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The Development Scientist II is responsible for pharmaceutical development and clinical manufacturing project activities, including formulation and process development, GMP compliance, budget planning, customer interaction, and documentation writing. The role involves assisting with batch manufacturing and problem-solving in formulation processes while ensuring accuracy and compliance with guidelines.

The Principal Continuous Improvement Engineer will lead CI initiatives at a manufacturing facility for gene therapies. Responsibilities include identifying improvement opportunities, facilitating problem-solving, coaching project leaders, and promoting a Continuous Improvement culture. This is a full-time on-site position at the Harmans/BWI campus, focusing on quality, compliance, and patient safety.

Quality Control Analyst responsible for executing QC testing and analytical activities supporting product development, release, and stability. Conducts chemical and physical analyses, compiles data, participates in investigations, and reviews data for compliance. Operates analytical instrumentation, monitors equipment, and assists in SOP construction and updating. Bachelor's degree in Physical or Chemical Sciences with 2+ years of experience in a GMP environment required.