$80K - $100K*
BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. Come join our team and make a meaningful impact on patients' lives.
This position reports to the Assoc. Director Global Process Validation and is responsible for any of biological, gene therapy, or small-molecule process validation activities in a cGMP environment which can include drug substance and drug product processes. This position will coordinate and manage process validation projects related to the implementation of new manufacturing proce
Valid through: 2020-5-20
$200K - $250K
12 days ago