Principal Scientist, Analytical Lifecycle Management
Gilead SciencesUnited States - California - Foster City · Principal
$195,670 – $253,220
Listed on Gilead Sciences’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role leads quality control strategy for late-stage biologic drug development, serving as the primary QC representative on cross-functional teams responsible for analytical methods, regulatory submissions, and commercialization readiness. It suits experienced analytical or quality professionals with deep biologics expertise who can independently drive complex QC decisions and mentor others in a matrix environment.
Our summary, not Gilead Sciences’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- PhD in Chemistry, Biochemistry, Pharmaceutical Sciences, Biological Sciences or related discipline with 5+ years relevant experience, OR Master's degree with 8+ years experience, OR Bachelor's degree with 10+ years experience
- Quality Control, Analytical Development, or CMC technical leadership in biologics programs
- Independent decision-making on complex QC and compliance issues
- Cross-functional influence and stakeholder communication
Nice to have
- Extensive late-stage biologics QC strategy experience including method establishment, validation, transfer, and specification setting
- Deep understanding of global GMP expectations and ICH guidance for biologics
- Experience authoring or reviewing regulatory submissions and CMC documentation
- Oversight of CDMOs and contract testing laboratories
- Mandarin language proficiency