Scientist
$120,000–$127,000 year
On-siteGaithersburg, Maryland, United States
Job Summary
Oversee downstream process development for VRC clinical candidates, including tech transfer to VCMP, viral clearance validation, and toxicology lot material production. Lead troubleshooting and optimization studies using DOE with JMP to ensure product quality and recovery characteristics. Manage protocol editing, execution, and reporting while coordinating with manufacturing teams for timely technology transfer and facility fit calculations. Serve as subject matter expert for purification strategies, guide IND submissions, and mentor junior staff on laboratory instruments and research techniques. Present findings at national meetings and publish peer-reviewed manuscripts to drive innovation.
Required Qualifications
- PhD in Bioengineering, Chemical Engineering, Biochemistry, or a related discipline
- Minimum of eight (8) years of experience in recombinant protein purification development for GMP clinical-phase products
- Demonstrated knowledge of maintaining accurate and detailed records
- Must be a team player who can effectively work with members from cross-functional departments
- Strong oral and written communication skills
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