Quality Auditor - Established Pharmaceuticals Division

ppWithin Abbott’s bEstablished Pharmaceuticals Division /b (EPD), we provide high‑quality, trusted medicines that improve access to healthcare around the world. /p h3The Opportunity /h3 pAbbott is seeking a bQuality Auditor /b to support supplier and third‑party manufacturer oversight for EPD. Based in Weesp, this role plays a critical part in ensuring compliance, quality, and regulatory adherence across Abbott’s external partner network. /p pYou 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. /p h3What You’ll Do /h3 ul liPlan, prepare, conduct, report, and close on‑site audits for suppliers and third‑party manufacturers supporting EPD. /li liManage Quality Questionnaires for suppliers and third‑party manufacturers and resolve any identified issues. /li liAssess, track, and follow up on Corrective and Preventive Actions (CAPAs) to ensure timely and effective closure. /li liEnsure all audit activities and outcomes are accurately documented in the Audit Tracking system. /li liProvide timely audit updates to management and stakeholders, escalating critical findings in line with policies and procedures. /li liMonitor regulatory developments, standards, and industry trends and integrate them into audit activities. /li liSupport EPD manufacturing sites in resolving supplier‑related quality and compliance issues. /li liAct as the primary quality contact for external partners on auditing matters and promote a proactive quality mindset. /li /ul h3What You’ll Bring /h3 ul liBachelor’s degree in a relevant scientific or technical discipline (e.g. Chemistry, Pharmacy, Biology, Microbiology, Engineering) or equivalent industry experience. /li liAt least 8 years’ experience in the pharmaceutical, healthcare, or regulatory environment, including a minimum of 3 years of auditing experience (GMP, GDP, ISO). /li liStrong knowledge of ICH guidelines, GMP standards, WHO guidance, and applicable regional and local regulations. /li liProven experience auditing suppliers and/or third‑party manufacturers across pharmaceutical, medical device, or nutrition product types. /li liStrong analytical skills with the ability to identify compliance risks and drive effective corrective actions. /li liExcellent communication skills with advanced written and verbal Business English. /li liFluency in Dutch is required, with the ability to communicate professionally with local stakeholders in the Netherlands. /li liHigh level of integrity, independence, adaptability, and cultural awareness, with willingness and ability to travel internationally. /li /ul h3Working at Abbott /h3 pAt 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. /p pWe 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. /p h3Recruitment Process /h3 pWe are conducting recruitment on an ongoing basis and will close the process as soon as the right candidate is found. /p pIf you meet the qualifications and are interested in this opportunity, we encourage you to apply as soon as possible. /p /p #J-18808-Ljbffr