A company is looking for a Contract Associate in Analytical Chemistry, Project Management & Clinical Supply.
Key Responsibilities :
Track and manage analytical development timelines, deliverables, and cross-functional dependencies
Coordinate with internal teams and external partners to ensure timely execution of project milestones
Support planning of clinical supply timelines and ensure compliant delivery of clinical trial supplies
Required Qualifications :
Bachelor's or Master's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field
7+ years of experience in the pharmaceutical or biotechnology industry, preferably in CMC or analytical development
Hands-on project management experience in a cross-functional environment
Familiarity with analytical techniques and regulatory expectations for CMC submissions
Understanding of clinical supply chain processes and GMP requirements for drug product release
Analytical Chemistry • Ontario, California, United States