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Manage production activities for bulk drug substances ensuring compliance with quality and safety regulations, while leading and developing a team.

Participate in support and optimization of biopharmaceutical manufacturing processes, ensuring compliance with cGMP requirements and facilitating process improvement initiatives.

The Biotechnologist will support production operations, optimize resources, adhere to cGMP, assist in training, ensure quality compliance, and improve processes.

This role involves providing technical and business analysis for MES applications, managing deployment, testing, validation, and improving manufacturing processes.

Lead engineering activities for equipment maintenance and capital projects, ensuring compliance and mentoring junior staff in a regulated environment.

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

The internship involves maintenance of equipment, project management, equipment troubleshooting, and continuous improvement in a vaccine manufacturing environment.

As an Engineering and Compliance intern at GSK, you will assist in equipment troubleshooting, qualification, and SOP revision related to vaccine manufacturing, while gaining valuable hands-on experience.

Intern will assist in managing Quality Control projects, support data extraction and analysis, and collaborate with varying teams for compliance with regulatory standards.

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