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The Senior Scientist in Quality Control will oversee testing of samples, review contract testing invoices, analyze and interpret testing results, ensure compliance with regulatory requirements, develop product specifications, and lead continuous improvement initiatives. Responsibilities include authoring technical documents, managing quality control processes, and representing QC as a subject matter expert.
The Associate Principal Scientist in Process Development will lead scientific research for innovation in protein purification and clinical manufacturing, execute experiments using various chromatography techniques, and develop and validate new processes. The role involves writing SOPs, analyzing complex data with statistical software, and mentoring interns while ensuring project timelines are met.
The Program Manager will manage client Process Development and GMP Manufacturing projects, ensuring they meet objectives for time, budget, and quality. Responsibilities include applying project management practices, communicating effectively with clients, troubleshooting problems, and leading cross-functional teams to deliver successful results.
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 Global Lean Leader at Catalent drives the implementation of lean methodologies across manufacturing sites for continuous improvement. Responsibilities include leading workshops, performing in-depth analyses, supporting site integrations, and coaching teams on lean six sigma tools. This role demands significant travel and leadership in improving key performance metrics.
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.
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