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Sr. Associate Scientist
| Company | Gilead Sciences |
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| Location | San Mateo, CA, USA |
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| Salary | $126820 – $164120 |
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| Type | Full-Time |
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| Degrees | Bachelor’s, Master’s |
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| Experience Level | Mid Level, Senior |
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Requirements
- MS/MA with at least 3 years of relevant experience, or BS/BA with at least 5 years of relevant industrial experience in biologics CMC development.
- Hands-on laboratory experience required.
- Experience with formulation development, Drug Product process development, and clinical in-use evaluation for monoclonal antibodies, bispecifics, antibody-drug conjugates, fusion proteins, and other complex biologics formats strongly desired.
Responsibilities
- Design and successfully execute experiments and activities to support formulation and drug process development, including formulation development, Drug Product manufacturing process development, and clinical in-use evaluations.
- Demonstrate understanding of analytical, biophysical characterization, and process development techniques; lead by example for lab executions.
- Clearly, timely, and accurately document data in appropriate repositories such as lab notebooks, reports, protocols, etc. following good documentation practices.
- Author technical documents such as protocols, reports, regulatory dossier, etc. and prepare data-focused presentations for internal and external audience.
- Effectively collaborate with both internal and external stakeholders in project meetings.
- Analyze data and draft conclusions before discussing with manager or supervisor.Support or represent function and work collaboratively on cross-functional teams to support project team strategy and regulatory filings.
- Fully embrace a lean-agile mindset, matrix working environment, and continuous improvement.
- Help support key project or department stakeholders as needed to ensure that company objects are met.
- Support team initiatives to drive business process excellence, scientific innovation, laboratory and work safety, etc.
Preferred Qualifications
- Experience with formulation development, Drug Product process development, and clinical in-use evaluation for monoclonal antibodies, bispecifics, antibody-drug conjugates, fusion proteins, and other complex biologics formats strongly desired.
