Role Summary We are seeking a skilled Quality Specialist to manage quality records for events associated with the Secondary Packaging and Device categories. The successful candidate will serve as the primary point of contact and external supply quality record owner for our sites in Ireland and the Netherlands. This role requires strong process, operational, and scientific expertise, as well as basic compliance knowledge and analytical skills. Required Skills and Qualifications * Doctorate degree or higher**: Master's degree & 3 years of directly related experience OR Bachelor's degree & 5 years of directly related experience OR Associate's degree & 10 years of directly related experience OR High school diploma / GED & 12 years of directly related experience * Demonstrated ability to coordinate cross-functional project teams**: Experience leading multiple priorities in a fast-paced environment with minimal direction is required. * Excellent communication skills*:** Technical writing, presentation skills, collaboration productively with technical management staff, The ideal candidate should have at least 3+ years of relevant work experience (manufacturing, process development or quality assurance) in Biotech or pharmaceutical industries. h2 color":{"rgb":[0, 3]}">