{"id":1387177,"url":"https://alion.io/job/iqvia-qa-auditor","title":"QA Auditor","company":{"id":4918,"name":"IQVIA","domain":"iqvia.com","url":"https://alion.io/company/iqvia","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":83,"open_postings":491,"ghost_share":0.014,"stale_share":0.811,"repost_share":0.053,"time_to_fill_p50_days":16,"computed_at":"2026-10-01T05:45:00Z"}},"role":"QA","role_family":"QA","seniority":"junior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Beijing, China"],"countries":["CN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":1,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"closed","first_seen_at":"2026-09-28T10:40:11Z","employer_posted_date":"2026-09-28","last_verified_at":"2026-10-01T05:05:08Z","board_verified":false,"closed_at":"2026-10-01T05:05:08Z","days_open":2,"trust":{"level":"not_scored","repost_count":null,"flags":[],"days_open":2},"description":"Job Overview\nAssist lead auditors/audit liaisons in conducting, hosting and reporting quality assurance audits by performing specific audit tasks under the direct supervision of more senior QA staff.\nEssential Functions\nAssist in conducting quality assurance audits within budget and established timelines by scheduling, conducting, reporting, and closing audits as directed by the lead auditor. Activities may include contacting auditees to agree on audit dates, making appropriate entries in QA database , performing data reviews, file audits as directed\nEntering and categorizing audit/Inspection findings in eQMS,\nSoliciting follow-up information and closing audits/inspection findings in the QA database.\nReview and approval of Corrective and Preventative Action (CAPA) and Effectiveness Check (EC) plans\nSupport Investigators derogatory status management in the database, prepare and release guidance document with compliance information and maintain the QA repository with compliance information for investigators with derogatory status\nAssist in hosting customer audits, mock regulatory inspections, and regulatory facility inspections by acting as a scribe. Reviewing documents, identifying and calling operational staff to answer related questions. Performing required administrative duties including tracking of documents reviewed, scheduling audit team members for interviews and coping and stamping documents for release to the auditors/inspectors.\nObtain a fundamental knowledge of current relevant GLP regulations, guidelines, and related auditing techniques.\nProvide QA consultancy where possible\nMaintains the electronic quality management system (eQMS) and provides support in relation to the audit lifecycle.\nQualifications\nBachelor's Degree Pref\n1 year Quality Assurance experience in pharmaceutical, technical, or related area, including GXP and/or Quality Assurance experience. Equivalent combination of education, training and experience. Req\nKnowledge of word-processing, spreadsheet, and database applications..\nConsiderable knowledge of GXP regulations and quality assurance auditing techniques..\nStrong interpersonal skills.. Excellent problem solving skills..\nEffective organization, communication, and team orientation skills..\nAbility to initiate assigned tasks and to work independently..\nAbility to manage multiple projects..\nAbility to establish and maintain effective working relationships with coworkers, managers and clients.\nIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com\nIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.","description_format":"text","description_chars":3342,"description_truncated":false,"requirements":{"experience_years_min":1,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":false},"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Clinical Trial Services (CRO)","Health Data & Interoperability"],"lifecycle":[{"event":"open","at":"2026-09-28T10:40:11Z"},{"event":"close","at":"2026-10-01T05:05:08Z"}],"liveness":null,"pay":null,"html_url":"https://alion.io/job/iqvia-qa-auditor","json_url":"https://alion.io/job/iqvia-qa-auditor.json","meta":{"generated_at":"2026-10-01T11:45:39Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","usage":{"tier":"crawler","counted_by":"address","units_charged":1,"used_today":3526,"day_limit":5000,"remaining_today":1474,"minute_limit":60,"resets_at":"2026-10-02T00:00:00Z"}}}