Role OverviewJoin a team dedicated to advancing lifesaving and life-enhancing medicines through exceptional scientific oversight of our company's biologics portfolio from development through commercialization. Grounded in ethics, integrity, transparency, and scientific rigor, we bring together diverse perspectives to deliver transformative medicines.
What You Will Do
Validate and implement analytical methods to support release and stability testing of clinical materials. Execute Good Manufacturing Practices (GMP) activities such as release, stability, and in-process testing of Biologics Drug Substance (DS) and Drug Product (DP).
Why It Might Be a Fit
The ideal candidate brings strong technical judgment, GMP discipline, and cross-functional collaboration skills to support biologics development and commercialization.
Requirements
- Minimum of a B.A./B.S. degree in biology, biochemistry, or related scientific field
- Minimum of 3 years of relevant experience in analytical development, validation, and/or quality control
- Minimum of 1 year experience working in a GMP environment
- Experience with separation techniques such as HPLC, UPLC, CE, iCIEF, or other advanced technology
- Proficiency with data analytics
- Understanding and adherence to ALCOA principles for documentation
- Strong organizational skills and ability to manage work to meet project timelines
- Capability to work independently with minimal supervision
- Ability to identify and resolve common technical issues
- Effectively engage, communicate, and collaborate with others
Benefits
- Medical, dental, vision healthcare and other insurance benefits (for employee and family)
- Retirement benefits, including 401(k)
- Paid holidays, vacation, and compassionate and sick days
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