Empower our bioanalysis team by independently designing and executing LC-MS projects. Contribute your expertise with biologics and small molecules in a dynamic lab environment focused on advancing drug development timelines and goals.

Join a team that's establishing quality assurance systems in a GMP environment, ensuring compliance and excellence in oral solid dosage and sterile drug manufacturing. Help shape a culture of 'Right First Time' through independent quality oversight and collaboration.

Join as a QC Laboratory Operations Lead to manage stability, sample lifecycle, and lab systems in a fast-paced GMP environment, ensuring compliance and operational excellence while fostering team development and continuous improvement.