gilead
Senior Associate Scientist, Purification Process Development
At a Glance
- Location
- United States - California - Foster City, United States
- Work Regime
- onsite
- Employment
- Full time
- Experience
- 3+ years
- Compensation
- y range for this position is: $126,820.00 - $164,120.00. Gilead considers a variety o
- Posted
- 2026-08-14
Key Requirements
Required Skills
Certifications
- GMP
Domain Knowledge
- Automation
- Engineering
- Insurance
- Manufacturing
- Medical
Benefits & Perks
aid time off, and a benefits package. Benefits include company-sponsored med
Requirements
with 5+ years industrial experience in biologics purification development.
Hands-on laboratory operations experience bench and pilot scale chromatography, TFF, VF and depth filtration.
Experience in pre-pivotal stage purification process development, scaleup and implementation in GMP and non GMP manufacturing facilities.
Experience in statistics, design-of-experiments, and data analysis (e.g.
Working knowledge of lab automation, data management, data science, knowledge management and data protection.
Knowledge in single-use manufacturing technology and cGMP guideline is a plus.
Responsibilities
Establish and maintain a state-of-the-art purification lab that enables rapid new biologics entities manufacturability assessment, purification process development and scaleup.
Contribute to experimental design.
Plan and execute purification process development laboratory studies independently.
Support process scaleup and implementation in internal and external GMP facilities.
Collect and analyze data from laboratory experiments in compliance with data integrity policy.
Author and review experimental protocols and reports.