Description

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.

Manufacturing Associate BioProcess Specialist

Closing date 17th January 2025

• All core responsibilities of current Manufacturing Biotechnician role.
• Actively support the Bioprocess Specialist as a Point of Contact with the Manufacturing Biotechnician role.
• Leading and supporting investigation and resolution of process investigations as required.
• Rapid response troubleshooting of Process specific equipment and escalations.
• Training of Biotechnicians on operational OJTs including awareness training, Instructor led training and additional training as required.
• In depth knowledge of operational control systems in respective operational areas.
• Have an SME understanding of the applicable process control documentation.
• Gather and provide required information for the escalation pathway to support clear communications through the tier levels and support Process team decisions.
• Support inspections/audit where required.
• Assisting with writing, review and revision of manufacturing documentation as necessary. (e.g. deviations, standard operating procedures and test scripts etc.)
• Other duties as assigned.

Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned. 

Equal Opportunity Employer/Veterans/Disabled

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.