Support daily production activities in the Vaccines Business Area, assist in operational improvements, manage stakeholders, and perform cleaning and calibration tasks.

The role involves assisting in project delivery by engaging with multidisciplinary teams, ensuring compliance with safety and quality standards, and managing project performance.

As a QC intern, you'll manage documents, perform laboratory operations, and learn about GMP requirements while contributing to quality control in vaccine manufacturing.

As a QC intern, you'll learn about processes in the QC department, manage documents, support QC activities, and perform data tabulation and trending for quality control tests.

The role involves QA oversight, supporting investigations and audits, coaching teams, ensuring compliance with GMP, and engaging with production.

The role involves supporting manufacturing operations including managing deviations, process improvements, and ensuring compliance with quality guidelines. You will engage in training and project management, working closely with various departments to achieve production objectives.

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 ensure production quality and timing of bulk drug substances, maintain equipment, and contribute to continuous improvement. Responsibilities include compliance with cGMP, documentation, training, and operational support.

Act as microbiology expert, ensure compliance with regulations, conduct audits, develop strategies for environmental monitoring, and support investigations of microbiology-related issues.

As a Biotechnologist, you will assist in drug production processes, maintain equipment, ensure safety compliance, and support facility monitoring and housekeeping tasks.