Senior Associate Scientist, Biologics Formulation

Gilead Sciences Inc.; Maryland; On-site; USD 127,000 - 164,000; Full time

Benefits offered by this job

Discretionary bonus

Stock-based long-term incentives

Paid time off

Benefits package

Job summary

Gilead Sciences Inc. is seeking a Sr. Associate Scientist in Biologics Pivotal & Commercial Formulation and Process Development to contribute to formulation and drug product processes for innovative molecules advancing medicines into the clinic.

The role emphasizes hands-on laboratory work, data interpretation, and collaboration with cross-functional teams to support regulatory filings and development milestones, with competitive compensation and benefits.

Qualifications

• MS/MA with 4+ years, or BS/BA with 6+ years in biologics CMC development.
• Hands-on laboratory experience required.
• Experience with formulation development and Drug Product processes preferred.
• Experience with monoclonal antibodies, bispecifics, ADCs and other complex biologics formats is strongly desired.

Responsibilities

• Design and execute experiments to support formulation and drug product process development.
• Demonstrate understanding of analytical and biophysical characterization techniques and lead lab executions.
• Document data accurately in notebooks, reports, and protocols following good documentation practices.
• Author technical documents and prepare data-focused presentations for internal and external audiences.
• Collaborate with internal and external stakeholders in project meetings and regulatory filings.

Skills

Hands-on laboratory experience

Education

MS/MA with 4+ years, or BS/BA with 6+ years in biologics CMC development

BS/BA with 6+ years in industrial experience

Job description

Gilead Sciences Inc. is seeking a Sr. Associate Scientist in Biologics Pivotal & Commercial Formulation and Process Development to contribute to formulation and drug product processes for innovative molecules advancing medicines into the clinic.

The role emphasizes hands-on laboratory work, data interpretation, and collaboration with cross-functional teams to support regulatory filings and development milestones, with competitive compensation and benefits.