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

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.

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

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

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

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

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

Contribute to improvement of laboratory processes, workflows, and documentation practices

Support training and knowledge sharing within the team as appropriate

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

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

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.

The salary range for this position is: $72,000 to $99,000. 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.