Quality Auditor - Established Pharmaceuticals Division

pWithin Abbott's Established Pharmaceuticals Division (EPD), we provide high-quality, trusted medicines that improve access to healthcare around the world. /ppbThe Opportunity /bbrLees de informatie in deze vacature zorgvuldig door om precies te begrijpen wat er van potentiële kandidaten wordt verwacht.brAbbott is seeking a bQuality Auditor /b to support supplier and third-party manufacturer oversight for EPD. Based in bWeesp /b, this role plays a critical part in ensuring compliance, quality, and regulatory adherence across Abbott's external partner network. /ppYou will manage on-site audits and quality assessments for a broad range of suppliers and third-party manufacturers, working closely with internal stakeholders and external partners to drive continuous improvement and ensure patient safety. /pWhat You'll DoulliPlan, prepare, conduct, report, and close on-site audits for suppliers and third-party manufacturers supporting EPD. /liliManage Quality Questionnaires for suppliers and third-party manufacturers and resolve any identified issues. /liliAssess, track, and follow up on Corrective and Preventive Actions (CAPAs) to ensure timely and effective closure. /liliEnsure all audit activities and outcomes are accurately documented in the Audit Tracking system. /liliProvide timely audit updates to management and stakeholders, escalating critical findings in line with policies and procedures. /liliMonitor regulatory developments, standards, and industry trends and integrate them into audit activities. /liliSupport EPD manufacturing sites in resolving supplier-related quality and compliance issues. /liliAct as the primary quality contact for external partners on auditing matters and promote a proactive quality mindset. /li /ulWhat You'll BringulliBachelor's degree in a relevant scientific or technical discipline (e.g. Chemistry, Pharmacy, Biology, Microbiology, Engineering) or equivalent industry experience. /liliAt least 8 years’ experience in the pharmaceutical, healthcare, or regulatory environment, including a minimum of 3 years of auditing experience (GMP, GDP, ISO). /liliStrong knowledge of ICH guidelines, GMP standards, WHO guidance, and applicable regional and local regulations. /liliProven experience auditing suppliers and/or third-party manufacturers across pharmaceutical, medical device, or nutrition product types. /liliStrong analytical skills with the ability to identify compliance risks and drive effective corrective actions. /liliExcellent communication skills with advanced written and verbal Business English. /liliHigh level of integrity, independence, adaptability, and cultural awareness, with willingness and ability to travel internationally. /li /ulWorking at AbbottpAt Abbott, you can do work that matters, grow and learn, care for yourself and your family, be your true self, and live a full life. You will have access to career development opportunities within an international company recognized as a great place to work in multiple countries. Abbott has been named one of the most admired companies in the world by Fortune and is recognized for its commitment to diversity, inclusion, and innovation. xgiwjmb /ppWe are an equal opportunity employer and value diversity in our workforce. We welcome applications from all qualified individuals regardless of gender, age, ethnicity, religion, disability, sexual orientation, or any other characteristic protected by law. /pbr