Manage a team to implement site reliability strategies, ensuring plant availability by analyzing incidents, recommending maintenance strategies, and collaborating with engineers and operational teams.

The Head of MSAT is responsible for leadership in manufacturing science and technology, process validation, product lifecycle management, and enhancing production efficiency, compliance, and safety within the GSK site.

The Site Quality Director oversees all quality functions at the site, ensuring compliance with regulations, engaging the quality team, and driving continuous improvement in quality processes.

The role involves ensuring compliance with cGMP in manufacturing, conducting quality assurance checks, authorizing process orders, and reviewing documentation related to production. The candidate will also engage in risk assessments and support site investigations, while gaining insights into the GSK culture and developing soft skills.

The role involves performing operation and maintenance of utility systems, ensuring automation systems' reliability, supporting project modifications, and providing engineering qualification and validation life cycle support in a biopharmaceutical manufacturing setting.

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 Environmental Sustainability Intern, you will engage in projects focused on sustainability initiatives, including energy reduction, waste management, and climate impact assessment. You will participate in data collection and analysis, support certification preparation, and gain practical experience in project management and engineering concepts.

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 Operations Engineer is responsible for supporting Manufacturing Operations by managing deviation investigations, executing improvement initiatives, and ensuring compliance with cGMP requirements. They will also engage with various teams for process optimization and technology transfer while leading projects and utilizing available resources effectively.

The TnP Trainee - QA GMP Executive will support compliance in manufacturing operations, perform QA checks, authorize processes, review and approve documentation, and assist in investigations and internal audits to ensure cGMP compliance. The position involves extensive collaboration with manufacturing personnel and requires knowledge of FDA/EU regulatory guidelines.

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.

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.

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.

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.

Support engineering and project management in site capital project implementation, developing technical specifications, ensuring safety and compliance, managing project performance, and facilitating communication among stakeholders.

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.

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.