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The role involves providing QA oversight in a GMP facility, reviewing and approving documentation, leading deviations and CAPAs, troubleshooting quality issues, and ensuring process improvements and compliance.

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

As a Technical Expert, lead manufacturing projects in cell and gene therapy, ensure compliance with cGMP, and drive cross-functional improvements.

The Biotechnologist Trainee is responsible for manufacturing therapeutic proteins under cGMP conditions, performing lab tasks, equipment monitoring, and maintaining high facility standards while learning strict manufacturing protocols.

In this role, you will perform GMP manufacturing operations, handle equipment, maintain lab standards, and apply aseptic techniques in a team-oriented environment.