Associate, Manufacturing (Night)

Associate, Manufacturing

BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions. Guided by our purpose to develop medicines that make a profound impact on people's lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions. Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world-class manufacturing capabilities. At the heart of BioMarin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world.

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.

Associate in Manufacturing at BioMarin in Novato, detailing responsibilities in a 100% cGMP manufacturing facility involving biopharmaceutical processes such as cell culture and protein purification, with required skills including process knowledge, equipment separation and experience with automated systems.

Responsibilities:

• Work in 100% cGMP manufacturing facility
• Ability to work as a team, learn and operate in biopharmaceutical manufacturing processes including cell culture, cell production and protein harvest, depth filtration, tangential flow filtration, column chromatography, protein purification and formulation of bulk drug substance; and perform all aspects with a broad understanding of scientific, compliance, and technical components

Required Skills:

• PROCESS KNOWLEDGE: Understanding or concept of pH, cell culture, bioreactors Understanding of process theory and equipment operation Understanding working as a team Support initiatives for process optimization Identify and elevate processing issues and support solutions
• Demonstrated experience with automation systems (LIMS, MES, PI, etc.)

Experience: 2 years of industry experience. Education: 4 years of college or 2 years of biotechnology program.

Shift Details: Night [Wed-Sun with every other Sat, hrs 1800-0700] (12 hr shifts)

Onsite, remote, or flexible: On Site

Travel Required: NO

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.