- Monitor commercial parenteral product stability studies
- Execute stability protocols and studies using the Laboratory Information Management System (LIMS)
- Manage modifications to existing stability studies
- Coordinate and complete stability studies within defined timelines
- Provide analytical support and data for Manufacturing Investigations
- Ensure safety practices in the QC Lab stability program
- Adhere to global quality standards and regulatory requirements
- Support general sample management and laboratory operations
- High School diploma, preferred Associates or Bachelor's degree in a relevant scientific field
- Minimum 1 year of GMP Laboratory experience
- Familiarity with analytical testing and laboratory IT systems
- Ability to contribute to multiple projects and problem-solving skills
- Strong communication and collaboration skills
- Previous experience with stability study planning and execution is a plus
- Ability to work 8-hour days Monday through Friday
- Overtime may be required
- Minimal travel and on-call support
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QCL Stability Admin Tech - Durham, United States - Eli Lilly and Company
Description
Lilly - QC Stability Technician
At Lilly, we bring together care and innovation to enhance the lives of people worldwide. As a leading global healthcare company based in Indianapolis, Indiana, we are dedicated to discovering and providing life-changing medications, advancing disease management, and giving back to communities through philanthropy and volunteer work. Our priority is putting people first, and we are seeking individuals who are passionate about making a positive impact globally.
Key Responsibilities:
Basic Qualifications/Requirements:
Additional Information:
Lilly is an equal opportunity employer that values diversity and inclusion in the workplace. Join our employee resource groups to network and grow professionally. Discover more about our diverse groups and be part of our mission to make a difference.
