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Sr Research Associate II

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BioMarin Pharmaceutical

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Location:
United States , Novato

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Category:
Research and Development

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Contract Type:
Contract work

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Salary:

31.00 - 50.00 USD / Hour
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Job Description:

The selected candidate will work in the Separations and Biophysical Assays team within the Analytical Sciences group to assist in the advancement of BioMarin's therapeutics for clinical evaluation and potential commercialization. The candidate will be responsible for method development (separations), provide routine testing and characterization support to partner groups to help with early candidate selection, process development, and drug substance and drug product process characterization.

Job Responsibility:

  • Support the Separations and Biophysics group within Analytical Sciences
  • Be a hands-on presence in the laboratory, supporting biophysical/ biochemical assay development and qualification using HPLC and CE for various modalities
  • Provide routine analytical characterization & testing support to partner groups including Upstream and Downstream PD, Formulations, and Research & Early Development (RED)
  • Document experimental results in the company electronic lab notebook (Benchling), author procedures, and contribute to technical documentation
  • Actively participate in the operational aspects of the laboratory by conducting safety inspections, lab organization, ordering supplies, and performing routine equipment maintenance
  • Present scientific literature and results from ongoing studies at group meetings and other discussion forums at the company

Requirements:

  • Bachelor’s degree in Chemistry, Biochemistry, Analytical Chemistry, Chemical Engineering or a related field with 6+ years of experience in a Biologics or Pharmaceutical environment
  • Master’s degree in Chemistry, Biochemistry, Analytical Chemistry, Chemical Engineering or a related field with 4+ years of experience in a Biologics or Pharmaceutical environment
  • Hands-on experience in the biotechnology industry or academic setting with a broad range of analytical techniques focused on analytical testing and characterization for proteins, peptides, and protein-conjugates
  • Experience with biochemical characterization methods: SEC, SCX, RP-HPLC (Agilent/Waters/Thermo LC instruments)
  • Capillary Electrophoresis (PA800 or BioPhase8800) based methods (SDS for size separation, glycan profiling)
  • Technical understanding of all aspects of analytical testing, phase appropriate regulatory requirements, method qualifications, and method transfers
  • Ability to independently troubleshoot issues, ideate, and develop insights into technical challenges and propose solutions
  • Demonstrates attention-to-detail and “right-the-first time’ approach
  • Excellent written and oral communication skills
  • Ability to influence others effectively and develop collaborative relationships
  • Familiar with use of statistical software, electronic document management, and laboratory information management
  • Ability to effectively analyze complex problems and present results
  • Ability to flexibly adapt to changing business needs and meet timelines
  • Strong organizational skills with the ability to effectively multi-task and prioritize

Nice to have:

  • cIEF (Maurice) experience
  • LC-MS (Orbitrap/QToF/QQQ) method development experience
  • Experience in method development, qualification, and transfer to/from other laboratories such as development, quality control
  • Knowledge of biopharmaceutical process development
  • Experience with automation
  • Experience working in a cross-functional environment
  • Good understanding of root cause analysis methodology
What we offer:
  • Discretionary annual bonus
  • Discretionary stock-based long-term incentives
  • Paid time off
  • Company-sponsored medical, dental, vision, and life insurance plans

Additional Information:

Job Posted:
March 19, 2026

Employment Type:
Fulltime
Work Type:
On-site work
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