Glycan Analytics & Biophysical Assays Scientist

Initial Therapeutics, Inc.

Novato (CA)

On-site

USD 120,000 - 170,000

Full time

14 days+
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Job summary

BioMarin Pharmaceutical Inc. is seeking a Scientist 2 to lead glycan-focused analytical method development and transfer within the Analytical Sciences team in Novato, CA.

You will collaborate with cross-functional teams across Process Development, Formulation Development, Quality, Regulatory Affairs, and Research to advance DS/DP characterization and regulatory readiness. The role requires hands-on LC-MS, HILIC, CE/icIEF, RP, SEC, IEX expertise, with strong communication skills and adaptability

Qualifications

  • Glycan characterization and analysis expertise with method development.
  • Experience with LC-MS, CE, cIEF/icIEF, HILIC-FLD/MS.
  • Knowledge of DS/DP formulation development and regulatory readiness.

Responsibilities

  • Lead analytical method development and transfer for DS/DP across clinical and commercial programs.
  • Support IND/BLAs by writing analytical sections and responding to agency questions.
  • Develop and optimize chromatography, spectroscopy, and MS-based methods for glycan analysis.
  • Prepare, review, and approve analytical protocols and reports.
  • Document experiments and results for audits and inspections.
  • Maintain lab and instrument readiness; support general maintenance.
  • Mentor junior scientists and research staff.

Skills

Glycan characterization
LC-MS
HILIC
CE-based methods
IEX
RP chromatography
Mass spectrometry
Analytical method development
Regulatory submissions support

Education

PhD in Chemistry, Biochemistry, pharmaceutical chemistry or related field
MSc in Chemistry, Biochemistry, pharmaceutical chemistry or related field

Tools

LC-MS
SEC
IEX
RP chromatography
HILIC

Job description

BioMarin Pharmaceutical Inc. is seeking a Scientist 2 to lead glycan-focused analytical method development and transfer within the Analytical Sciences team in Novato, CA.

You will collaborate with cross-functional teams across Process Development, Formulation Development, Quality, Regulatory Affairs, and Research to advance DS/DP characterization and regulatory readiness. The role requires hands-on LC-MS, HILIC, CE/icIEF, RP, SEC, IEX expertise, with strong communication skills and adaptability

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