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.

• Acts as lead for at least 1 commercial program Critical Reagent portfolios.
• Author critical reagent technical documentation, including protocols and reports for qualification, requalification, expiry extension, qualified ranges, etc.
• Perform review and data verification of technical documentation.
• Maintains critical reagent trending graphs to monitor material stability, assay performance and suitability of qualified ranges, and to support technical documentation
• Maintains critical reagent inventory and participates in forecasting of critical reagents supply demands and identifying resupply trigger points.
• Responsible for critical reagent acquisition, preparation, qualification testing coordination and release for use.
• Supports critical reagent distributions for the global testing network.
• Authors documentation, data compilation and analysis for regulatory submissions (BLA, MAA, etc.) and response letters (RTQs, etc.) for commercial products.
• Utilizes LIMS to document acquisition and preparation of critical reagents, to monitor testing status of critical reagents, and to extract data for trend analyses.
• Contributes expertise to the development, implementation and maintenance of critical reagents inventory management and data trending tools for hands-on use by the Quality organization (e.g. QC Site Testing groups in Novato and Shanbally)
• Initiates, completes and provide SME input for Quality Management Systems (QMS) processes, such as Change Controls, Deviations, Corrective Actions and Preventative Actions (CAPAs), etc.
• Participate in projects to meet timelines to ensure on-time delivery of results and establish priorities for final reports.
• Participate in the generation of new ideas to create efficiencies and improve processes; willingly supports new ideas and process enhancements/ Engages in continuous improvement.
• Assist with regulatory and internal inspections, as needed.
• Attend team huddles, department meetings and standard work meetings as required.
• Other duties as assigned.

• Author critical reagent technical documentation, including protocols and reports for qualification, requalification, expiry extension, qualified ranges, etc.
• Perform review and data verification of technical documentation.
• Maintains critical reagent trending graphs to monitor material stability, assay performance and suitability of qualified ranges, and to support technical documentation.
• Maintains critical reagent inventory and participates in forecasting of critical reagents supply demands and identifying resupply trigger points.
• Responsible for critical reagent acquisition, preparation, qualification testing coordination and release for use.
• Coordinates and executes critical reagent distributions for the global testing network.
• Supports document authoring, data compilation and analysis for regulatory submissions (BLA, MAA, etc.) and response letters (RTQs, etc.) for commercial products.
• Utilizes LIMS to document acquisition and preparation of critical reagents, to monitor testing status of critical reagents, and to extract data for trend analyses.
• Supports development, implementation and maintenance of critical reagent inventory management and data trending tools for hands-on use by the Quality organization (e.g. QC Site Testing groups in Novato and Shanbally)
• Initiates, completes and provide SME input for Quality Management System (QMS) processes, such as Change Controls, Deviations, Corrective Actions and Preventative Actions (CAPAs), etc.
• Participate in projects to meet timelines to ensure on-time delivery of results and establish priorities for final reports.
• Participate in the generation of new ideas to create efficiencies and improve processes; willingly supports new ideas and process enhancements. Engages in continuous improvement.
• Assist with regulatory and internal inspections, as needed.
• Attend team huddles, department meetings and standard work meetings as required.
• Other duties as assigned.

• Sr. Analyst: Minimum 1 year relevant experience
• Associate 1: Minimum 3 years relevant experience
• Experience with quality management systems, current Good Manufacturing Practices (cGMP), and detailed knowledge of QC principles and compliance requirements.
• Excellent documentation, written and verbal communication skills.
• Computer literacy is required, including proficiency with Microsoft Word and Excel.
• Must have a quality service attitude and focus, exhibit flexibility and willingness to work additional hours to meet production or process requirements.

• Sr. Analyst:
• At least 2 years of relevant experience preferred
• Working understanding of analytical testing in a cGMP environment (enzymatic activity, HPLC/UPLC, cell-based bioassay, etc.)
• Associate 1:
• At least 4 years relevant experience preferred
• Experience managing cGMP critical reagent/reference standard programs
• Experience performing analytical testing in a cGMP environment (enzymatic activity, HPLC/UPLC, cell-based bioassay, etc.)
• Working understanding of sample handling and transfer in a cGMP environment
• Demonstrated working knowledge and critical thinking with respect to functional activities.
• Works with ambiguity and complexity to continuously modify options and solutions.
• Applies sound problem-solving skills to recommend options and implement effective solutions.
• Experience with Microsoft PowerPoint, Teams, Projects and/or Visio is desired.
• Familiar with relevant regulations, including 21CFR, USP, EP, and ICH requirements.

• Bachelor’s degree in a related field, or Associate’s degree with additional relevant experience

• Standard lab equipment, such as pipettes, balances, pH Meter, Biological Safety Cabinet, etc.
• Controlled Temperature Environments (CTEs), such as refrigerators and freezers
• Computer with statistical analysis and LIMS electronic softwares

• Primary working hours: Monday – Friday, day shift business hours (Pacific Time)
• Requires some flexibility to attend meetings outside of standard business hours to work with colleagues in other time zones
• Flexibility for hybrid schedule, preferred 4 days on-site

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.

The salary range for this position is: $65,600 to $90,200. BioMarin considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans.

For additional benefits information, visit: https://careers.biomarin.com/benefits.

• Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.