program audits, External Service Provider audits, Process/System audits, Local Operating Country audits, to assure adherence to corporate policies, internal standards/requirements and compliance with applicable regulatory requirements. Non-routine audits include Due Diligence, for cause audits, cross-functional, complex/sensitive system/service provider audits as defined by the scope.Ensures the relevant standard procedures, audit tools, and audit plans are fully understood and applied in audit activities.Analyses, interprets data and identifies patterns and trends in data sets.Ensures timely and appropriate review & delivery of CAPAs and actions arising from audits.Presents information logically and concisely, both verbally and in writing, including writing reports with clarityProvides GCP Audit strategy support, especially on QA risk-based auditing approach (Audit plans)Supports regulatory inspections in various supporting roles.Completes assigned training requirements in a timely manner to ensure inspection readiness at all times.May assist in the preparation of training material if requested.Participates in projects or serves on teams, as assigned by supervisor.Meets priorities, checkpoints, and timelines for all aspects of work and projects to achieve adequate progress.*Qualifications/Requirements**A minimum of a Bachelor’s degree is required. Advanced degree in scientific, medical or related subject area is preferred.Experience working in Clinical Quality & Compliance, Clinical Operations, and/or related R&D; area is required.Knowledge of the drug development process, applicable regulations, R&D; practices, and scientific and quality terminology.Knowledge of Good Clinical Practices (GCP) and applicable regulations/guidelines (e.g. FDA regulations, EU CTR, ICH E6 R3Understanding of fundamentals of clinical trial risk management.Broad knowledge of management of standard operating procedures, good documentation practices, and records management.Digital literacy & Analytics - Experience using standard applications/systems & data analytics tools.Ability to plan and prioritize work in an efficient manner, and to work well under time constraints.Must be able to speak and write in English.This position may require up to 30% of domestic and/or international travel.\nThis role can be located in any of the main J&J; offices in EU.\n*Required Skills***Preferred Skills:**\nBusiness Alignment, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Data Analysis, Detail-Oriented, Goal Attainment, Human-Centered Design, Internal Controls, Issue Escalation, Problem Solving, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards