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The Product Development Engineer II will support the development of pharmaceutical processes and lead setup and execution experiments. Responsibilities include technology transfer, data analysis, training manufacturing teams, and providing technical support across departments.

The Sr. Specialist, QA-OTF provides Quality Assurance support for GMP Manufacturing, focusing on oversight of master/working cell banks and biological products. Key responsibilities include quality floor oversight, documentation review, conducting visual inspections, performing audits, and implementing continuous improvement initiatives. This position requires collaboration with manufacturing teams and compliance with regulatory standards.

The Senior Analyst, QA is responsible for conducting investigations into critical deviations in manufacturing processes, addressing customer complaints, and collaborating with various departments to identify root causes and implement corrective actions to prevent future occurrences. They create comprehensive reports detailing their findings and work closely with operations and quality assurance teams.