At BioMarin, we are committed to creating innovative medicines that improve human health. As a Process Validation Associate, you will play a critical role in ensuring the quality and integrity of our manufacturing processes. This is an exciting opportunity for a talented individual with experience in cGMP regulated environments to join our team and contribute to the development of life-changing therapies. * Perform process validation activities related to drug substance and drug product manufacturing * Coordinate and manage process validation projects across multiple departments * Develop and implement SOPs/Guidelines documents with systematic procedural improvements Required Skills and Qualifications: