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.

The Quality Validation Officer ensures product compliance with cGMP and regulatory standards, drafts policies, conducts reviews, and manages validation processes at the manufacturing site.

The trainee will ensure cGMP compliance in manufacturing, conduct quality checks, authorize documentation, and support quality investigations in the biopharmaceutical sector.

As a Biotechnologist, you will assist in the production of bulk drug substances by adhering to safety and cGMP standards, maintaining cleanliness in facilities, and operating various equipment.

Support analytical activities for vaccines, focusing on equipment setup, method validation, data management, and ensuring compliance with safety and quality standards.

You will support the GSK Production System team by collecting data, driving improvement projects, and assisting in workshops to enhance continuous improvement culture.

As an intern, assist with planning, execution, and monitoring of technology projects in biopharma, perform data analysis, and manage documentation.

Assist in smart manufacturing projects focusing on automation and digital solutions. Involves data collection, analysis, and creating dashboards. Gain insights into production and operational excellence.

Assist in engineering support for the new HBV vaccine facility, including qualification activities, documentation, and project responsibilities while gaining hands-on experience in biopharmaceutical manufacturing.

The intern will assist the QA GMP team, support day-to-day activities, manage records and trackers, and develop training materials.

Assist with productivity improvement projects in API manufacturing while gaining hands-on experience in various engineering disciplines. Learn about Good Manufacturing Practices and contribute to automation and process optimization.

Assist in ensuring compliance with GMP regulations by analyzing and testing raw materials and products, maintaining lab equipment, and troubleshooting issues.

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

The intern will support manufacturing engineers by optimizing production processes and improving product yield while gaining hands-on experience in troubleshooting, lean tools, and data analysis.

As a Digital Data Analytics Intern, you will support data scientists and manage operational data to build predictive models. Responsibilities include developing dashboards and participating in business use cases with engineers and chemists.

The UI/UX Developer Intern will enhance the user experience of a data science platform by designing interfaces, conducting usability testing, and collaborating with teams to implement improvements.

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

The Operations Engineer supports manufacturing operations by resolving process issues, leading improvement projects, and ensuring compliance with quality standards.

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

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