BioMarin has experienced substantial growth organically since its inception, primarily over the last decade. While this steady growth in both cost structure and staff was essential to BioMarin's emergence as a leading, fully integrated global biopharma with approximately $2 billion in revenues from over 75 countries, a robust R&D pipeline, operating profits, and world cla

The Head of Global Cyber Security is responsible for BioMarin's overall cybersecurity strategy, personnel, processes, and technologies. Reporting to the Senior Vice President and Chief Information Officer, Information Technology, this senior level role will be a key member in the IT Leadership Team, providing cybersecurity oversight and guidance for BioMarin. The Head of

Provide technical oversight for product (s) manufacturing/testing executed at external and internal partners. Act as Technical Development technical representative on process teams. Act as an SME on biologic Drug Product, including technology transfer, process validation, trouble shooting and investigation on specific product(s). Participate in cross functional teams, as

Shift Details Swing shift, 4 10hr shifts (Wednesday Saturday) 11am 10pm onsite in Novato, CA The Quality Control Microbiology (QCM) Supervisor is responsible for supervising a GMP laboratories supporting microbial test and release of drug substance intermediates from biopharmaceutical manufacturing from cell culture up through final formulation and the environmental monit

Who We Are 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 ensur

Who We Are 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 ensur

Department Leadership and Management Collaborate with QC Functional Head and People Department to identify needs and participate in recruiting, hiring, and promoting staff Lead and develop a cohesive, balanced, and high functioning team focused on producing high quality deliverables and outcomes Optimize the organizational design and allocation of team resources across th

The Senior Technical Manager is part of the Novato Quality Compliance group reporting to the Head of Compliance. The role is responsible and accountable for establishing and maintaining Novato's self inspection program for all GMP areas including clinical manufacturing and testing areas including network services that are managed out of the Novato site. This position will

Provide on the floor QA oversight and support to manufacturing operations Review executed batch records and associated document to ensure compliance with approved procedures and cGMP expectations Respond to quality related incidents or non conformances on the floor and secure necessary documentation for real time investigations Represent QA in support of deviations includ

Provide on the floor QA oversight and support to manufacturing operations Review executed batch records and associated document to ensure compliance with approved procedures and cGMP expectations Respond to quality related incidents or non conformances on the floor and secure necessary documentation for real time investigations Represent QA in support of deviations includ

ThisSenior Accountantrole is part of theU.S.Controllershipteam, with a focus on the accounting for theTechnical Operations (TOPS) function.This role will be reporting to the Director,U.S.Controllership, and be part of a great team who values flexibility, excellence, integrity, and work life balance. We are a global company with teams across the US, EUCAN, ICON, and other

This S enior Accountant role is part of the U . S . Controllership team , with a focus on the accounting for the WWRD (World wide Research and Development) function . This role will be reporting to the Director , U . S . Controllership , and be part of a great team who values flexibi lity, excellence, integrity, and work life balance. We are a global company with teams ac

This Manager Level role will support the execution of the WWRD GxP Audit Program with heightened focus in pharmacovigilance audit related responsibilities. Primary Responsibilities Participate in audit planning including internal or external audit risk assessment, audit scheduling, development of audit scope/agenda, and managing pre audit meetings Host and manage internal

The Head of Novato Quality Compliance is part of the Novato Quality Leadership team (NQLT), reporting to the Site Head of Quality and is accountable for all GMP compliance activities for the Novato Site and network services that are managed out of the Novato site. The Associate Director of compliance is a pivotal role in setting the GMP compliance tone for the Novato Site

The Senior Technical Manager is part of the Novato Quality Compliance group reporting to the Head of Compliance. The role is responsible and accountable for establishing and maintaining Novato's Manufacturing Quality Management System Review as well as establishing and executing site Annual Product Review (APR) programs. This position will be responsible for establishing