Our Florence (West) site specializes in process development and chemical production of intermediates and Active Pharmaceutical Ingredients (APIs) supporting toxicology, pre-clinical, and clinical supply. Operations are conducted under both non-cGMP and cGMP conditions. This site is recognized for its specialized capabilities in delivering high-quality chemical solutions across the drug development lifecycle. Discover Impactful Work: As part of our Florence (West) team, you will contribute to the development and production of critical pharmaceutical intermediates and APIs that support early-stage and clinical programs. Your work will directly impact the advancement of life-saving therapies by ensuring robust, scalable, and compliant chemical processes. You will collaborate across multidisciplinary teams to solve complex challenges and drive innovation in chemical development and manufacturing. Day in the Life: Support process development activities for intermediates and APIs Execute chemical synthesis and scale-up activities in lab and/or manufacturing environments Ensure compliance with cGMP and non-cGMP requirements as applicable Collaborate with cross-functional teams including Quality, Manufacturing, and Analytical Document experimental work, batch records, and technical reports accurately Troubleshoot process issues and identify opportunities for optimization Maintain a safe working environment and follow all safety protocols
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Job Type
Full-time
Career Level
Mid Level
Education Level
Ph.D. or professional degree