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The Senior Manager, QC oversees microbiological and environmental monitoring activities, ensuring routine testing of drug products and substances align with quality standards. Responsibilities include managing a team, collaborating with stakeholders, executing analytical testing, and revenue reporting.

The Senior Analyst, QA is responsible for investigating and reporting on deviations in the manufacturing process, addressing customer complaints, and ensuring compliance. This role involves collaborating with multiple departments to determine root causes, proposing corrective actions, and documenting findings. The position requires interaction with operations and quality assurance teams to manage product disposition and compliance with regulations.

The Batch Record Reviewer is responsible for reviewing GMP documentation for manufacturing processes, ensuring compliance with regulatory standards, and supporting quality improvement initiatives. This role involves evaluating documentation, overseeing batch disposition processes, communicating with cross-functional teams, and assisting with quality assurance investigations.