Jobs at GSK

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

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

The role involves managing maintenance teams, overseeing plant modifications, ensuring GMP compliance, and supervising technicians to achieve operational targets in the biopharmaceutical industry.

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 leading validation activities for projects, ensuring compliance with quality systems, and collaborating with cross-functional teams in the pharmaceutical sector.

Support Manufacturing Operations by managing deviation investigations, optimizing processes, and participating in technology transfers while ensuring compliance with regulations.

As a Manufacturing Engineer intern, you will supervise production activities, improve processes, and ensure compliance with safety and quality standards in the manufacturing environment.

Join the Quality Control Internship at GSK to assist in document management, laboratory operations, and improvements in a vaccine manufacturing environment.

Support the operations team in daily production activities, drive continuous improvement projects, coordinate with stakeholders, and learn fermentation and purification processes as part of a biotechnologist internship.

The Engineering Platform Lead oversees GMP compliant platforms for oligonucleotide manufacturing, ensuring quality and efficiency from development to commercial supply.

The Senior Biotechnologist oversees batch operations, prepares materials, leads equipment setup, maintains records, improves processes, and ensures compliance in biopharmaceutical manufacturing.

The Manufacturing Engineer will design and improve manufacturing processes, support project execution, and ensure compliance with safety and quality standards.

The Operations Engineer will support manufacturing operations, drive process improvements, troubleshoot issues, and collaborate on new product introductions while ensuring compliance with quality standards.

The Senior Manufacturing Engineer will enhance manufacturing processes, lead development and technology transfers, and implement improvements in chemical unit operations while collaborating across teams focusing on quality and safety.

Lead safe and efficient manufacturing operations, manage investigations, design process improvements, support technical transfers, and prepare technical documents.

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

This programme offers training in biopharmaceuticals manufacturing, focusing on process reliability, equipment troubleshooting, and project management, tailored for new graduates in engineering.

Support end-to-end production operations in a manufacturing facility, optimizing processes while adhering to cGMP requirements and safety standards.

Manage a team for instrumentation engineering projects, ensure plant modifications and maintenance comply with standards, and supervise junior staff.

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