QA Validation Specialist - GMP & Validation Lead

BioMarin Pharmaceutical Inc. is seeking a QA Validation Associate in Ireland for a 12-month contract. The role includes providing quality oversight for validation activities in a cGMP regulated environment. Candidates should have a Bachelor's degree in a technical discipline and 3+ years of experience with validation processes and techniques. Responsibilities encompass developing validation plans and supporting project lifecycle documentation. A strong understanding of regulatory requirements is essential, along with excellent organizational and communication skills.