Senior Scientist, Chemical Dev & Manufacturing (Hybrid)

biomarin

Novato (CA)

Hybrid

USD 150,000 - 190,000

Full time

14 days+
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Job summary

BioMarin is seeking a Senior Scientist 2 in Chemical Development & Manufacturing to lead clinical programs and drive external manufacturing partnerships. The role emphasizes cross-functional leadership, program planning, and CDMO network management within the DST function of Technical Operations.

The candidate will manage multiple projects, contribute to budget planning, and ensure regulatory and cGMP compliance while working in a hybrid environment with travel that may be required.

Qualifications

  • Must have: Degree in Chemistry/Chemical Engineering (BS/MS/PhD).
  • Minimum 9 years in synthetic molecule, drug substance development and CMC DS programme management.
  • Knowledge of pharmaceutical regulatory requirements and cGMP.
  • Excellent written and oral communication; able to present frequently.
  • Experience managing multiple programs/projects concurrently.
  • Hybrid work: ~2 days/week on BioMarin site; 20–30% travel.

Responsibilities

  • Drive clinical programs through PPQ as a Partner Team Lead (PTL).
  • Lead CDMO network strategy and performance with internal functions.
  • Collaborate across DS, Formulation, Analytical, External Manufacturing, QA, and Supply Chain.
  • Contribute to group strategy, budgeting, and program planning.

Skills

Leadership
Project management
Cross-functional collaboration
Written and oral communication
Strategic planning

Education

Bachelor’s/Master’s/PhD in Chemistry or Chemical Engineering

Tools

ERP
Quality documentation systems

Job description

BioMarin is seeking a Senior Scientist 2 in Chemical Development & Manufacturing to lead clinical programs and drive external manufacturing partnerships. The role emphasizes cross-functional leadership, program planning, and CDMO network management within the DST function of Technical Operations.

The candidate will manage multiple projects, contribute to budget planning, and ensure regulatory and cGMP compliance while working in a hybrid environment with travel that may be required.

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