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The Senior Process Engineer will oversee technology transfer, process optimization, compliance, and documentation in the CGT division, ensuring GMP standards and collaborating with teams and clients.

As a Biotechnologist, you'll support GMP manufacturing of therapeutic proteins by operating mammalian cell cultures, performing downstream purification, and maintaining cGMP standards.

Lead technology transfer of manufacturing processes, provide technical oversight during GMP runs, and drive continuous improvements. Collaborate across teams and support regulatory inspections.

The QA Expert will oversee Quality Assurance activities, support audits, lead projects, and mentor junior team members within a GxP manufacturing environment.

Provide QA oversight for multi-product GMP biopharma manufacturing: review batch records, approve SOPs/protocols, lead small team and projects, manage deviations, change controls, CAPA, audits, and support regulatory inspections.

The QA Trainee will support Quality Assurance activities, manage GMP documents, provide compliance support, and uphold data integrity.

Lead a technical team in bioprocessing, manage client relationships, support product integration into therapy development, and deliver presentations for industry engagement.

The Biotechnologist Trainee will perform GMP manufacturing tasks, including equipment monitoring, basic laboratory procedures, and maintaining cleanroom standards while working under supervision.

The QC Analyst will conduct analytical testing, document results, troubleshoot methods, support lab operations, and ensure compliance with quality systems.

The Technical Specialist is responsible for managing manufacturing operations, including operational readiness, deviation investigations, and supporting continuous improvement initiatives.