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Design, improve, and support manufacturing processes while collaborating with various teams, troubleshooting issues, and providing training and technical guidance.

Assist in improving manufacturing processes through data analysis, implementing Lean principles, collaborating with departments, and supporting various project initiatives.

Lead quality activities for small molecule R&D, ensuring compliance with GMP and regulatory standards, managing audits, documentation, and risks, while fostering a culture of continuous improvement.

As Site Procurement Specialist, you will drive procurement initiatives, manage supplier relationships, ensure compliance, and identify process improvements across multiple categories.

Assist in process improvement, data analysis, project support, documentation, and collaboration with different departments in vaccine manufacturing.

The internship involves supporting operational excellence activities, continuous improvement using Lean Six-Sigma, driving projects, and developing solutions for Smart Manufacturing.

The role involves ensuring compliance with quality standards in biopharmaceutical manufacturing, providing QA consultation, managing KPIs, and implementing compliance initiatives.

The internship involves supporting daily production activities, participating in commissioning processes, coordinating with stakeholders, driving improvement projects, and revising operational documents.

Traineeship QA Operations role supporting cGMP compliance in vaccine manufacturing: perform QA checks, review and approve batch records and quality documentation, assist investigations, CAPA and change control, perform audits and risk assessments, and support product quality activities.

The role involves supervising and optimizing manufacturing processes, ensuring compliance with cGMP standards, and supporting quality investigations while documenting procedures and improvements.