The Senior Biotechnologist will oversee the set-up of production operations, ensuring efficiency and compliance with quality and safety regulations. Responsibilities include media preparation, manufacturing of drug substances, commissioning activities, continuous improvement initiatives, documentation, training, and interfacing with other departments.

The internship involves supporting engineers in assignments, shadowing operations, continuous improvement initiatives, data compilation for equipment performance, and assisting in equipment qualification. Interns will also learn about Good Manufacturing Practices and workflow mapping while working in a cleanroom environment.

As an Operations Engineer, you will provide technical support to Manufacturing Operations, focusing on process optimization, validation, and continuous improvement initiatives while ensuring compliance with cGMP requirements. You'll manage investigations, track process parameters, and support project execution, alongside guiding team members.

The Automation Engineer is responsible for implementing plant modifications, supporting compliance and validation processes, managing and troubleshooting DCS/PLC systems, and ensuring regulatory standards are met. They will also participate in audits and support preventive maintenance and project management efforts.

The Quality Assurance (QA) GMP Internship at GSK involves supporting the QA team with various tasks such as scanning and archiving batch records, performing quality improvement projects, and maintaining trackers. Interns will gain valuable experience in vaccine manufacturing and contribute to projects that positively impact health.

As a Technical Services Engineer Intern, you will provide engineering support for the new Hepatitis B vaccine facility, assist in qualification activities, perform documentation reviews, support asset care programs, and collaborate with local and global engineering teams.

Interns will assist in planning and executing culture and communications programmes at GSK, supporting communication events and activities, developing communication assets, and engaging with stakeholders to promote internal communication efforts.

Interns will work with the Culture and Communications Lead to plan and execute communication programs, support events, develop communication assets, produce engaging stories, and analyze content engagement. They will gain skills in stakeholder management and internal communication strategies while working in a collaborative environment.

The role involves assisting project managers with site capital project implementation, ensuring compliance with safety and regulatory standards, managing project performance, and supporting communication and planning for project benefits. The trainee will learn project execution and management skills, along with effective communication and analytical abilities.

The MSAT Product Specialist role involves managing and improving processes to ensure product quality in biopharmaceutical manufacturing. Responsibilities include process verification, data analysis, corrective actions, audit preparation, and project management, focusing on lifecycle management and customer impact.

As an intern in the Digitalization & Innovation team, you will assist in developing manufacturing processes, support project teams with electronic batch records, collaborate with users to capture requirements, and promote MES awareness through content creation. You'll gain hands-on experience with MES technology and insights into biopharmaceutical manufacturing practices.

The Senior QA Executive assists in managing quality systems in compliance with GSK standards and cGMP regulations. Responsibilities include overseeing document archival, consulting on quality assurance issues, and managing training metrics. They ensure compliance with regulatory requirements and perform annual system reviews.

The role involves ensuring cGMP compliance in manufacturing operations, conducting QA checks, managing documentation, and supporting investigations related to quality. Trainees will gain hands-on experience and learn about regulatory guidelines while interacting with a diverse team.

As a UI/UX Developer Intern, you will enhance the UI/UX of a data science platform by implementing design improvements, conducting usability tests, and collaborating with teams to optimize user experience.

This internship involves working with the production team to learn about Active Pharmaceutical Ingredients manufacturing and participating in key improvement projects. Interns will focus on productivity initiatives, automation, data analysis, and process optimization, while developing key project support skills.

Assist in the yield improvement of vaccine manufacturing through data analysis, support initiatives, and maintain documentation. Collaborate with teams to communicate findings and participate in discussions on process optimization. Gain hands-on experience and mentorship.

The Senior Operations Supervisor leads a team of biotechnologists in executing process operations, ensuring timely batch completion. Responsibilities include managing team morale, overseeing production performance, ensuring compliance with quality standards, and providing training and development for staff. The role requires effective troubleshooting and management skills to foster a continuous improvement environment.

Interns will assist in Quality Checks projects, ensuring manufactured products meet regulatory standards, and support data extraction and analysis. Key responsibilities include collaboration with various teams and gaining experience in a GMP environment.

The role involves overseeing quality assurance in biopharmaceutical manufacturing, ensuring compliance with regulations, conducting QA checks, reviewing documentation, and supporting investigations and audits. Trainees will receive training to develop skills in quality assurance and manufacturing processes while adhering to EHS standards.

The Operational Quality Specialist ensures compliance with cGMP and regulatory requirements while overseeing manufacturing operations. Responsibilities include reviewing and approving documentation, conducting audits, supporting quality oversight during operations, and coordinating periodic reviews of products and systems.