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

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.

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

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.

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 Senior QA Executive, oversee sterility assurance, develop quality programs, manage deviations, and ensure compliance with GMP in the pharma industry.

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

As an Associate Analytical Scientist, you will conduct analytical testing, manage equipment, document lab procedures, support method development, solve problems, and ensure compliance with safety and quality standards.

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.