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The Quality Assurance Specialist at Catalent is responsible for ensuring compliance with FDA regulations and internal quality systems. Key duties include managing quality assurance policies, interfacing with clients, reviewing project documents, and providing guidance on quality management systems. This role requires collaboration internally and with clients to maintain effective quality relationships and ensure product readiness for shipment.

The Associate Scientist I - Quality Control role involves executing and documenting cGMP Quality Control testing, operating laboratory equipment, performing environmental monitoring, preparing solutions, and maintaining a GMP quality system. The role is entry-level and requires training on technical procedures.

The Associate Scientist I - Quality Control will execute cGMP Quality Control testing, operate basic lab equipment, perform solution preparations, ensure adherence to GMP standards, and conduct routine Environmental Monitoring. This role requires documentation of analytical data and participation in basic laboratory maintenance tasks.

The Project Manager will lead multidisciplinary teams on complex projects, ensuring client requirements are met and milestones achieved. Responsibilities include project planning, tracking progress, managing changes, and facilitating risk assessments while ensuring effective communication with stakeholders.

The Associate Engineer in Automation Engineering will maintain and repair production and laboratory control systems, manage user accounts, troubleshoot equipment problems, support IT initiatives, and train end-users on computerized systems. This role involves teamwork on projects and ensuring compliance with health and safety standards.

The Quality Control Analyst I conducts QC testing and analytical activities, executing chemical and physical analyses of materials, compiling data for documentation, and participating in investigations and report preparations in compliance with regulations.

The Process Engineer evaluates and improves processes and equipment for efficiency and cost savings, supports project documentation, conducts risk assessments, oversees process lifecycle management, and collaborates with engineering teams for biologics manufacturing.