Who We Are
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.
About Technical Operations
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.

• System Owner for some site Utility Systems
• Site SME for clean utilities system with overall responsibility for the compliant operation of critical clean utilities.
• Support the start-up of all facility utilities (clean and black) during project and planned shutdown works
• Ensure all HVAC systems are running in line with critical area classification standards and parameters
• Utilize Six Sigma tools such as root cause analysis methods to establish root causes to any issues that may arise and implement robust corrective measures.
• Responsible for ensuring that all utilities remain operational, available for use and GxP compliant at all times.
• Setup and review of contracts with BioMarin Legal and QA Representatives.
• Input into site utility master planning efforts to ensure utility design and capacity can meet site and business needs.
• Ensure that maintenance & calibration is carried out in accordance to cGMP regulations, safety considerations and site quality standards.
• Generate, report and analyse key utility metrics.
• Use of permit to work system or other safety systems to control engineering activities.
• Participation in HAZOP, FMEA and design reviews.
• Support the site Energy Management and Sustainability works
• Ensure that all engineering drawings and documentation are maintained in compliance with relevant cGMPs and GEPs.
• Raising, investigating and closing site quality records such as change requests, deviations, events and actions.
• Identify all critical spare parts required for equipment.
• Development, control and forecasting of site energy budget.
• Planning and execution of site utility shutdowns
• Other duties as assigned