Sr. Associate QA

pJoin a Leading Biopharmaceutical Organisation /p pWe are seeking a detail-oriented bSenior Associate Quality Assurance (QA) /b to support quality operations within a highly regulated pharmaceutical manufacturing environment in Breda, Netherlands. This is an excellent opportunity for a quality professional with GMP experience who enjoys working with cross-functional teams, ensuring compliance, and maintaining high-quality standards for medicinal products. /p pThis position offers the opportunity to contribute to critical QA processes, including SAP Master Data review, artwork approval, SOP management, and continuous quality improvement initiatives. /p pbContract Duration: /b 7 November 2026 – 6 May 2027
- strong possibility of an extension /p pbLocation: /b Breda, Netherlands /p pbLanguage Requirement: /b Fluent in Dutch and English /p h3bKey Responsibilities /b /h3 pQuality Assurance Compliance /p ul liPerform QA review and approval of SAP Master Data activities, including critical value verification and Bills of Materials. /li liReview and approve artwork for medicinal products. /li liEnsure compliance with GMP and applicable regulatory requirements. /li liMonitor and maintain QA systems and quality processes. /li /ul pDocumentation Quality Systems /p ul liAuthor and maintain operational SOPs and Work Instructions. /li liConduct QA review and approval of SOPs and related documentation. /li liSupport data integrity initiatives and investigate quality-related issues. /li liAssist with investigations, root cause analysis, and corrective actions as required. /li /ul pPerformance Continuous Improvement /p ul liPrepare weekly and monthly quality metrics and reports. /li liMaintain departmental performance boards and KPI tracking. /li liParticipate in QA projects and process improvement initiatives. /li liBuild effective working relationships with Global Artwork Centre, Master Data teams, Regulatory Affairs, Supply Chain teams, SMEs, and QA leadership. /li /ul h3bWhat We're Looking For /b /h3 pRequired Qualifications /p ul liMBO or Bachelor's degree in Life Sciences, Pharmaceutical Sciences, Biotechnology, or a related field. /li liApproximately 3 years of Quality Assurance or pharmaceutical manufacturing experience. /li liKnowledge of GMP, GDP and/or GCP regulations. /li liExperience working within a regulated pharmaceutical or medical device environment. /li liStrong attention to detail and high level of accuracy. /li liExcellent communication skills in English. /li liAbility to manage priorities and perform effectively under pressure. /li /ul h3bPreferred Qualifications /b /h3 ul liDutch language proficiency. /li liExperience reviewing SAP Master Data. /li liArtwork approval experience within the pharmaceutical industry. /li liExperience with SOP writing and document management processes. /li /ul h3bWhy Apply? /b /h3 ul liGain experience within a globally recognised biopharmaceutical organisation. /li liWork in a highly collaborative and quality-focused environment. /li liContribute directly to patient safety and product quality. /li liDevelop expertise in pharmaceutical compliance, artwork management, and master data governance. /li /ul #J-18808-Ljbffr