(CW) Research Associate 2

Who We Are

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.

About Worldwide Research and Development

From research and discovery to post-market clinical development, our R&D engine involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with rare diseases.

• Perform and document scientific experiments in collaboration with cross-functional stakeholders as part of the BCoE or Site strategy, and/or in support of BioMarin’s commercial & clinical product portfolio.

• Executes defined procedures independently to support BCoE studies and investigation activities with lab scale upstream processes in the multi-product lab.
• Demonstrates quick learning of core scientific techniques, principles, and protocols; owns small project portions with reliable execution and summarizes findings.
• Understands the principles of aseptic operation and has experience working in biosafety cabinets.
• Possesses experience in daily operations with microbial cell culture (E. coli), including:
• Cell thawing
• Cell banking
• Seed train expansion
• Has experience in fermentation processes, including:
• Fermenter inoculation
• Daily monitoring
• Sampling
• In-process analysis utilizing standard bioprocess analytical equipment
• Has a basic understanding of mammalian cell expansion and its differences compared to microbial operations.
• Experience in processing of inclusion bodies is desirable.
• Produces accurate, reproducible data entries and maintains laboratory quality through adherence to safety standards and SOPs; able to troubleshoot common problems with guidance.
• Expands technical toolkit by adapting and troubleshooting process steps or assays; applies appropriate methods and interprets basic data trends.
• Updates and refines SOP/BPD documentation.
• Assists in drafting concise technical summaries.
• Understanding of fed-batch and perfusion bioprocesses is desirable.
• Experience in depth filtration and ultrafiltration is desirable.
• Understanding of downstream purification processes is desirable.

• Executes and completes projects independently.
• Generates and reviews data; performs data analysis.
• Maintains up-to-date documentation of laboratory work, including storage and archiving in accordance with GLP.
• Supports updates of lab instructions, BPDs, SOPs, and templates.
• Supports maintenance and calibration of lab equipment with accompanying documentation.
• Contributes to the evaluation of new equipment.
• Acts as a team player with excellent communication skills.
• Plays an active role in maintaining and enhancing workplace and laboratory safety.
• Complies with applicable GxP regulations, SOPs, HSE, and other laboratory guidelines.
• May be required to work periodically outside normal business hours, including weekends.

• Adherence to project plans and deliverables
• Adherence to applicable GxP and EHS requirements
• Technical reports executed on time and to quality standards
• Efficient technical exchange with Project Leads

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.