Specific Job Responsibilities:
- May plan and conduct method validation and transfer experiments for clinical and commercial drug substances and products.
- Conducts GMP testing for release and stability of clinical drug substances and products using various analytical techniques.
- Applies knowledge and complies with GMP in daily activities.
- Conducts GMP data review to ensure compliance with applicable Standard Operating Procedures (SOPs), test methods, specifications, and protocols.
- Performs regulatory filing analytical data verification to ensure data integrity.
- Conducts experiments for troubleshooting failures/investigations under limited supervision.
- Authors and reviews analytical test methods, supporting documents, validation or transfer protocols and reports.
Specific Education & Experience Requirements:
- 4+ years of experience with a BA or BS degree in Chemistry or Biology.
OR
- 2+ years of experience with an MS degree in Chemistry or Biology.
General (Skills/Behavior):
- Applies Gilead Core Values and Leadership Commitments to job responsibilities.
- Demonstrates good verbal communication skills and interpersonal skills.
- Works with collaborative communication and a problem-solving spirit.
- Works with minimal supervision on projects of basic to moderate complexity.
Benefits (explicitly stated):
- Company-sponsored medical, dental, vision, and life insurance plans; discretionary annual bonus and discretionary stock-based long-term incentives; paid time off; eligible employees may participate in benefit plans.
Application Instructions:
- Please apply via the Internal Career Opportunities portal in Workday.