Research Associate 1, Process Analytics and Services (Analytical Sciences)

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.
SUMMARY
The Analytical Sciences department is seeking a Research Associate 1 to join the Process Analytics & Services (PAS) function. This is a hands-on laboratory role supporting analytical testing and characterization of therapeutic candidates across process development, early clinical, late-stage, and commercial programs.
The selected candidate will execute a variety of GxP and non-GxP analytical methods to support drug substance and drug product process development, method lifecycle activities, and cross-functional technical investigations. This role requires strong laboratory execution, data analysis, and collaboration skills in a fast-paced, multi-disciplinary environment.

KEY RESPONSIBILITIES

Analytical Testing & Data Execution
Perform routine and non-routine analytical testing to support process development (Drug Substance and Drug Product) and lifecycle programs
Execute assays including:
Chromatographic methods (e.g., HPLC/UPLC)
Capillary electrophoresis (CE) and gel-based electrophoresis (e.g., SDS-PAGE)
Spectrophotometric methods (e.g., UV/Vis, FTIR)
Plate-based assays (e.g., ELISA) and cell-based bioassays
Basic nucleic acid and compendial physicochemical testing
Accurately document test results in accordance with GMP/GLP and internal procedures
Analyze and interpret analytical data and communicate results clearly
Method Lifecycle & Laboratory Support
Support method qualification, optimization, validation, and transfer activities under supervision
Assist with drafting and updating technical documents (e.g., analytical procedures, protocols, reports)
Support troubleshooting of analytical methods and laboratory workflows
Maintain laboratory equipment and ensure readiness of reagents, standards, and materials
Process Development & Cross-Functional Support
Provide analytical testing support for process development, manufacturing, and investigation activities
Collaborate with cross-functional teams including:
Drug Substance Technologies (DST)
Formulation and Drug Product Technologies (FPT)
Manufacturing Sciences & Technology (MSAT)
Manufacturing, Quality Control, and Quality teams
Support in-process, release, and stability-related analytical testing
Compliance & Inspection Readiness
Ensure all work is performed in accordance with GxP requirements and BioMarin procedures
Maintain laboratory documentation and data in an inspection-ready state
Support regulatory inspections, audits, and site readiness activities
Data Management & Communication
Document experimental plans, results, and conclusions clearly and accurately
Maintain organized electronic records to ensure traceability and data integrity
Present data and progress updates in team meetings
Continuous Improvement & Team Support
Contribute to improvement of laboratory processes, workflows, and documentation practices
Support training and knowledge sharing within the team as appropriate
REQUIRED SKILLS
Hands-on experience with one or more analytical techniques (e.g., HPLC/UPLC, CE, ELISA, spectrophotometry)
Basic understanding of GMP/GLP principles and data integrity expectations
Ability to analyze and interpret data
Strong written and oral communication skills
Strong organizational skills with the ability to manage multiple tasks
Ability to work independently and collaboratively in a team environment
PREFERRED SKILLS
Hands-on experience with chromatographic (LC/HPLC/UPLC) and capillary electrophoresis (CE) methods
Exposure to biopharmaceutical development or protein characterization
Experience with bioassays or cell-based assays
Familiarity with analytical method lifecycle activities (e.g., qualification, troubleshooting, validation, or transfer)
Experience working in a cross-functional or fast-paced environment
EDUCATION & EXPERIENCE
Bachelor’s degree in Biochemistry, Chemistry, Biology, Analytical Chemistry, or related field
1–2 years of relevant experience in a pharmaceutical or biotechnology environment
Master’s degree is a plus but not required
ADDITIONAL INFORMATION
This is a fully onsite laboratory role
Routine work includes handling chemicals and biological materials with appropriate safety practices
May require occasional flexibility to support operational needs
EQUIPMENT
Operation of standard laboratory equipment for biochemistry and for cellular assays
REPORTING STRUCTURE
Reports to: Sr. Manager, Process Analytics & Services
No supervisory responsibilities
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law.
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.